Advances in Development of Radiometal Labeled Amino Acid-Based Compounds for Cancer Imaging and Diagnostics

Radiolabeled biomolecules targeted at tumor-specific enzymes, receptors, and transporters in cancer cells represent an intensively investigated and promising class of molecular tools for the cancer diagnosis and therapy. High specificity of such biomolecules is a prerequisite for the treatment with a lower burden to normal cells and for the effective and targeted imaging and diagnosis. Undoubtedly, early detection is a key factor in efficient dealing with many severe tumor types. This review provides an overview and critical evaluation of novel approaches in the designing of target-specific probes labeled with metal radionuclides for the diagnosis of most common death-causing cancers, published mainly within the last three years. Advances are discussed such traditional peptide radiolabeling approaches, and click and nanoparticle chemistry. The progress of radiolabeled peptide based ligands as potential radiopharmaceuticals is illustrated via novel structure and application studies, showing how the molecular modifications reflect their binding selectivity to significant onco-receptors, toxicity, and, by that, practical utilization. The most impressive outputs in categories of newly developed structures, as well as imaging and diagnosis approaches, and the most intensively studied oncological diseases in this context, are emphasized in order to show future perspectives of radiometal labeled amino acid-based compounds in nuclear medicine.


Introduction
Over past 20 years, in the field of nuclear medicine, substantial progress has been made in the development of novel radiopharmaceuticals and radiolabeled agents for diagnosis and therapy of various diseases. Nowadays, a great emphasis is put on a synthesis and study of radiolabeled amino acid-derived biomolecules with a selective distribution and binding to target structures in living cells and tissues, i.e., enzymes, transporters, or peptide receptors. This allows targeted therapy and diagnostic evaluation of pathological changes in many fields, such as oncology, neurology, endocrinology, cardiology, and also investigation of inflammation processes or infection.
Especially, malignant tumor diseases are of the biggest interest because of their increasing global incidence, and placing second in the causes of death. The effect of target-specific radiolabeled compounds is often mediated through binding with high affinity to specific protein structures (e.g., active places in enzymes or receptors). Many of these structures are overexpressed in diseased cells compared to their absence or lower density under physiological conditions. Since that, such radiolabeled compounds represent effective probes in a recognizing and visualizing tumor cells in their early stage. All types of malignant solid tumors often exhibit lower oxygenation levels than their original tissues resulting in a hypoxic state, which impacts on the reduced effectiveness of tumor therapy and propagation of metastasis. Hence, there is an urgent need to enhance detection approaches for monitoring various tumor types, including hypoxic cancer lesions. In this field, amino acid-based target-specific radiopharmaceuticals have become significant tools in modern oncology allowing cancer imaging on molecular and cellular level [1].
In order to utilize biomolecules for imaging and diagnosis, they must be properly labeled. Metal radionuclides belong to the most powerful and the most employed labels in nuclear medicine. In the group of metallic radioisotopes, gamma and positron emitters, namely copper-62, copper-64, gallium-67, gallium-68, indium-111, and technetium-99m have proved to be the most suitable for nuclear research and clinical application [2,3]. Apparently, other potential radionuclides such as zirconium-89, yttrium-86, and cobalt-55 have been included in recent studies since these have become more readily available with high purity. A diversity of synthesis strategies, radiolabeling approaches, modified chelators, and linkers has been investigated and developed to reach the optimized targetspecific radiolabeled compounds, with proper characteristics for cancer imaging and therapy. All of these crucial components of radiolabeled compounds are the subject of many review papers, with a focus on the chemistry of metallic radionuclides [4][5][6], chelators, and linkers [7][8][9][10][11][12], as well as onco-specific peptidic biomolecules [2,[13][14][15][16].
The aim of this review is to summarize and critically evaluate state-of-the-art approaches and the most significant outputs related to the development of target-specific radiometal labeled biomolecules for imaging of severe tumor types and tumors with an increased incidence. Recent advances in synthetic approaches and radiometal-labeling strategies of amino acid-based biologically active molecules, including most employed peptide families and receptors such as somatostatin, cholecystokinin/gastrin, bombesin, integrins, and hypoxia endogenous markers, as well as inhibitors of prostate-specific membrane antigen and fibroblast activation protein, are highlighted in order to demonstrate perspectives in cancer diagnostics with amino acid-based radiopharmaceuticals.

Basic Characteristics of Conventional Metal Radionuclides and Chelators Currently Used in Nuclear Medicine
Radiometallic compounds with targeted biodistribution and binding in the human body (i.e., target-specific) include in their structure: (i) biomolecules as a crucial biodistribution component (specific to receptor); (ii) a linker as a connecting component preserving specificity of biomolecule when attaching; (iii) a bifunctional chelating agent (BFCA); and (iv) metal radionuclides (see Figure 1). Basic characteristics of the most important or most frequently used representatives in the group of conventional metal radionuclides and BFCA are briefly discussed in Sections 2.1 and 2.2, respectively. Discussion is led in general point of view or, if appropriate, with respect to amino acid based biomolecules. tissues resulting in a hypoxic state, which impacts on the reduced effectiveness of tumor therapy and propagation of metastasis. Hence, there is an urgent need to enhance detection approaches for monitoring various tumor types, including hypoxic cancer lesions. In this field, amino acid-based target-specific radiopharmaceuticals have become significant tools in modern oncology allowing cancer imaging on molecular and cellular level. [1] In order to utilize biomolecules for imaging and diagnosis, they must be properly labeled. Metal radionuclides belong to the most powerful and the most employed labels in nuclear medicine. In the group of metallic radioisotopes, gamma and positron emitters, namely copper-62, copper-64, gallium-67, gallium-68, indium-111, and technetium-99m have proved to be the most suitable for nuclear research and clinical application [2,3]. Apparently, other potential radionuclides such as zirconium-89, yttrium-86, and cobalt-55 have been included in recent studies since these have become more readily available with high purity. A diversity of synthesis strategies, radiolabeling approaches, modified chelators, and linkers has been investigated and developed to reach the optimized target-specific radiolabeled compounds, with proper characteristics for cancer imaging and therapy. All of these crucial components of radiolabeled compounds are the subject of many review papers, with a focus on the chemistry of metallic radionuclides [4][5][6], chelators, and linkers [7][8][9][10][11][12], as well as onco-specific peptidic biomolecules [2,[13][14][15][16].
The aim of this review is to summarize and critically evaluate state-of-the-art approaches and the most significant outputs related to the development of target-specific radiometal labeled biomolecules for imaging of severe tumor types and tumors with an increased incidence. Recent advances in synthetic approaches and radiometal-labeling strategies of amino acid-based biologically active molecules, including most employed peptide families and receptors such as somatostatin, cholecystokinin/gastrin, bombesin, integrins, and hypoxia endogenous markers, as well as inhibitors of prostate-specific membrane antigen and fibroblast activation protein, are highlighted in order to demonstrate perspectives in cancer diagnostics with amino acid-based radiopharmaceuticals.

Basic Characteristics of Conventional Metal Radionuclides and Chelators Currently Used in Nuclear Medicine
Radiometallic compounds with targeted biodistribution and binding in the human body (i.e., target-specific) include in their structure: (i) biomolecules as a crucial biodistribution component (specific to receptor); (ii) a linker as a connecting component preserving specificity of biomolecule when attaching; (iii) a bifunctional chelating agent (BFCA); and (iv) metal radionuclides (see Figure 1). Basic characteristics of the most important or most frequently used representatives in the group of conventional metal radionuclides and BFCA are briefly discussed in Sections 2.1 and 2.2, respectively. Discussion is led in general point of view or, if appropriate, with respect to amino acid based biomolecules.

Metal Radionuclides
In general, a diagnostic radioprobe contains a gamma emitting radionuclide for SPECT imaging or a positron emitting radionuclide for PET imaging. Basic parameters of the most common metallic radionuclides for diagnostic nuclear medicine are summarized in Table 1.
Nuclear medicine research is currently focused on development of a highly potent target-specific biomolecule labeled with positron emitters (predominantly gallium-68, but also zirconium-89, copper-64, and others). Anyway, there is still a leading position of technetium-99m in diagnostic clinical practice. In research, a prognosis for the development of Tc-radiopharmaceuticals is also quite positive due to novel modifications of BFCA and linkers continuously presented and developed for SPECT imaging.  111 In SPECT of somatostatin receptor-positive NET 67 Ga 93.3 (37%), 184.6 (20.4%), 300.2 (16.6%) 3.26 d cyclotron, 68 Zn(p, 2n) 67 Ga scintigraphy of inflammation, infection, tumors 64 Cu β + 653 (17.6%) 12.7 h cyclotron, 64 Ni(p, n) 64 Cu PET imaging of hypoxic tumors, integrin-and gastrin-releasing peptide receptor-positive tumors 68 Ga 836 (89%) 67.7 m 68 Ge/ 68 Ga generator (cyclotron alternatively) PET imaging of somatostatin receptor-, PSMA-, FAP-overexpressed tumors 89 Zr 395 (23%) 3.3 d cyclotron, 89 Y(p, n) 89 Zr immuno-PET imaging Dosimetry and imaging aspects, depending on a particular radiolabeled compound and its properties, as well as an overall condition of a patient, can be found (if they were evaluated) in individual imaging studies discussed in Section 4.

