Next Article in Journal
FLIP the Switch: Regulation of Apoptosis and Necroptosis by cFLIP
Next Article in Special Issue
Combination Treatment with Sublethal Ionizing Radiation and the Proteasome Inhibitor, Bortezomib, Enhances Death-Receptor Mediated Apoptosis and Anti-Tumor Immune Attack
Previous Article in Journal
Oxidative Stress and Inflammation in Hepatic Diseases: Therapeutic Possibilities of N-Acetylcysteine
Previous Article in Special Issue
Histone H2AX Is Involved in FoxO3a-Mediated Transcriptional Responses to Ionizing Radiation to Maintain Genome Stability
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:

Human Anti-Oxidation Protein A1M—A Potential Kidney Protection Agent in Peptide Receptor Radionuclide Therapy

Section for Infection Medicine, Department of Clinical Sciences in Lund, Lund University, Lund 221 84, Sweden
Lund University Bioimaging Center, Lund University, Lund 221 84, Sweden
Section of Medical Radiation Physics, Department of Clinical Sciences in Lund, Lund University, Lund 221 84, Sweden
Author to whom correspondence should be addressed.
Int. J. Mol. Sci. 2015, 16(12), 30309-30320;
Submission received: 31 October 2015 / Revised: 28 November 2015 / Accepted: 11 December 2015 / Published: 18 December 2015
(This article belongs to the Collection Radiation Toxicity in Cells)


Peptide receptor radionuclide therapy (PRRT) has been in clinical use for 15 years to treat metastatic neuroendocrine tumors. PRRT is limited by reabsorption and retention of the administered radiolabeled somatostatin analogues in the proximal tubule. Consequently, it is essential to develop and employ methods to protect the kidneys during PRRT. Today, infusion of positively charged amino acids is the standard method of kidney protection. Other methods, such as administration of amifostine, are still under evaluation and show promising results. α1-microglobulin (A1M) is a reductase and radical scavenging protein ubiquitously present in plasma and extravascular tissue. Human A1M has antioxidation properties and has been shown to prevent radiation-induced in vitro cell damage and protect non-irradiated surrounding cells. It has recently been shown in mice that exogenously infused A1M and the somatostatin analogue octreotide are co-localized in proximal tubules of the kidney after intravenous infusion. In this review we describe the current situation of kidney protection during PRRT, discuss the necessity and implications of more precise dosimetry and present A1M as a new, potential candidate for renal protection during PRRT and related targeted radionuclide therapies.

1. Peptide Receptor Radionuclide Therapy (PRRT)

1.1. Background

Neuroendocrine tumors (NETs) are a large group of neoplasms derived from the neuroendocrine system. Common sites for primary tumors are the gastrointestinal tract, the lungs, and other neuroendocrine tissues [1,2]. In the 1980s it was discovered that some tumors overexpress peptide receptors. The somatostatin receptor family consists of five receptor subtypes, sstr1-5 [3]. A majority of NETs has a strong over-expression of somatostatin receptors, mainly subtype 2 (sstr2), which is the key target for therapy using stable somatostatin analogues (SSA) [3]. Peptide receptor radionuclide therapy (PRRT) using somatostatin analogues such as octreotide chelated to β-emitting radionuclides (177Lu, 90Y) have been successfully used to target inoperable or metastatic NETs for the past 15 years. A large body of evidence describes the effectiveness and clinical safety of these procedures [3]. PRRT as a therapeutic option, has proven ideal for patients expressing well or moderately differentiated neuroendocrine carcinomas of grade 1 or 2, since these tumors often have metastasized and are inoperable. The first attempt to evaluate the diagnostic compound 111In-octreotide as a potential radiopharmaceutical took place in the 1990s, with patients receiving cumulative activities of at least 20 and up to 160 gigabecquerel (GBq; activity unit for radioactivity 1 Bq equal to one decay per second). Therapeutic effects could be demonstrated: partial and minor remission and stabilization of progressive tumors in half of the patients [4]. Side effects consisted of mild bone marrow toxicity and leukemia with absorbed doses to the bone marrow in the order of 3 Gray (Gy). However, the failure of the therapy in many patients can be explained by the short range of the emitted electrons (mainly Auger electrons) in combination with heterogeneous receptor expression (equal to activity distribution) in the NETs. Because of this, 111In-based therapy is generally not recommended for PRRT [5]. Although 111In-octreotide infusion to this day remains a therapeutic option for NETs, it has been replaced by conjugates with β-emitters such as 90Y and 177Lu.
PRRT utilizing the two radiopharmaceuticals 90Y-[DOTA0, Tyr3]-octreotide (DOTATOC) and 177Lu-[DOTA0, Tyr3]-octreotate (DOTATATE) has proven to be an effective and safe alternative treatment for patients with metastatic NETs [6,7]. Both peptides are derivatized somatostatin analogues that show high affinity for sstr2. DOTATATE has a higher affinity for sstr2 (1.5 ± 0.4 nM) when compared to DOTATOC (14 ± 2.6 nM), but does not display any affinity for other subtype receptors such as sstr3 and sstr5 [8]. DOTATOC has a weak, but non-negligible affinity, for sstr3 and sstr5 (393 ± 84 nM and 880 ± 324 nM respectively) [9].
DOTATATE has been shown to perform favorably compared to alternative treatment modalities in terms of tumor response rate and progression-free survival with a survival benefit of 40–72 months when compared to controls [10]. A recent large international multi-center trial [11] has shown marked improvement in progression-free survival rate and overall survival in patients undergoing PRRT with DOTATATE.

1.2. Diagnostic Assessment

The WHO recently published a three-tiered classification system for NETs based on their mitotic rate and Ki-67 index: NET Grade 1, NET Grade 2, and neuroendocrine carcinoma [12]. Patients with NET grade 1 or 2 (low grade carcinomas) are ideal candidates for PRRT. The sstr2-expressing NETs in the bronchial and gastroenteropancreatic tract are the most common NETs considered for PRRT with radiolabeled somatostatin analogues [3]. Other NETs, such as medullary thyroid carcinoma, phaeochromocytoma, paraganglioma and neuroblastoma, are also highly suitable candidates for PRRT [13,14,15,16,17,18].
In order to select viable candidates that would benefit from PRRT it is important to assess sstr-status. Functional imaging with single photon emission computed tomography (SPECT) using 111In-pentetreotide and positron emission tomography (PET) with 68Ga-labaled SSA are well established methods to assess sstr status and collect essential information for staging and re-staging [19,20]. In particular, PET has proven superior to SPECT, providing a more accurate, personalized treatment [21]. A detailed anatomical imaging of the primary tumor and its metastases can be obtained utilizing computed tomography (CT), ultrasonography and magnetic resonance imaging (MRI) and is important to evaluate treatment response [3].
Contraindications for PRRT treatment include pregnancy, acute concomitant diseases, and psychiatric disorders [3]. Other considerations are compromised bone marrow or severely compromised renal function, although patients with the latter can still be considered for treatment.

1.3. Dose-Limiting Organs

The bone marrow and the kidneys are both dose-limiting organs in PRRT-therapy, and the latter is considered to be the major dose-limiting organ [22,23]. As there is physiological renal retention of radiolabeled somatostatin analogues, the cumulative kidney absorbed dose limits the possible activity to administer. If one can reduce the toxicity to normal tissues (mainly the kidneys), the therapeutic window can be enlarged. Radiolabeled somatostatin analogues are filtered by the glomeruli and reabsorbed in the proximal tubules. The megalin/cubulin system plays an essential role in the reabsorption of octreotide. Reduction of the renal uptake can be achieved during PRRT by infusion of the positively charged amino acids l-lysine and l-arginine [3].