Bifunctional Chelating Agents (BFCA)
Since the metallic radionuclides themselves cannot be utilized in a direct radiolabeling of amino acid-based target-specific compounds (peptides, proteins), it is necessary to develop bifunctional chelating agents (BFCA) [12]. An appropriate BFCA can properly attach both a metallic radionuclide and a biomolecule as well. The double function of BFCA helps the biomolecule to retain its receptor specificity and, thus, to match metal properties with the intended utilization in the imaging/therapy of various diseases. The choice of BFCA takes into account the oxidation state and nature of the metallic radionuclide. The optimal BFCA should provide thermodynamically stable and kinetically inert complexes, rapid reaction (at low temperatures and concentration), flexible conjugation chemistry, and should be easily accessible [17,18].
Various acyclic and cyclic BFCA have been introduced into (potential) radiopharmaceuticals. Traditional examples of acyclic and cyclic BFCA are discussed in Sections 2.2.1 and 2.2.2, respectively, while the most commonly used BFCA in radiolabeling with a particular diagnostic radiometal including newer developed chelators in Sections 3.2.1-3.2.5.

Acyclic BFCA
The polyaminopolycarboxylic acids-derived BFCA, such as DTPA, EDDA, EDTA, as well as tripeptide MAG3 (Figure 2), are the most commonly used acyclic BFCA containing hard donor atoms (N, O) in their molecule to form the coordination bond with metallic radionuclide. Another acyclic chelator, a siderophore-based desferrioxamine-B (DFO) has been utilized for effective radiolabeling of biomolecules with a metal. The thermodynamic stability and inert kinetics of a formed complex is unique and influenced by properties of both, a metal radionuclide as well as a BFCA. A significant advantage of the acyclic BFCA is faster metal binding kinetics, resulting in a faster radiolabeling procedure [17]. On the contrary, acyclic BFCA form less stable complexes than cyclic ones due to a higher interaction probability and more fixed geometry of donor atoms in the cyclic BFCA [18]. (DFO) has been utilized for effective radiolabeling of biomolecules with a metal. The thermodynamic stability and inert kinetics of a formed complex is unique and influenced by properties of both, a metal radionuclide as well as a BFCA. A significant advantage of the acyclic BFCA is faster metal binding kinetics, resulting in a faster radiolabeling procedure [17]. On the contrary, acyclic BFCA form less stable complexes than cyclic ones due to a higher interaction probability and more fixed geometry of donor atoms in the cyclic BFCA [18].

Cyclic BFCA
The cyclic BFCA containing macrocycle such as DOTA, NOTA, TETA, and their derivatives as well as various structurally related analogues (for selected representatives see Figure 3) are holding an important position in syntheses of radiolabeled peptide-based compounds over a long period. Several new next generation cyclic chelators or chelators derived from traditional ones with improved properties have been developed over past decade such as PCTA, AAZTA, TRAP, THP, and fusarinine C [19]. As mentioned above, cyclic BFCA are beneficial generally by providing more kinetically inert and thermodynamically stable complexes with metal radionuclides. In order to obtain complexes with enhanced stability, several properties have to be considered such as hard and soft acid and base concept, a higher number of donor atoms providing a better steric fixation of complex, and a proper cavity size for the encapsulation of the whole size of metal ion in a tight structural arrangement.

Cyclic BFCA
The cyclic BFCA containing macrocycle such as DOTA, NOTA, TETA, and their derivatives as well as various structurally related analogues (for selected representatives see Figure 3) are holding an important position in syntheses of radiolabeled peptide-based compounds over a long period. Several new next generation cyclic chelators or chelators derived from traditional ones with improved properties have been developed over past decade such as PCTA, AAZTA, TRAP, THP, and fusarinine C [19]. As mentioned above, cyclic BFCA are beneficial generally by providing more kinetically inert and thermodynamically stable complexes with metal radionuclides. In order to obtain complexes with enhanced stability, several properties have to be considered such as hard and soft acid and base concept, a higher number of donor atoms providing a better steric fixation of complex, and a proper cavity size for the encapsulation of the whole size of metal ion in a tight structural arrangement. been increasingly studied to improve kinetic inertness and stability of complexes, especially those with copper isotopes.

Complexes and Radiolabeling Approaches for Target-Specific Peptide Molecules
The amino acids, main peptide and protein building blocks, play an important role essentially in all biological processes. Radiolabeled amino acids (AA) have become actively studied, owing to the role of their transporters in the tumor environment. Studies indicated that AA transporters, which recognize, bind and carry amino acids across the plasma membrane, serve not only to maintain nutritional requirements, but also to accumulate particular amino acids in specific cells [29,30]. DOTA is considered as the golden standard of chelators owing to its high kinetic stability. Several types of DOTA-derived chelators have been developed to bind with target peptide biomolecules, i.e., protected DOTA forms, active DOTA esters, and DOTA-deriva- tives with a coupling moiety [20]. Concerning NOTA, derivatives with aminocarboxylic acids have been applied as BFCA, e.g., NODAGA (with glutaric acid), NODASA (with succinic acid), or NODAPA (with p-phenylacetic acid) [21]. Abrams and co-workers used 6-hydrazinopyridin-3-carboxylic acid, in short HYNIC, for radiolabeling of a polyclonal antibody with technetium-99m [22]. Ever since, HYNIC has become the most convenient chelator for 99m Tc-labeled peptides and antibodies. Other chelators related to bisthiosemicarbazone [23,24], cyclam [25,26], and sarcophagine [27,28] have been increasingly studied to improve kinetic inertness and stability of complexes, especially those with copper isotopes.

Complexes and Radiolabeling Approaches for Target-Specific Peptide Molecules
The amino acids, main peptide and protein building blocks, play an important role essentially in all biological processes. Radiolabeled amino acids (AA) have become actively studied, owing to the role of their transporters in the tumor environment. Studies indicated that AA transporters, which recognize, bind and carry amino acids across the plasma membrane, serve not only to maintain nutritional requirements, but also to accumulate particular amino acids in specific cells [29,30].
Analogically, radiolabeled peptides as amino acid-based biomolecules are in the center of interest in the field of nuclear medicine and pharmacy because their biological action is mediated upon selective binding to specific peptide receptors and transporters overexpressed in numerous tumor cells. These receptors have shown potential as a molecular target for tumor imaging or targeted therapy with radiolabeled peptides (for the most important onco-specific peptide receptors and radiolabeled peptides see Section 4). The following Sections 3.2-3.4 are dealing with current radiolabeling approaches used for peptides and showing corresponding complex structures.

Peptides as Target-Specific Molecules and Their Synthesis
Peptides can be simply synthesized by a solid phase peptide synthesis (SPPS) [31,32] and modified to obtain optimized pharmacokinetic properties. The synthetic procedure can be carried out manually [33], e.g., in syringes, or automatically in commercial synthesizers [34]. A general pattern for the solid-phase peptide synthesis is depicted in Figure 4.  The advantages of peptides over proteins and antibodies can be seen in a preparation method, a rapid blood clearance, and the ability to tolerate harsh reaction conditions. On the other hand, a rapid enzymatic degradation by physiological peptidases is a significant limitation of peptides. Anyway, there are several strategies how to avoid this drawback including structural modifications of the C-/N-terminus, incorporation of a The advantages of peptides over proteins and antibodies can be seen in a preparation method, a rapid blood clearance, and the ability to tolerate harsh reaction conditions. On the other hand, a rapid enzymatic degradation by physiological peptidases is a significant limitation of peptides. Anyway, there are several strategies how to avoid this drawback including structural modifications of the C-/N-terminus, incorporation of a PEG linker or D-/unnatural AA, and cyclization [35].

Conventional Radiolabeling Approaches of Peptides with Metallic Radionuclide
The choice of a radiolabeling approach depends on radionuclide nature and a bioactive molecule. A direct labeling strategy is more difficult to be used for a metal attachment to biomolecules (e.g., peptides, proteins). Since the direct approach provides low site-specific and unstable products, and is applicable only to antibodies and their fragments, an indirect labeling method with BFCA has become preferred for a metal-peptide linkage. The usage of BFCA often requires multistep synthesis and involves non-specific interactions, thus a searching for new strategies with more effective incorporation of BFCA into peptide biomolecules has led to innovative approaches in the radiochemistry field such as click reactions (Section 3.3) and radiolabeled nanoparticles (Section 3.4). Modified BFCA and linkers may improve pharmacokinetic properties of a radiolabeled compound. Conventional radiolabeling approaches and chemical structures of corresponding complexes with the most frequently used metal diagnostic radionuclides are discussed in following Sections 3.2.1-3.2.5.