2. Dosimetry

Because of the unwanted uptake in the kidneys and other non-target tissues, precise and reliable dosimetry is needed to optimize PRRT. Absorbed dose is defined as imparted energy per mass unit (1 J/kg equals 1 Gy). The imparted energy causes ionizations and excitations inducing damage to biological molecules due to direct or indirect effects. The latter process include reactions with free radicals that are generated as a result of interaction with water molecules. Examples of direct and indirect effects of the deposited energy in biological tissue are oxidations and radical formations of cellular molecules, causing single strand (SSB) and double strand breaks (DSB) of nuclear DNA.
In vivo dosimetry requires knowledge of the kinetics of the radiopharmaceutical. However, the determination accuracy of the radioactivity distribution in imaging techniques such as SPECT and PET becomes limited. For example, the quantitative uncertainty is 2% or more using SPECT [24].
In conventional external radiotherapy, an absorbed dose of 23 Gy to the whole kidney gives an expected risk of 5% of nephrotoxicity within five years [25]. This cannot be applied directly to PRRT due to the lower dose rate where absorbed doses of 27–29 Gy are tolerated. For the bone marrow a maximal absorbed dose of 2 Gy is generally acceptable. This emphasizes the importance of individualized kidney and bone marrow dosimetry, in order to predict and circumvent toxicity and maximize the absorbed dose to the tumor. A threshold biological effective dose (BED) to the kidneys for patients with no risk factors has been evaluated by Bodei et al. [22] to 40 Gy. While a maximum BED of 28 Gy to the kidneys is recommended, the same author states that further investigation is needed to determine a more definite threshold BED.
The varying activity distributions within the kidney affect the absorbed dose distribution. High-energy β emission from 90Y results in a fairly homogeneous absorbed dose distribution, whereas low-energy electron (Auger electron) and medium energy β emitters as 111In and 177Lu give more inhomogeneous absorbed dose distributions. As a consequence in PRRT, a higher absorbed dose can be seen in cortical nephrons and in the juxtamedullary zone.
Guidelines on how individualized patient dosimetry in radionuclide therapy can be performed are found in the literature [26,27]. The relative activity distribution in vivo is quantifiable by SPECT and PET. With a pure, low energy β emitter this activity concentration can simply be transformed to an absorbed dose rate by multiplying with an absorbed dose conversion factor. If a substantial fraction of the decay energy is released as photons or high energy β particles, radiation cross-fire has to be considered.
In most cases dosimetry is performed using the Medical Internal Radiation Dose (MIRD)-concept calculating mean absorbed dose D, with standardized human anatomy. The MIRD scheme is in a simplified way written as
D = Ã × S = A 0 × τ × S
where à is the cumulated activity and S is the mean absorbed dose per cumulated activity (or S-factor), which depends on the properties of target organs and the radionuclide used. Several numerical or compartment models are used to calculate à and dedicated software such as OLINDA is then used to calculate the absorbed dose [28,29]. Patients with known risk factors can benefit from patient specific dosimetry, where the cumulated dose is determined from a series of scintillation camera measurements using either planar scintigraphy or SPECT. Reported absorbed dose range per unit activity to the kidneys for 90Y-DOTATOC and 177Lu-DOTATATE treatments are 2.55–2.84 Gy/GBq and 0.62–0.9 Gy/GBq, respectively (Table 1) [3].
Table 1. Three examples of reported absorbed doses in kidneys per unit activity (Gy/GBq) with mean ± SD or median range (marked with an asterisk) following PRRT utilizing 90Y-DOTATOC and 177Lu-DOTATATE.
Table 1. Three examples of reported absorbed doses in kidneys per unit activity (Gy/GBq) with mean ± SD or median range (marked with an asterisk) following PRRT utilizing 90Y-DOTATOC and 177Lu-DOTATATE.
Absorbed dose per unit administered activity2.84 ± 0.640.88 ± 0.19
2.44 (1.12–4.5) *0.62 (0.45–17.74) *
2.73 ± 1.410.9 ± 0.3
* median (range).
Based on the kidney anatomy, a detailed dosimetry model has been developed by the Committee on Medical Internal Radiation Dose (MIRD). Here, regional S-factors can be derived and used in the case of heterogeneous activity distribution [30].
It has been reported that high energy β emitters as 90Y can be accurately described by the MIRD kidney dosimetry approach whereas low energy emitters as 111In and 177Lu need dosimetry calculations based on autoradiography activity distributions [25].

2.1. PRRT—Side Effects and Protective Measures

Acute side effects, such as headaches, nausea, and vomiting occur in the majority of patients [31]. These side effects can be ameliorated with hydration and antiemetic treatment. Delayed side effects are closely related to the dose limiting organs and include loss of renal function, especially in patients with severe hypertension, diabetes mellitus, and bone marrow toxicity [18].
Most of the radiolabeled somatostatin analogs are cleared by the kidneys and the majority of the activity is excreted via the urine. However, a small amount (about 2%) is reabsorbed and retained in the proximal tubuli and prolonged irradiation of the kidneys follows. To inhibit the uptake in the proximal tubule protective measures are taken by infusing positively charged amino acids such as l-lysine and/or l-arginine. These countermeasures have proven to significantly reduce the renal absorbed dose and are widely used today.
Despite protective measurements, loss of renal function has been observed in patients undergoing PRRT. It has been observed that patients with NETs treated with 177Lu-DOTATATE or 90Y-DOTATOC suffered a creatinine clearance loss of 3.8% and 7.3%, respectively, per year [3]. The infusion of basic amino acids has also been reported to potentially cause acute hyperkalemia as well as being a potential catalyst for hormonal crisis in patients undergoing PRRT [32,33].
The search for methods that could reduce renal uptake and mitigate radiation induced damage requires extensive knowledge of uptake mechanisms, kinetic properties of the protective agents, and their distribution in target organs and other tissues.
The cytoprotective agent amifostine has demonstrated protective properties. In vivo experiments with rats showed a significant decrease in renal uptake [34]. To further increase protection, the combined infusion of amifostine and l-lysine has been suggested in order to cover both long and short-term effects.

2.2. Kidney Activity Distributions

Autoradiography of resected kidneys from patients administered 111In-DTPA-Octreotide has revealed irregular distribution of activity in the cortex with highest uptake around the juxtamedullary cortex region [25]. It was also reported that the medulla showed heterogeneous activity distribution with highest activities in the central parts.
To fully understand the biological effect of the heterogeneous activity distribution and corresponding absorbed dose distribution, the cellular and subcellular pattern need to be revealed. In the study from Ahlstedt et al. [35] it was shown that a fluorescence-labeled octreotide-derivate was localized preferentially to the kidney cortex in tubular epithelial cells (See Figure 1 for more details).
Figure 1. Visualizing the distribution of 125I-labelled A1M 20 minutes post-injection at different magnification using SPECT/CT (A) and digital autoradiography (B) at the organ-level and fluorescence imaging showing both A1M (green), octreotide (red) and cell nuclei (blue) (C,D) at cellular and sub-cellular levels. The arrow in (D) indicates one single cell. The figure is modified from reference 35 with permission from the publisher.
Figure 1. Visualizing the distribution of 125I-labelled A1M 20 minutes post-injection at different magnification using SPECT/CT (A) and digital autoradiography (B) at the organ-level and fluorescence imaging showing both A1M (green), octreotide (red) and cell nuclei (blue) (C,D) at cellular and sub-cellular levels. The arrow in (D) indicates one single cell. The figure is modified from reference 35 with permission from the publisher.
Ijms 16 26234 g001
Assuming a mean absorbed dose to the cortex of 27 Gy, local maximum absorbed doses for 177Lu, 111In, and 90Y have been reported to be 47, 40, and 25 Gy respectively [25]. Furthermore, the JM complex has been reported to receive absorbed doses of 39 Gy for 111In-DTPA-octreotide and 32 Gy for DOTATOC with an average kidney absorbed dose of 27 Gy. For DOTATATE an average kidney absorbed dose of 23 Gy can result in an absorbed dose of 40 Gy to the JM complex [25].

3. Oxidative Stress

3.1. Oxidation and Antioxidation

The term “oxidative stress” is used to describe physiological conditions with an abnormally high production of redox active compounds and/or impaired antioxidative tissue defense systems [36]. Mediators of oxidative stress are reactive oxygen species (ROS) including free radicals, which are highly reactive due to the presence of unpaired electrons. ROS and radicals react with proteins, DNA, membranes etc, which can lead to unwanted modifications of the target molecules and loss of their functions. Endogenous generators of oxidative stress are hemoglobin (Hb) and heme, released during hemolysis [37] and other heme-proteins such as cytochrome c and myoglobin, released during inflammation and tissue necrosis. Mitochondrial respiration also generates ROS, and is a source of oxidative stress during inflammation and tissue necrosis.
Physiological defense systems have evolved to counteract the chemical threat of oxidative stress to exposed tissues and macromolecules. ROS and other oxidative compounds are inhibited and eliminated by antioxidation enzymes such as superoxide dismutase (SOD), glutathione peroxidase (Gpx), and catalase [38,39,40]. Free Hb and heme in blood are bound by haptoglobin and hemopexin, and cleared by specific receptors in macrophages and liver [41]. Intracellular heme is bound and degraded by heme oxygenase (HO) [42].