Radiolabeling of Peptide-Based Compounds with Technetium-99m
Technetium-99m has been the most frequently used radionuclide in nuclear medicine since the 99 Mo/ 99m Tc generator development in 1957. Indirect labeling approaches, such as pre-labeling (labeling before conjugation with biomolecule) or post-labeling (labeling after conjugation with biomolecule), are of the routine for 99m Tc-coordination. The pre-labeling procedure ( Figure 5) is very useful in research to prove the concept and define the chemistry, contrary to a clinical use because of a long lasting radiosynthesis and hardly accomplished kit formulation [3]. . Scheme of the pre-labeling procedure with technetium-99m (adapted according to [3]).
The post-labeling procedure ( Figure 6) is the most widely used for a synthesis of target-specific peptide radiopharmaceuticals. Figure 6. Scheme of the post-labeling procedure with technetium-99m (adapted according to [3]).
Technetium chemistry, its cores and complexes, have been thoroughly reviewed in recent years [4,6,36,37]. The most frequently studied BFCA for Tc-complexes are summarized in Table 2. In past few years, [ 99m Tc]Tc-HYNIC has been the most commonly used core for the conventional radiolabeling of bioactive peptides for tumor imaging such as RGD peptides [38,39], α-MSH peptide analogues [40,41], bombesin analogues [42,43], substance P analogues [44], or glucagon-like peptide analogues [45].  The post-labeling procedure ( Figure 6) is the most widely used for a synthesis of target-specific peptide radiopharmaceuticals.  Figure 5. Scheme of the pre-labeling procedure with technetium-99m (adapted according to [3]).
The post-labeling procedure ( Figure 6) is the most widely used for a synthesis of target-specific peptide radiopharmaceuticals. Figure 6. Scheme of the post-labeling procedure with technetium-99m (adapted according to [3]).
Technetium chemistry, its cores and complexes, have been thoroughly reviewed in recent years [4,6,36,37]. The most frequently studied BFCA for Tc-complexes are summarized in Table 2. In past few years, [ 99m Tc]Tc-HYNIC has been the most commonly used core for the conventional radiolabeling of bioactive peptides for tumor imaging such as RGD peptides [38,39], α-MSH peptide analogues [40,41], bombesin analogues [42,43], substance P analogues [44], or glucagon-like peptide analogues [45]. Gallium is represented by the oxidation state III+ in aqueous solution and acts as a hard Lewis acid. It binds to hard Lewis bases such as nitrogen and oxygen donor groups [46] MAG3 Figure 6. Scheme of the post-labeling procedure with technetium-99m (adapted according to [3]).
Technetium chemistry, its cores and complexes, have been thoroughly reviewed in recent years [4,6,36,37]. The most frequently studied BFCA for Tc-complexes are summarized in Table 2. In past few years, [ 99m Tc]Tc-HYNIC has been the most commonly used core for the conventional radiolabeling of bioactive peptides for tumor imaging such as RGD peptides [38,39], α-MSH peptide analogues [40,41], bombesin analogues [42,43], substance P analogues [44], or glucagon-like peptide analogues [45]. Gallium is represented by the oxidation state III+ in aqueous solution and acts as a hard Lewis acid. It binds to hard Lewis bases such as nitrogen and oxygen donor groups [47] HYNIC (with tricine coligand) Figure 6. Scheme of the post-labeling procedure with technetium-99m (adapted according to [3]).
Technetium chemistry, its cores and complexes, have been thoroughly reviewed in recent years [4,6,36,37]. The most frequently studied BFCA for Tc-complexes are summarized in Table 2. In past few years, [ 99m Tc]Tc-HYNIC has been the most commonly used core for the conventional radiolabeling of bioactive peptides for tumor imaging such as RGD peptides [38,39], α-MSH peptide analogues [40,41], bombesin analogues [42,43], substance P analogues [44], or glucagon-like peptide analogues [45]. Gallium is represented by the oxidation state III+ in aqueous solution and acts as a hard Lewis acid. It binds to hard Lewis bases such as nitrogen and oxygen donor groups [48] 3.2.2. Radiolabeling of Peptide-Based Compounds with Gallium-68 Gallium is represented by the oxidation state III+ in aqueous solution and acts as a hard Lewis acid. It binds to hard Lewis bases such as nitrogen and oxygen donor groups of carboxylates, hydroxamates, amines [17]. It can be relatively easy hydrolyzed at pH 4-7 [49]. Gallium forms complexes with the maximum coordination number of 6 in a pseudo octahedral geometry, but four-or five-coordinate complexes are also formed [17,49] For a 68 Ga-labeling procedure, well-known representatives and the most frequently used BFCA are derived from 1,4,7-triazacyclononane and 1,4,7,10-tetraazacyclododecane, e.g., DOTA and NOTA, including their recently developed derivatives such as TRAP, PCTA, NOTP, and THP and DATA, among others (see examples in Table 3). of carboxylates, hydroxamates, amines [17]. It can be relatively easy hydrolyzed at pH 4-7 [49]. Gallium forms complexes with the maximum coordination number of 6 in a pseudo octahedral geometry, but four-or five-coordinate complexes are also formed [17,49] For a 68 Ga-labeling procedure, well-known representatives and the most frequently used BFCA are derived from 1,4,7-triazacyclononane and 1,4,7,10-tetraazacyclododecane, e.g., DOTA and NOTA, including their recently developed derivatives such as TRAP, PCTA, NOTP, and THP and DATA, among others (see examples in Table 3).
THP and its derivatives [57] The 68 Ga-labeled biomolecules have been studied for somatostatin receptor-positive tumor imaging over a long period [58][59][60] with several highly potent agents in clinical trials or one already approved. Current studies with gallium-68 have followed up various malignancies with prostate-specific membrane antigen (PSMA) and fibroblast activation protein (FAP) [55,61,62].

Radiolabeling of Peptide-Based Compounds with Indium-111
Indium-111 has several properties for coordination chemistry with gallium-68 in common. The only stable oxidation state of indium-111 is III+ and acts as the Lewis acid, but softer donor groups can be offered to create seven or eight-coordinated complexes [49]. The ionic radius of indium-111 (0.92 Å) is significantly larger than that of gallium-68 (0.65 Å) what results in different coordination in macrocycles. The DTPA-and DOTA-based chelators usually in t-butyl forms are generally the most employed for the 111 In-labeling (see Table 4) [63].

BFCA
Complex Structure References [57] The 68 Ga-labeled biomolecules have been studied for somatostatin receptor-positive tumor imaging over a long period [58][59][60] with several highly potent agents in clinical trials or one already approved. Current studies with gallium-68 have followed up various malignancies with prostate-specific membrane antigen (PSMA) and fibroblast activation protein (FAP) [55,61,62].

Radiolabeling of Peptide-Based Compounds with Indium-111
Indium-111 has several properties for coordination chemistry with gallium-68 in common. The only stable oxidation state of indium-111 is III+ and acts as the Lewis acid, but softer donor groups can be offered to create seven or eight-coordinated complexes [49]. chelators usually in t-butyl forms are generally the most employed for the 111 In-labeling (see Table 4) [63]. Indium-111 has several properties for coordination chemistry with gallium-68 in common. The only stable oxidation state of indium-111 is III+ and acts as the Lewis acid, but softer donor groups can be offered to create seven or eight-coordinated complexes [49]. The ionic radius of indium-111 (0.92 Å) is significantly larger than that of gallium-68 (0.65 Å) what results in different coordination in macrocycles. The DTPA-and DOTA-based chelators usually in t-butyl forms are generally the most employed for the 111 In-labeling (see Table 4) [63].

Radiolabeling of Peptide-Based Compounds with Copper-64
The most stable oxidation state of copper in aqueous solution is II+ creating complexes with donor atoms such as amine-, imine-and pyridine-N, carboxylate-O, and thiol-S [17]. Although the copper chelation chemistry has been thoroughly reviewed [13,18,49,71], there is still a challenge in the development of in vivo stable Cu-BFCA complexes due to labile character of Cu(II). The design of copper radiopharmaceuticals has put emphasis on polyaza-macrocycles derived BFCA (see Table 5). Due to only moderate stability of [ 64 Cu]Cu-DOTA-labeled biomolecules under in vivo conditions [64,65] DTPA and its derivatives 3.2.3. Radiolabeling of Peptide-Based Compounds with Indium-111 Indium-111 has several properties for coordination chemistry with gallium-68 in common. The only stable oxidation state of indium-111 is III+ and acts as the Lewis acid, but softer donor groups can be offered to create seven or eight-coordinated complexes [49]. The ionic radius of indium-111 (0.92 Å) is significantly larger than that of gallium-68 (0.65 Å) what results in different coordination in macrocycles. The DTPA-and DOTA-based chelators usually in t-butyl forms are generally the most employed for the 111 In-labeling (see Table 4) [63].

Radiolabeling of Peptide-Based Compounds with Copper-64
The most stable oxidation state of copper in aqueous solution is II+ creating complexes with donor atoms such as amine-, imine-and pyridine-N, carboxylate-O, and thiol-S [17]. Although the copper chelation chemistry has been thoroughly reviewed [13,18,49,71], there is still a challenge in the development of in vivo stable Cu-BFCA complexes due to labile character of Cu(II). The design of copper radiopharmaceuticals has put emphasis on polyaza-macrocycles derived BFCA (see Table 5). Due to only moderate stability of [ 64 Cu]Cu-DOTA-labeled biomolecules under in vivo conditions [66] Studies covering 111 In-labeled biomolecules are aimed at somatostatin receptor imaging [66], glucagon-like peptide receptor [67,68], gastrin-releasing peptide receptor [69], or integrins [70].

Radiolabeling of Peptide-Based Compounds with Copper-64
The most stable oxidation state of copper in aqueous solution is II+ creating complexes with donor atoms such as amine-, imine-and pyridine-N, carboxylate-O, and thiol-S [17]. Although the copper chelation chemistry has been thoroughly reviewed [13,18,49,71], there is still a challenge in the development of in vivo stable Cu-BFCA complexes due to labile character of Cu(II). The design of copper radiopharmaceuticals has put emphasis on polyaza-macrocycles derived BFCA (see Table 5). Due to only moderate stability of [ 64 Cu]Cu-DOTA-labeled biomolecules under in vivo conditions and high liver accumulation, a number of cross-bridged cyclam derivatives were developed to form more stable 64 Cu-complexes [25,26,72]. 64 Cu-labeled compounds have been included, mostly in the studies of tumors with overexpressed gastrin-releasing peptide [73,74] and α ν β 3 integrin receptors [75,76], and prostate-specific membrane antigen [77]. and high liver accumulation, a number of cross-bridged cyclam derivatives were developed to form more stable 64 Cu-complexes [25,26,72]. 64 Cu-labeled compounds have been included, mostly in the studies of tumors with overexpressed gastrin-releasing peptide [73,74] and ανβ3 integrin receptors [75,76], and prostate-specific membrane antigen [77].

Radiolabeling of Peptide-Based Compounds with Zirconium-89
Zirconium is a metal belonging to the group IV that exists primarily in +IV oxidation state in aqueous media. This cation is relatively large, acts as the hard Lewis acid and prefers anionic oxygen donor groups to create complexes with high coordination number [86]. Depending on pH, oxides and hydroxides of zirconium form polynuclear species upon hydrolysis at very low pH and mononuclear hydrolysis species at pH between 0 and 2 [87].
Zirconium-89 has been applied mostly in labeling of monoclonal antibodies for PET imaging of immune-based strategies [88], but there has been a progress in the design of 89 Zr-labeled small peptide PSMA-inhibitors for prostate cancer imaging lately [89]. Table 6. The most common BFCA for 89 Zr-labeled compounds.

DFO and its derivatives
In order to effectively utilize zirconium-89, various chelators have been employed such as DOTA, DTPA, as well as the most successful desferrioxamine B and 3-hydroxypyridin-2-one (2,3-HOPO) derivatives (see Table 6).
Zirconium-89 has been applied mostly in labeling of monoclonal antibodies for PET imaging of immune-based strategies [88], but there has been a progress in the design of 89 Zr-labeled small peptide PSMA-inhibitors for prostate cancer imaging lately [89].

Radiolabeling Approaches of Peptides with Metallic Radionuclide Based on Click-Chemistry
Since Kolb et al. described "click reactions" in 2001 [92], this new chemistry has become rapidly growing in various chemical fields and, since 2006, also in the radiochemistry field. There are two main characteristics making the click chemistry attractive, i.e., the bioorthogonality of reactions and mild reaction conditions (usually at room temperature and in aqueous media) [93]. Additional benefits include the selectivity, rapidity, and modularity of click ligations. The most associated term with the "click chemistry" is the Cu(I)-catalyzed azide-alkyne cycloaddition (CuAAC) forming 1,4-disubstituted 1,2,3-triazoles (see Figure 7A). Mindt et al. developed and extended the "click-to-chelate" methodology for radiometallic ligation [94,95], in which 1,2,3-triazole is an integral part of the chelating system. This approach has been successfully applied for Tc-and Re-tricarbonyl compounds, when tridentate ligands are coordinated to M(CO)3 core resulting in better pharmacokinetic properties [94,95].
In recent years, several catalyst-free site-specific reactions have been investigated for effective radiolabeling of peptide biomolecules and nanomaterials including te- [89] 2,3-HOPO and its derivatives In order to effectively utilize zirconium-89, various chelators have been employed such as DOTA, DTPA, as well as the most successful desferrioxamine B and 3-hydroxypyridin-2-one (2,3-HOPO) derivatives (see Table 6).
Zirconium-89 has been applied mostly in labeling of monoclonal antibodies for PET imaging of immune-based strategies [88], but there has been a progress in the design of 89 Zr-labeled small peptide PSMA-inhibitors for prostate cancer imaging lately [89].

Radiolabeling Approaches of Peptides with Metallic Radionuclide Based on Click-Chemistry
Since Kolb et al. described "click reactions" in 2001 [92], this new chemistry has become rapidly growing in various chemical fields and, since 2006, also in the radiochemistry field. There are two main characteristics making the click chemistry attractive, i.e., the bioorthogonality of reactions and mild reaction conditions (usually at room temperature and in aqueous media) [93]. Additional benefits include the selectivity, rapidity, and modularity of click ligations. The most associated term with the "click chemistry" is the Cu(I)-catalyzed azide-alkyne cycloaddition (CuAAC) forming 1,4-disubstituted 1,2,3-triazoles (see Figure 7A). Mindt et al. developed and extended the "click-to-chelate" methodology for radiometallic ligation [94,95], in which 1,2,3-triazole is an integral part of the chelating system. This approach has been successfully applied for Tc-and Re-tricarbonyl compounds, when tridentate ligands are coordinated to M(CO)3 core resulting in better pharmacokinetic properties [94,95].
In recent years, several catalyst-free site-specific reactions have been investigated for effective radiolabeling of peptide biomolecules and nanomaterials including te- [90] DTPA and its derivatives such as DOTA, DTPA, as well as the most successful desferrioxamine B and 3-hydroxypyridin-2-one (2,3-HOPO) derivatives (see Table 6).
Zirconium-89 has been applied mostly in labeling of monoclonal antibodies for PET imaging of immune-based strategies [88], but there has been a progress in the design of 89 Zr-labeled small peptide PSMA-inhibitors for prostate cancer imaging lately [89].

Radiolabeling Approaches of Peptides with Metallic Radionuclide Based on Click-Chemistry
Since Kolb et al. described "click reactions" in 2001 [92], this new chemistry has become rapidly growing in various chemical fields and, since 2006, also in the radiochemistry field. There are two main characteristics making the click chemistry attractive, i.e., the bioorthogonality of reactions and mild reaction conditions (usually at room temperature and in aqueous media) [93]. Additional benefits include the selectivity, rapidity, and modularity of click ligations. The most associated term with the "click chemistry" is the Cu(I)-catalyzed azide-alkyne cycloaddition (CuAAC) forming 1,4-disubstituted 1,2,3-triazoles (see Figure 7A). Mindt et al. developed and extended the "click-to-chelate" methodology for radiometallic ligation [94,95], in which 1,2,3-triazole is an integral part of the chelating system. This approach has been successfully applied for Tc-and Re-tricarbonyl compounds, when tridentate ligands are coordinated to M(CO)3 core resulting in better pharmacokinetic properties [94,95].
In recent years, several catalyst-free site-specific reactions have been investigated for effective radiolabeling of peptide biomolecules and nanomaterials including te- [91] 3.3. Radiolabeling Approaches of Peptides with Metallic Radionuclide Based on Click-Chemistry Since Kolb et al. described "click reactions" in 2001 [92], this new chemistry has become rapidly growing in various chemical fields and, since 2006, also in the radiochemistry field. There are two main characteristics making the click chemistry attractive, i.e., the bioorthogonality of reactions and mild reaction conditions (usually at room temperature and in aqueous media) [93]. Additional benefits include the selectivity, rapidity, and modularity of click ligations. The most associated term with the "click chemistry" is the Cu(I)catalyzed azide-alkyne cycloaddition (CuAAC) forming 1,4-disubstituted 1,2,3-triazoles (see Figure 7A). Mindt et al. developed and extended the "click-to-chelate" methodology for radiometallic ligation [94,95], in which 1,2,3-triazole is an integral part of the chelating system. This approach has been successfully applied for Tc-and Re-tricarbonyl compounds, when tridentate ligands are coordinated to M(CO) 3 core resulting in better pharmacokinetic properties [94,95].