3.2. Radiation and Oxidative Stress

Irradiation of biological tissues, such as in PRRT, leads to induction of oxidative stress. Thus, as described above, ROS and free radicals are generated by (1) direct interactions between the irradiation particles and molecules of the targeted biological tissue; and (2) secondary interactions between components released from the directly irradiated dead cells and surrounding cells and matrix molecules. The latter, secondary, response is also referred to as the “bystander effect”, i.e., the irradiation causes damage to cells and tissues which are surrounding the targeted areas, but are not directly hit [43,44,45].

3.3. α1-Microglobulin (A1M)

3.3.1. Structure, Expression, and Distribution

α1-Microglobulin (A1M) is a recently discovered physiological antioxidant, active both inside cells and in the extracellular compartments [46,47]. It is conserved in evolution and found in all vertebrates including birds and fish. A1M is a 26 kDa glycoprotein that belongs to Lipocalin protein family [48,49]. The Lipocalins are a group of >50 structurally related proteins in bacteria, plants, and animals, and are believed to originate from a common ancestor. They are one-domain proteins with a 150–190 amino acid-polypeptide and a common fold that consists of an eight-stranded β-barrel with a closed bottom and an open end at the top. The interior of the barrel usually serves as a binding site for mostly hydrophobic low molecular weight ligands [48]. The archetype lipocalin is retinol-binding protein (RBP) which transports vitamin A (retinol) in blood [50]. The structure of the major part of A1M was recently reported [51] and is shown in Figure 2.
Figure 2. Three-dimensional rendering of A1M based on the published crystal structure [51]. The position of the C34 group (mutated to serine in the crystal structure) is highlighted in red. This is the critical site for the reductase, heme binding, and radical scavenging properties of A1M.
Figure 2. Three-dimensional rendering of A1M based on the published crystal structure [51]. The position of the C34 group (mutated to serine in the crystal structure) is highlighted in red. This is the critical site for the reductase, heme binding, and radical scavenging properties of A1M.
Ijms 16 26234 g002
The major site of synthesis of A1M is the liver [52], but all other investigated organs and cells express the protein although at a lower rate. The gene of A1M is denoted the α1-Microglobulin-Bikunin Precursor (AMBP) gene and encodes a continuous precursor protein consisting of A1M and bikunin, which are linked together during translation and in the ER lumen, but cleaved in the Golgi and secreted as two separate proteins with different functions [53,54]. Bikunin is a protease inhibitor and matrix component [55]. The co-synthesis is conserved in all cells and all species and the functional significance of the peculiar expression arrangement is yet unknown.
After secretion to the blood, A1M is rapidly extravasated and found in the extravascular compartment in most organs. Thus, a rapid equilibrium between intra- and extravascular compartments (T1/2 in blood = 2–3 min) is established [56] and a steady state concentration of 1–2 µM A1M in the plasma is achieved [57]. A1M is found both in a monomeric form and complex-bound to IgA, albumin, and prothrombin [58]. Being a small protein, A1M is equally quickly filtrated by the glomeruli of the kidneys and reabsorbed by the proximal tubule epithelial cells. Small amounts, however, escape this route and are excreted into the urine, amounting to approximately 5 mg/24 h [59].

3.3.2. Biochemical Properties, Physiological Function, and Therapeutic Applications

A1M has been shown to have heme-binding, radical scavenging, and reductase properties [47] that suggest a physiological role as an antioxidant. Heme-groups can be bound by A1M [60,61] and proteolytic removal of a C-terminal tetrapeptide induces a pseudoenzymatic heme-degradation activity [60]. The free thiol group in amino acid position C34 (Figure 2) is the active site of a reductase/dehydrogenase activity of A1M [62]. Enzymatic reduction of free iron, heme proteins, and oxidized matrix and cytosolic proteins have been shown [62,63,64]. The reduction potential of the C34 thiol group also constitutes the structural and enzymatic basis of a radical binding mechanism that leads to covalent trapping of free radicals to lysyl and tyrosyl side-chains of A1M [65]. In line with this, human urine and amniotic A1M were shown to be yellow-brown due to covalent modifications [46,66,67].
As suggested by these biochemical properties of A1M, the protein has an antioxidant function in physiological situations with elevated oxidative stress. This has been verified in several reports that demonstrate that A1M can protect in vitro cell and organ cultures against oxidative damage from Hb, heme, and ROS [63,68,69]. Adding to the antioxidation potential in vivo, A1M was shown to accumulate in mitochondria via binding to mitochondrial Complex I stabilizing mitochondrial structure and maintaining ATP production during oxidative stress [70]. Also, upregulation of the AMBP-gene by elevated concentrations of ROS, hemoglobin and heme was reported in vitro and in vivo, suggesting an increased antioxidative protection potential during physiological oxidative stress [71,72].
A probable role as a radical- and hemescavenging antioxidant has led to the proposal of A1M as a therapeutic drug in diseases where elevated levels of Hb, heme and ROS constitute the major pathological insult [47]. Thus, infusion of A1M was shown to successfully treat placenta and kidney damage in the oxidative stress-related disease preeclampsia in vivo in sheep and rabbit models [73,74]. A1M could also inhibit glomerular damage induced by Hb-infusion in rats [75].