Radiolabeling Approaches of Peptides with Metallic Radionuclide Based on Nanoparticles
Nanomedicine has recently emerged as one of the most promising branches in medicine including a development of novel probes with improved properties for the site-specific detection or therapy of cancer. This rapidly growing trend is underlined by numerous reviews in the radiochemistry field [114][115][116][117]. Over past 10 years, tens of articles have been focused on the metal-labeled nanoparticles (NP) conjugated to various peptides for SPECT and PET cancer imaging (see a representative image of radiolabeled nanoparticles using electron microscopy in Figure 9). Radiolabeling of NPs with technetium-99m can be carried out by a direct or an indirect method. The direct approach is based on a reduction in [ 99m Tc]TcO4 − with the acidic solution of stannous chloride followed by its direct binding and incorporation to a NP core. In the indirect method, BFCA is necessary to allow a stable linkage between radionuclide and NP [116]. The indirect method has been mostly used for the radiolabeling of 99m Tc-NPs conjugated with peptides, see an illustrative example in Figure 10. Gold NPs have been conjugated to peptides with [ 99m Tc]Tc-HYNIC for integrin-positive glio-

Radiolabeling Approaches of Peptides with Metallic Radionuclide Based on Nanoparticles
Nanomedicine has recently emerged as one of the most promising branches in medicine including a development of novel probes with improved properties for the site-specific detection or therapy of cancer. This rapidly growing trend is underlined by numerous reviews in the radiochemistry field [114][115][116][117]. Over past 10 years, tens of articles have been focused on the metal-labeled nanoparticles (NP) conjugated to various peptides for SPECT and PET cancer imaging (see a representative image of radiolabeled nanoparticles using electron microscopy in Figure 9).

Radiolabeling Approaches of Peptides with Metallic Radionuclide Based on Nanoparticles
Nanomedicine has recently emerged as one of the most promising branches in medicine including a development of novel probes with improved properties for the site-specific detection or therapy of cancer. This rapidly growing trend is underlined by numerous reviews in the radiochemistry field [114][115][116][117]. Over past 10 years, tens of articles have been focused on the metal-labeled nanoparticles (NP) conjugated to various peptides for SPECT and PET cancer imaging (see a representative image of radiolabeled nanoparticles using electron microscopy in Figure 9). Radiolabeling of NPs with technetium-99m can be carried out by a direct or an indirect method. The direct approach is based on a reduction in [ 99m Tc]TcO4 − with the acidic solution of stannous chloride followed by its direct binding and incorporation to a NP core. In the indirect method, BFCA is necessary to allow a stable linkage between radionuclide and NP [116]. The indirect method has been mostly used for the radiolabeling of 99m Tc-NPs conjugated with peptides, see an illustrative example in Figure 10. Gold NPs have been conjugated to peptides with [ 99m Tc]Tc-HYNIC for integrin-positive glio- Radiolabeling of NPs with technetium-99m can be carried out by a direct or an indirect method. The direct approach is based on a reduction in [ 99m Tc]TcO 4 − with the acidic solution of stannous chloride followed by its direct binding and incorporation to a NP core. In the indirect method, BFCA is necessary to allow a stable linkage between radionuclide and NP [116]. The indirect method has been mostly used for the radiolabeling of 99m Tc-NPs conjugated with peptides, see an illustrative example in Figure 10. Gold NPs have been conjugated to peptides with [ 99m Tc]Tc-HYNIC for integrin-positive glioma imaging [119], with [ 99m Tc]Tc-DTPA for breast cancer imaging [120], for gastrin releasing peptide receptor imaging [121,122] and somatostatin receptor-positive neuroendocrine tumor imaging [123]. The NPs based on a polylactic acid polymer were conjugated to 99m Tc-labeled octreotide for pancreatic polypeptide-secreting tumor imaging [124].  [120], for gastrin releasing peptide receptor imaging [121,122] and somatostatin receptor-positive neuroendocrine tumor imaging [123]. The NPs based on a polylactic acid polymer were conjugated to 99m Tc-labeled octreotide for pancreatic polypeptide-secreting tumor imaging [124]. Several published papers dealt with 111 In-labeled NPs conjugated to peptides such as directly labeled gold NPs for human melanoma and glioblastoma imaging [125], liposomal NPs conjugated to a RGD peptide analogue and the undecapeptide substance P for glioblastoma and melanoma targeting [126].

Onco-Receptors and Their Target-Specific Radiometal Labeled Peptide Molecules for Tumor Imaging
In the following Sections 4.1-4.6, the most commonly studied onco-receptors are summarized, briefly characterized (location and purpose in human body), and discussed in relation to the development and improvements in their significant radiometal labeled ligands and tumor imaging. In a similar way, radiometal labeled peptide inhibitors of tumor-related proteins (Section 4.7) and sulfonamide-based analogues for tumor hypoxia imaging (Section 4.8) are discussed. In the accompanied tables, examples of particular radiolabeled analogues along with corresponding onco-receptors used in a positive tumor imaging over past three years, advantages and limitations of the studied diagnostic systems are critically evaluated. An illustrative example of a study of radiolabeled [ 68 Ga]Ga-OPS202 and [ 68 Ga]Ga-DOTATOC biomolecules for NET imaging is in Figure  11. Several published papers dealt with 111 In-labeled NPs conjugated to peptides such as directly labeled gold NPs for human melanoma and glioblastoma imaging [125], liposomal NPs conjugated to a RGD peptide analogue and the undecapeptide substance P for glioblastoma and melanoma targeting [126].

Onco-Receptors and Their Target-Specific Radiometal Labeled Peptide Molecules for Tumor Imaging
In the following Sections 4.1-4.6, the most commonly studied onco-receptors are summarized, briefly characterized (location and purpose in human body), and discussed in relation to the development and improvements in their significant radiometal labeled ligands and tumor imaging. In a similar way, radiometal labeled peptide inhibitors of tumor-related proteins (Section 4.7) and sulfonamide-based analogues for tumor hypoxia imaging (Section 4.8) are discussed. In the accompanied tables, examples of particular radiolabeled analogues along with corresponding onco-receptors used in a positive tumor imaging over past three years, advantages and limitations of the studied diagnostic systems are critically evaluated. An illustrative example of a study of radiolabeled [ 68 Ga]Ga-OPS202 and [ 68 Ga]Ga-DOTATOC biomolecules for NET imaging is in Figure 11.

Somatostatin and Its Analogues for Somatostatin Receptors (SSTR) Imaging
Somatostatin (SST) is a physiological hormone occurring in two biologically active forms with the AA sequences illustrated in Figure 12. It regulates an endocrine and exocrine secretion throughout a human body. The biological effects of SST are mediated via 5 types of somatostatin receptors (SSTR) belonging to a G-protein coupled receptors family. SST, its analogues and receptors, have become increasingly popular and widely studied because of anti-tumor effects and mechanisms, including GEP-NETs [132], pituitary adenomas [133], breast cancer [134], small-cell lung cancer [135], melanoma [136], etc. The most commonly expressed receptor subtype in tumor cells is SSTR2, followed by SSTR1, SSTR5, SSTR3, and SSTR4 as the least expressed subtype [137]. Due to short biological half-lives of the natural SST, various synthetic analogues have been designed and evaluated to obtain more stable compounds (see Table 7). It can be stated, based on the examined published papers, there is a great effort to modify the DOTA-octreotide structure in order to achieve novel SST analogues with even better pharmacokinetic properties and specificity to avoid an intense uptake in liver, spleen, and kidney. The SST analogues labeled with gallium-68 and DOTA currently represent the best procedure for GEP-NET imaging. This statement is supported with a large number of research articles that include [ 68 Ga]Ga-DOTANOC, DOTATATE, and DOTATOC, respectively, for imaging of various tumors, such as head and neck paraganglioma [138]; pituitary adenoma and meningioma [139]; thyroid [140] and lung [141] carcinoma; and tumors in gastrointestinal system [60] as well. According to available literature from 2010, new approaches for syntheses of the SSTR-ligands seem to be not so extent, but since then, many consecutive examinations and reports

Somatostatin and Its Analogues for Somatostatin Receptors (SSTR) Imaging
Somatostatin (SST) is a physiological hormone occurring in two biologically active forms with the AA sequences illustrated in Figure 12. It regulates an endocrine and exocrine secretion throughout a human body.

Somatostatin and Its Analogues for Somatostatin Receptors (SSTR) Imaging
Somatostatin (SST) is a physiological hormone occurring in two biologically active forms with the AA sequences illustrated in Figure 12. It regulates an endocrine and exocrine secretion throughout a human body. The biological effects of SST are mediated via 5 types of somatostatin receptors (SSTR) belonging to a G-protein coupled receptors family. SST, its analogues and receptors, have become increasingly popular and widely studied because of anti-tumor effects and mechanisms, including GEP-NETs [132], pituitary adenomas [133], breast cancer [134], small-cell lung cancer [135], melanoma [136], etc. The most commonly expressed receptor subtype in tumor cells is SSTR2, followed by SSTR1, SSTR5, SSTR3, and SSTR4 as the least expressed subtype [137]. Due to short biological half-lives of the natural SST, various synthetic analogues have been designed and evaluated to obtain more stable compounds (see Table 7). It can be stated, based on the examined published papers, there is a great effort to modify the DOTA-octreotide structure in order to achieve novel SST analogues with even better pharmacokinetic properties and specificity to avoid an intense uptake in liver, spleen, and kidney. The SST analogues labeled with gallium-68 and DOTA currently represent the best procedure for GEP-NET imaging. This statement is supported with a large number of research articles that include [ 68 Ga]Ga-DOTANOC, DOTATATE, and DOTATOC, respectively, for imaging of various tumors, such as head and neck paraganglioma [138]; pituitary adenoma and meningioma [139]; thyroid [140] and lung [141] carcinoma; and tumors in gastrointestinal system [60] as well. According to available literature from 2010, new approaches for syntheses of the SSTR-ligands seem to be not so extent, but since then, many consecutive examinations and reports The biological effects of SST are mediated via 5 types of somatostatin receptors (SSTR) belonging to a G-protein coupled receptors family. SST, its analogues and receptors, have become increasingly popular and widely studied because of anti-tumor effects and mechanisms, including GEP-NETs [132], pituitary adenomas [133], breast cancer [134], small-cell lung cancer [135], melanoma [136], etc. The most commonly expressed receptor subtype in tumor cells is SSTR2, followed by SSTR1, SSTR5, SSTR3, and SSTR4 as the least expressed subtype [137]. Due to short biological half-lives of the natural SST, various synthetic analogues have been designed and evaluated to obtain more stable compounds (see Table 7). It can be stated, based on the examined published papers, there is a great effort to modify the DOTA-octreotide structure in order to achieve novel SST analogues with even better pharmacokinetic properties and specificity to avoid an intense uptake in liver, spleen, and kidney. The SST analogues labeled with gallium-68 and DOTA currently represent the best procedure for GEP-NET imaging. This statement is supported with a large number of research articles that include [ 68 Ga]Ga-DOTANOC, DOTATATE, and DOTATOC, respectively, for imaging of various tumors, such as head and neck paraganglioma [138]; pituitary adenoma and meningioma [139]; thyroid [140] and lung [141] carcinoma; and tumors in gastrointestinal system [60] as well. According to available literature from 2010, new approaches for syntheses of the SSTR-ligands seem to be not so extent, but since then, many consecutive examinations and reports have already been comprised of proven ligands for a variety of GEP-NET imaging in clinical trials. Table 7. Summary of radiolabeled somatostatin analogues for SSTR-positive tumor imaging over past 3 years.

Bombesin and Its Analogues for Gastrin-Releasing Peptide Receptor (GRPR) Imaging
Bombesin (BBN) is a 14 AA peptide analogue (see the sequence in Figure 13) to the gastrin-releasing peptide and it represents an interesting probe for targeting of gastrinreleasing peptide receptors (GRPR) relevant in oncology.

Bombesin and Its Analogues for Gastrin-Releasing Peptide Receptor (GRPR) Imaging
Bombesin (BBN) is a 14 AA peptide analogue (see the sequence in Figure 13) to the gastrin-releasing peptide and it represents an interesting probe for targeting of gastrin-releasing peptide receptors (GRPR) relevant in oncology. In total, four receptors belong to the family of GRPR, namely neuromendin B receptor BBR1, gastrin-releasing peptide receptor BBR2, orphan receptor BBR3, and amphibious receptor BBR4. Predominantly the BBR2 is upregulated in cancer cells such as breast, lung, pancreas, colon, and prostate [149]. Research with radiolabeled BBN analogues has become increasing since the development of [ 99m Tc]Tc-Lys 3 -BBN in 1998 [150]. Since then, most of these radiolabeled analogues have been designed as GRPR agonists with a favorable internalization in cancer cells. Meanwhile, several studies have demonstrated unwanted side effects of agonists connected with their GRPR activation, thus a research field has shifted its interest to antagonists [151]. Radiolabeled GRPR antagonists have shown superior value to the agonists in terms of better pharmacokinetic properties, very good in vivo stability and, by that, sufficient retention in cancer cells [152]. New GRPR antagonists have been developed with a potential for the clinical translations (see summarized studies in Table 8). Table 8. Summary of radiolabeled bombesin analogues for GRPR-positive tumor imaging over past 3 years.

Results and Findings -Phase of Trials -Cancer Type Studied -Imaging Technique Used -Benefits/Limitations/Conclusion
Reference -67 Ga, 68 Ga, 111 In, 177 Lu -DOTA -p-aminomethylaniline-diglycolic acid -NeoBOMB1 -preclinical in vitro, in vivo; clinical, 4 patients -prostate -PET/CT -[ 68 Ga]Ga-NeoBOMB1 with preserved GRPR affinity, high in vivo stability, and high contrast image in patients [152] - 55 Co, 57 Co -NOTA -PEG2 -RM26 -preclinical in vitro, in vivo -prostate -SPECT/CT, PET/CT -favorable pharmacokinetics and 3-fold lower internalization of 55 Co-labeled peptide compared to 111 In-labeled conjugate making it potential "next day" high contrast PET imaging probe  In total, four receptors belong to the family of GRPR, namely neuromendin B receptor BBR 1 , gastrin-releasing peptide receptor BBR 2 , orphan receptor BBR 3 , and amphibious receptor BBR 4 . Predominantly the BBR 2 is upregulated in cancer cells such as breast, lung, pancreas, colon, and prostate [149]. Research with radiolabeled BBN analogues has become increasing since the development of [ 99m Tc]Tc-Lys 3 -BBN in 1998 [150]. Since then, most of these radiolabeled analogues have been designed as GRPR agonists with a favorable internalization in cancer cells. Meanwhile, several studies have demonstrated unwanted side effects of agonists connected with their GRPR activation, thus a research field has shifted its interest to antagonists [151]. Radiolabeled GRPR antagonists have shown superior value to the agonists in terms of better pharmacokinetic properties, very good in vivo stability and, by that, sufficient retention in cancer cells [152]. New GRPR antagonists have been developed with a potential for the clinical translations (see summarized studies in Table 8). Table 8. Summary of radiolabeled bombesin analogues for GRPR-positive tumor imaging over past 3 years.

Cholecystokinin and Its Analogues for Cholecystokinin Receptor (CCKR) Imaging
Cholecystokinin (CCK) is a peptide hormone, which regulates various actions predominantly in the gastrointestinal tract and central nervous system. CCK was initially characterized with a 33 AA sequence, but later, the peptide was shown to be present in more biologically active forms (e.g., CCK4, CCK8, CCK33, CCK39) derived from a 115 AA precursor [159]. A total of three types of CCK receptors from the G-protein coupled receptors family have been identified, CCK1 known as CCK A, CCK2 known as CCK B, and CCK2i4sv receptor, respectively. The extensively studied receptors are CCK1, characterized in pancreatic cells and mainly located in periphery, and CCK2 located in the brain, stomach, pancreas, and gall bladder, and overexpressed in cancer types such as small cell lung cancers and medullary thyroid carcinomas [159]. The cholecystokinin octapeptide CCK8 (see its AA sequence in Figure 14) and minigastrin are of the most evaluated molecules for CCK2 receptors. All synthesized peptide analogues have the C-terminal receptor-binding tetrapeptide sequence of Trp-Met-Asp-Phe-NH 2 in common. Many of the CCK8 and minigastrin analogues were developed and evaluated up to 2010, the studies over past 3 years are summarized in Table 9. evaluated molecules for CCK2 receptors. All synthesized peptide analo C-terminal receptor-binding tetrapeptide sequence of Trp-Met-Asp-Phe mon. Many of the CCK8 and minigastrin analogues were developed and e 2010, the studies over past 3 years are summarized in Table 9. Glucagon-like peptide 1 (GLP-1) is an intestinal peptide hormone wi quence (see Figure 15), which stimulates insulin secretion. An action of the  Table 9. Summary of radiolabeled CCK/minigastrin analogues for CCKR-positive tumor imaging over past 3 years.

Results and Findings -Phase of Trials -Cancer Type Studied -Imaging Technique Used -Benefits/Limitations/Conclusion
Reference -68 Ga, 89 Zr -fusarinine C (FSC) -x -MG11 -preclinical in vitro, in vivo -epidermoid -microPET/CT -decreased hydrophilicity, increased metabolic stability and kidney retention for dimer and trimer, and reduced TBR of 89 Zr-monomer and dimers

Exendin Analogues for Glucagon-Like Peptide 1 (GLP-1) Receptor Imaging
Glucagon-like peptide 1 (GLP-1) is an intestinal peptide hormone with a 36 AA sequence (see Figure 15), which stimulates insulin secretion. An action of the GLP-1 and its analogues is mediated through a glucagon-like peptide-1 receptor as a class B of G-protein-coupled receptor. The GLP-1 receptor was identified by radioligand binding experiments [164] and is expressed mainly in the stomach, pancreas, and brain. The GLP-1 receptor has been found predominantly in insulinomas, gastrinoma, pulmonary neuroendocrine tumors, and medullary thyroid cancer. GLP-1 analogues have been synthesized for the GLP-1 receptor targeting, from which exendin-4 as an agonist and exendin-3 as an antagonist have been widely studied (Table 10). neuroendocrine tumors, and medullary thyroid cancer. GLP-1 analogues have been synthesized for the GLP-1 receptor targeting, from which exendin-4 as an agonist and exendin-3 as an antagonist have been widely studied (Table 10).