4. A1M in PRRT

4.1. A1M Protects against Radiation-Induced Tissue Damage

Two previous publications from our group demonstrate that A1M can protect bystander cells against irradiation-induced damage in vitro [64,76]. Using an experimental setup that allowed irradiation of a minor fraction of a human hepatoma monolayer, leaving the major part as bystander cells, it was shown that alpha-particle irradiation induced significant oxidative stress, cell death, apoptosis, and cell cycle arrest in the bystander cells. Addition of A1M to the culture medium reduced the cell death and inhibited apoptosis, oxidation biomarker formation, and upregulation of stress-response genes.

4.2. Infused A1M Is Localized to Kidneys in Vivo

To allow protection of radiation-exposed tissue-components in the kidneys during PRRT, a method to increase the concentration of A1M in kidney tissues should be developed. It was demonstrated several years ago that a large part (27%) of A1M was localized to the kidneys in rats in vivo 45 min. after intravenous (iv) infusion [56]. It was recently demonstrated in mice that exogenously infused A1M and the somatostatin-analogue octreotide, used clinically in PRRT, are co-localized in kidneys primarily in the proximal tubules, during the first hours after iv infusion [35]. Figure 2 illustrates the co-localization in the kidney cortex and on sub-cellular level in a proximal tubule after 20 min. In the study by Ahlstedt et al. [35] it was also shown that A1M appeared intact and full-length, suggesting that the protein still had functional activity.

4.3. Protection Hypothesis and Proof-of-Concept Experiments

The biological properties of A1M suggest that the protein may be employed as a co-treatment drug to protect against damaging side-effects on the kidneys during PRRT. Indeed, protection of kidney tissue from direct irradiation damage and/or bystander effects may allow a higher clinical dosage of the active peptides and hence a more efficient treatment of targeted tumors. This hypothesis is based on several sets of published results as described above. However, Proof-of-Concept experiments need to be performed to (1) ensure that kidney glomerular and tubular functions are significantly protected by A1M at various clinically relevant doses of radiopharmaceuticals while effects on tumors are maintained; (2) evaluate and optimize dosage regimen of both components. Such studies are presently undertaken at our laboratories.


This work was supported by grants from The Swedish Medical Research Council, Region Skåne (ALF), The Foundations of Crafoord, Greta and Johan Kock, and Österlund, A1M Pharma AB and the Swedish Cancer Foundation (CAN 15 0869), Mrs. Berta Kamprads Foundation. No particular funding to cover open access publication was obtained.

Author Contributions

Idea and drafting: Jonas Ahlstedt, Thuy A. Tran, Magnus Gram, Sven-Erik Strand and Bo Åkerström; Writing: Jonas Ahlstedt, Sven-Erik Strand and Bo Åkerström; Reviewing and commenting: Thuy A. Tran and Magnus Gram.

Conflicts of Interest

The authors Magnus Gram and Bo Åkerström are founders and share-holders of A1M Pharma. This does not alter the authors’ adherence to the policies of IJMS regarding sharing data and materials.