RGD Analogues for Integrin Receptors Imaging
Nowadays, over 20 subtypes of integrin family receptors are known, from which αvβ3, but also αvβ5 and αvβ6 are of well-studied subtypes recognizing the Arg-Gly-Asp (RGD) peptide (Figure 16), and their expression correlates with metastasis.

RGD Analogues for Integrin Receptors Imaging
Nowadays, over 20 subtypes of integrin family receptors are known, from which α v β 3 , but also α v β 5 and α v β 6 are of well-studied subtypes recognizing the Arg-Gly-Asp (RGD) peptide (Figure 16), and their expression correlates with metastasis.
An enhanced α v β 3 expression is associated with angiogenesis, tumor growth, invasion, and metastasis. The α v β 3 integrins expression has been demonstrated in various endothelial and cancer cells such as breast, gastric, non-small cell lung, pancreatic, ovarian, and prostate cancer, oral squamous cell carcinoma, melanoma, or glioma [167]. Over the last decades, many radiolabeled bioactive molecules with the RGD motif have been synthesized and evaluated for the integrin α v β 3 -positive tumors targeting, providing useful conjugates for clinical translation (see summary in Table 11). Since 2018, a number of traditional syntheses of novel BFCA-RGD conjugates has rapidly decreased due to the utilization of RGD peptides for a nanoparticle coupling. An enhanced αvβ3 expression is associated with angiogenesis, tumo sion, and metastasis. The αvβ3 integrins expression has been demonstra endothelial and cancer cells such as breast, gastric, non-small cell lung, pa ian, and prostate cancer, oral squamous cell carcinoma, melanoma, or Over the last decades, many radiolabeled bioactive molecules with the R been synthesized and evaluated for the integrin αvβ3-positive tumors tar ing useful conjugates for clinical translation (see summary in Table 11) number of traditional syntheses of novel BFCA-RGD conjugates has rap due to the utilization of RGD peptides for a nanoparticle coupling. Table 11. Summary of radiolabeled RGD analogues for αvβ3 receptor-positive tumor imaging over past 3   Table 11. Summary of radiolabeled RGD analogues for α v β 3 receptor-positive tumor imaging over past 3 years. -preclinical in vitro, in vivo -prostate -PET -significant limitations due to high renal and bladder accumulation, but low uptake in other organs [172]  -clinical, 20 patients -breast -gamma camera -good uptake in breast lesions and also metastatic sites in lymph nodes visible in 2 patients -useful easily available kit for further clinical studies [173] -68 Ga -DOTA -glutamic acid -(cRGDfK)2 -preclinical in vitro, in vivo -lung -PET/CT -68 Ga-labeled conjugate with highly hydrophilic properties, high tumor accumulation, moderate in vivo uptake in kidneys and intestine, with a potential for early detection of lung lesions [174]

Other Radiometal Labeled Peptide Analogues for Imaging of Other Tumor Receptors
Neurotensin (NT), α-melanocyte stimulating hormone (α-MSH), substance P, and vasoactive intestinal peptide (VIP) represent other important radiometal labeled peptide analogues for imaging of various other significant tumor receptors ( Figure 17). -preclinical in vitro, in vivo -prostate -PET -significant limitations due to high renal and bladder accumulation, but low uptake in other organs [172] -99m Tc -HYNIC, tricine, TPPTS -x -RGD2 -clinical, 20 patients -breast -gamma camera -good uptake in breast lesions and also metastatic sites in lymph nodes visible in 2 patients -useful easily available kit for further clinical studies [173] -68 Ga -DOTA -glutamic acid -(cRGDfK)2 -preclinical in vitro, in vivo -lung -PET/CT -68 Ga-labeled conjugate with highly hydrophilic properties, high tumor accumulation, moderate in vivo uptake in kidneys and intestine, with a potential for early detection of lung lesions [174] 4. 6

. Other Radiometal Labeled Peptide Analogues for Imaging of Other Tumor Receptors
Neurotensin (NT), α-melanocyte stimulating hormone (α-MSH), substance P, and vasoactive intestinal peptide (VIP) represent other important radiometal labeled peptide analogues for imaging of various other significant tumor receptors ( Figure 17). The NT is a neurotransmitter and hormone with a sequence of 13 AA, in which the C-terminal NT(8-13) is responsible for affinity and activity to a NT receptor. There are three types of the NT receptors: NTR1-NTR3, where NTR1 is an extensively studied receptor and a promising target for cancer imaging. The NTR1 overexpression has been demonstrated in a tumor progression, e.g., in pancreas and colon adenoma, but also in breast, lung, or prostate cancer, while the expression of NTR2 has been reported in prostate cancer, lymphatic leukemia, and glioma [175]. Several NT analogues have been developed as effective targets for colorectal adenocarcinoma cells (Table 12).
The α-MSH is a neuropeptide with a sequence of 13 AA that is selectively bound to a melanocortine-1 receptor (MC1) overexpressed in leukocytes, melanocytes, and transformed melanoma cells, and is primarily responsible for a regulation of inflammatory state and skin pigmentation [176]. Numerous α-MSH analogues have been developed as attractive targets for melanoma radiodiagnosis or imaging (Table 12). The NT is a neurotransmitter and hormone with a sequence of 13 AA, in which the C-terminal NT(8-13) is responsible for affinity and activity to a NT receptor. There are three types of the NT receptors: NTR 1 -NTR 3 , where NTR 1 is an extensively studied receptor and a promising target for cancer imaging. The NTR 1 overexpression has been demonstrated in a tumor progression, e.g., in pancreas and colon adenoma, but also in breast, lung, or prostate cancer, while the expression of NTR 2 has been reported in prostate cancer, lymphatic leukemia, and glioma [175]. Several NT analogues have been developed as effective targets for colorectal adenocarcinoma cells (Table 12).
The α-MSH is a neuropeptide with a sequence of 13 AA that is selectively bound to a melanocortine-1 receptor (MC1) overexpressed in leukocytes, melanocytes, and transformed melanoma cells, and is primarily responsible for a regulation of inflammatory state and skin pigmentation [176]. Numerous α-MSH analogues have been developed as attractive targets for melanoma radiodiagnosis or imaging (Table 12).
The substance P with a 11-AA sequence belongs to a family of tachykinins and exerts its activity through the G protein-coupled neurokinin receptors (NKR), i.e., NK 1 R-NK 3 R, with the highest affinity of NK 1 R. The substance P has been found in various cell systems bearing NK 1 R, such as immune cells, monocytes, macrophages, lymphocytes, microglia, dendritic cells, bone marrow stem cells, and others. In the central nervous system, NK 1 R are expressed in neurons, astrocytes, microglia, and cerebral endothelial cells [177]. Effects of the substance P in human organism include: immune and secretion stimulation, smooth muscle contraction (pulmonary, urinary, GIT, and vascular system), and is involved also in a pain transmission, vasodilatation, connective-tissue cell proliferation, and neuroimmune modulation [177]. Thus, substance P analogues and NK 1 R antagonists have been synthesized and used for the NK 1 R-positive tumor detection as shown in Table 12.
The VIP is a peptide with a 28 AA sequence that regulates various immune cells, promotes vasodilatation, growth and function of tumor cells. Its biological action is mediated through three classes of the G-protein-coupled receptors VPAC1, VPAC2, and PAC1. The receptors for VIP occurs in numerous tumor cells including thyroid, breast, lung, liver, pancreas, intestinal epithelial cells, colon, bladder, prostate, uterus, and neuroendocrine tumors [178,179]. Table 12. Summary of radiolabeled NT, α-MSH, substance P, and VIP analogues for other important receptor-positive tumor imaging over past 3 years.

Small Peptide Inhibitors of Proteins for Protein-Positive Tumor Imaging
Many protein interactions in a biological system are responsible for an origination or progression of various diseases including cancer. In recent years, inhibitors of such proteins based on small peptide biomolecules are widely developed and investigated. This subsection covers the latest radiolabeled peptide inhibitors of the prostate-specific membrane antigen (PSMA) and fibroblast activation protein (FAP) for imaging of related tumors (see summarized studies in Table 13).
The PSMA is a membrane-bound folate gamma glutamyl-carboxypeptidase II, which is physiologically present in various tissues, e.g., salivary glands, ovary, prostate epithelium, and astrocytes [191]. From the cancerous cells, it is primarily expressed in benign and malignant prostatic tissue [192]. However, studies on the PSMA-expression in also other tumor types are available, including breast, gastric, and colorectal cancer, lung and renal carcinoma, and brain tumors [193][194][195][196][197][198]. Thus, PSMA has become one of the most promising and extensively evaluated molecular targets in nuclear medicine. Research was mainly focused on monoclonal antibodies, but various radiolabeled small peptide-based inhibitors containing Glu-C(O)-Lys (EuK) sequence (see Figure 18A) have been recently developed to effectively localize and treat related tumors. Other two functionalities, i.e., phosphonates and thiols, with affinity to PSMA have been identified. The most widely used example of such inhibitor is the [ 68 Ga]Ga-PSMA-11 (i.e., 68 Ga-labeled Glu-NH-CO-NH-Lys(Ahx)-HBED-CC) [199]. At present, it is included in many clinical trials that monitor various conditions in a prostate cancer management.
Another extensively studied protein with selective expression in several tumor types is FAP, a serine protease. The FAP protein has been associated with fibrosis, inflammation and cancer, and is undetectable in a majority of normal adult tissues [200]. Several works revealed its localization not only in activated fibroblasts [201], but also in endothelial cells and macrophages [202,203]. The participation of FAP in a cell invasiveness, proliferation, migration and tumor vascularization has been described [204]. The FAP overexpression and activation has been observed in various malignancies, e.g., pancreatic, hepatocellular, lung, breast, colorectal, or ovarian [205][206][207][208][209][210]. Different strategies are investigated to target FAP activity such as (i) probes with fluorescent moiety, (ii) prodrug delivery systems, (iii) FAP inhibitors (FAPI), and (iv) immune-based pathways [211]. Radiolabeled peptide FAPI based on 2-cyanopyrrolidin-quinoline carboxamide structure ( Figure 18B) were developed [212] and then FAPI linkers have been modified to improve pharmacokinetic properties, tumor binding, and PET images [213]. Further structural modifications and clinical studies are underway and thus FAPI represent new attractive imaging and therapeutic options for oncological diseases.
Glu-NH-CO-NH-Lys(Ahx)-HBED-CC) [199]. At present, it is included in many clini trials that monitor various conditions in a prostate cancer management.
Another extensively studied protein with selective expression in several tum types is FAP, a serine protease. The FAP protein has been associated with fibrosis, flammation and cancer, and is undetectable in a majority of normal adult tissues [20 Several works revealed its localization not only in activated fibroblasts [201], but also endothelial cells and macrophages [202,203]. The participation of FAP in a cell invasiv ness, proliferation, migration and tumor vascularization has been described [204]. T FAP overexpression and activation has been observed in various malignancies, e pancreatic, hepatocellular, lung, breast, colorectal, or ovarian [205][206][207][208][209][210]. Different stra gies are investigated to target FAP activity such as (i) probes with fluorescent moiety, prodrug delivery systems, (iii) FAP inhibitors (FAPI), and (iv) immune-based pathwa [211]. Radiolabeled peptide FAPI based on 2-cyanopyrrolidin-quinoline carboxami structure ( Figure 18B) were developed [212] and then FAPI linkers have been modifi to improve pharmacokinetic properties, tumor binding, and PET images [213]. Furth structural modifications and clinical studies are underway and thus FAPI represent n attractive imaging and therapeutic options for oncological diseases.

Radiometal Labeled Sulfonamide-Based Analogues for Tumor Hypoxia Imaging
Hypoxia, a phenomenon when a level of oxygen is below its demands, is a common feature for tumor development and progression. Many solid tumors have regions permanently or transiently exposed to hypoxia because of aberrant vascularization and a poor blood supply [231]. Since hypoxia is a key component in cellular expression, tumor blood vessel formation, cancer progression, metastasis, often leading to cell death, a current research in this area is focused to an early detection and selective monitoring or suppression of hypoxic tissues to effectively minimize all possible complications associated with this phenomenon. Many studies have been comprised of radiolabeled small nitroimidazole derivatives [232][233][234][235], and monoclonal antibodies [236,237], resulting in a development of new agents capable of accessing to overexpressed proteins under hypoxic state (i.e., hypoxia inducible factor HIF-1 regulated genes for carbonic anhydrase CA IX, vascular endothelial growth factor, angiopoietin-2, etc. [238]). Nevertheless, small sulfonamideand peptide-based biomolecules labeled with metal radionuclides have been studied for imaging of various hypoxic tumor cells overexpressing CA IX as one of the prominent gene in the HIF-induced processes (see summary in Table 14). A highly specific binding of various sulfonamide derivatives with amino-acid substituents has been demonstrated in our several recent works. For example, an illustrative superposition and intermolecular interaction diagram of potential 1,3,5-triazinyl-sulfonamide inhibitor docked into the active site of human CA IX are in Figure 19A,B.

Concluding Remarks and Future Perspectives
Various chemical types of metallic radiopharmaceuticals for use in oncology are approved by the European Medicines Agency or U.S. Food and Drug Administration. Apart from these registered radioactive medicines, a much larger scale of radiolabeled bioactive ligands is under investigation in nuclear research or clinical trials. In this review, recent advances in the radiolabeling process of amino-acid based biomolecules, the most commonly used metal radionuclides, their chemistry and BFCA, as well as the most important peptide receptor families (including currently the most perspective field of PSMA and FAP ligands), were critically discussed. Continual efforts in proposing new structures with improved pharmacokinetic properties for selective targeting of cancer cells and effective utilization in imaging techniques should be guaranteed. The disease imaging on a molecular level, as well as radionuclide availability on-site, lower radiation burden, detection of early stage problem, and monitoring of a response to treatment in the combination with targeted therapy for a personalized approach to a patient, have a great potential to bring additional valuable outputs in the field of nuclear medicine in future.
Over the past years, great progress in a radiolabeling with metallic radionuclides has been demonstrated, owing to a development of many new chelators (or new derivatives of well-known traditional chelators) and linkers for an effective connection between metals and biomolecules. Modern chelators such as TRAP, THP, and FSC for gallium-68, DFO for zirconium-89, sarcophagines for copper-64, tricarbonyl and [N,S,X]-type chelators for technetium-99m and their modifications have been designed to improve binding affinity and pharmacokinetic properties of a radiolabeled probe for its molecular target. In spite of remarkable progress, there is still an enormous need to develop target specific compounds with improved pharmacokinetics and selectivity to a desired in vivo target, because many studies have confirmed various complications in the development. These are mainly lower stability, higher toxicity, adverse pharmacokinetic behavior, and higher retention of radioactivity in studied material in vivo and in vitro. In this context, amino acid moieties proved to be ones of the most suitable linkers to complete a target-specific structure. Optimized structures of some of the newly developed radiolabeled biomolecules should provide enhanced affinity and selectivity to the onco-receptors, lower radiation dosage for patient, decreased interactions with other drugs or physiological proteins, without misrepresenting results, and, by that, a more favorable utilization in diagnostic nuclear medicine over other imaging techniques (e.g., MRI, CT).
Peptides, as amino acid based biomolecules, represent current and future important tools in a development of target-specific radiolabeled compounds. It is due to a high degree of their compatibility with many protein structures overexpressed in various diseases, including cancer, as the second leading cause of death globally. Current research, with a promising perspective, is directed mainly towards peptide radiolabeled agents that are aimed at proteins overexpressed in pancreatic, colorectal, prostate, and brain tumors. These types belong to the most frequently diagnosed and the most severe cancers. The integrin α v β 3 receptors from traditional receptor families and PSMA, as well as FAP ligands are very attractive and perspective probes due to their intense association and overexpression within a variety of cancer cells and new vasculature in general, and so tumor growth, proliferation, and metastasis.
As emerged from the reviewed studies dealing with an implementation of imaging methods (PET, SPECT, etc.), in nuclear medicine research, gallium-68, DOTA-based chelators, and amino acid linkers are currently dominating in the research of new potential diagnostic and imaging agents. In centers, where 68 Ga-compounds cannot be used due to gallium unavailability, alternative PET labels were introduced. For example, yttrium-86 or zirconium-89 could be employed since a remarkable development in small medical cyclotrons has been achieved over past years. However, there are still new 99m Tc-labeled analogues for SPECT imaging as an alternative method of PET tracers. Other interesting non-standard radionuclides such as cobalt-55, scandium-44, titanium-45, and manganese-52 are increasingly utilized in preclinical studies and could be a merit of future investi-gations in clinical field. These non-standard metal radionuclides with their therapeutic pairs represent the highly attractive labels for development of theranostic approaches as precise predictive biomarkers of a response to therapy strategies. The inherent part of a diagnostic or imaging process is an applied imaging technique. It is evident that hybrid methods of SPECT and PET combined with CT is of routine. The ongoing studies could be focused on a development of probes and methodologies with high anatomical and functional sensitivity, spatial resolution, as well as mentioned superior pharmacokinetic profile for a better disease management using SPECT and PET with MRI as an important tool to improve the diagnostics, staging and planning of treatment strategy.