  1. Taal, B.G.; Visser, O. Epidemiology of neuroendocrine tumours. Neuroendocrinology 2004, 80, 3–7. [Google Scholar] [CrossRef] [PubMed]
  2. Modlin, I.M.; Lye, K.D.; Kidd, M. A 5-decade analysis of 13,715 carcinoid tumors. Cancer 2003, 97, 934–959. [Google Scholar] [CrossRef] [PubMed]
  3. Bodei, L.; Mueller-Brand, J.; Baum, R.P.; Pavel, M.E.; Horsch, D.; O’Dorisio, M.S.; O’Dorisio, T.M.; Howe, J.R.; Cremonesi, M.; Kwekkeboom, D.J.; et al. The joint IAEA, EANM, and SNMMI practical guidance on peptide receptor radionuclide therapy (PRRNT) in neuroendocrine tumours. Eur. J. Nucl. Med. Mol. Imaging 2013, 40, 800–816. [Google Scholar] [CrossRef] [PubMed]
  4. Valkema, R.; de Jong, M.; Bakker, W.H.; Breeman, W.A.; Kooij, P.P.; Lugtenburg, P.J.; de Jong, F.H.; Christiansen, A.; Kam, B.L.; de Herder, W.W.; et al. Phase I study of peptide receptor radionuclide therapy with (In-DTPA) octreotide: The rotterdam experience. Semin. Nucl. Med. 2002, 32, 110–122. [Google Scholar] [CrossRef] [PubMed]
  5. Kwekkeboom, D.J.; Krenning, E.P.; Lebtahi, R.; Komminoth, P.; Kos-Kudla, B.; de Herder, W.W.; Plockinger, U.; Mallorca Consensus Conference Participants; European Neuroendocrine Tumor Society. Enets consensus guidelines for the standards of care in neuroendocrine tumors: Peptide receptor radionuclide therapy with radiolabeled somatostatin analogs. Neuroendocrinology 2009, 90, 220–226. [Google Scholar] [CrossRef] [PubMed]
  6. Kam, B.L.; Teunissen, J.J.; Krenning, E.P.; de Herder, W.W.; Khan, S.; van Vliet, E.I.; Kwekkeboom, D.J. Lutetium-labelled peptides for therapy of neuroendocrine tumours. Eur. J. Nucl. Med. Mol. Imaging 2012, 39, S103–S112. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  7. Forrer, F.; Waldherr, C.; Maecke, H.R.; Mueller-Brand, J. Targeted radionuclide therapy with 90Y-DOTATOC in patients with neuroendocrine tumors. Anticancer Res. 2006, 26, 703–707. [Google Scholar] [PubMed]
  8. Maecke, H.R.; Reubi, J.C. Somatostatin receptors as targets for nuclear medicine imaging and radionuclide treatment. J. Nucl. Med. 2011, 52, 841–844. [Google Scholar] [CrossRef] [PubMed]
  9. Reubi, J.C.; Schar, J.C.; Waser, B.; Wenger, S.; Heppeler, A.; Schmitt, J.S.; Macke, H.R. Affinity profiles for human somatostatin receptor subtypes SST1-SST5 of somatostatin radiotracers selected for scintigraphic and radiotherapeutic use. Eur. J. Nucl. Med. 2000, 27, 273–282. [Google Scholar] [CrossRef] [PubMed]
  10. Kwekkeboom, D.J.; de Herder, W.W.; Kam, B.L.; van Eijck, C.H.; van Essen, M.; Kooij, P.P.; Feelders, R.A.; van Aken, M.O.; Krenning, E.P. Treatment with the radiolabeled somatostatin analog (177Lu-DOTA 0,Tyr3)octreotate: Toxicity, efficacy, and survival. J. Clin. Oncol. 2008, 26, 2124–2130. [Google Scholar] [CrossRef] [PubMed]
  11. Advanced Accelerator Applications. Available online: (accessed on 1 October 2015).
  12. Rindi, G. The enets guidelines: The new TNM classification system. Tumori 2010, 96, 806–809. [Google Scholar] [PubMed]
  13. Gains, J.E.; Bomanji, J.B.; Fersht, N.L.; Sullivan, T.; D’Souza, D.; Sullivan, K.P.; Aldridge, M.; Waddington, W.; Gaze, M.N. 177Lu-DOTATATE molecular radiotherapy for childhood neuroblastoma. J. Nucl. Med. 2011, 52, 1041–1047. [Google Scholar] [CrossRef] [PubMed]
  14. Bartolomei, M.; Bodei, L.; de Cicco, C.; Grana, C.M.; Cremonesi, M.; Botteri, E.; Baio, S.M.; Arico, D.; Sansovini, M.; Paganelli, G. Peptide receptor radionuclide therapy with (90)Y-DOTATOC in recurrent meningioma. Eur. J. Nucl. Med. Mol. Imaging 2009, 36, 1407–1416. [Google Scholar] [CrossRef] [PubMed]
  15. Iten, F.; Muller, B.; Schindler, C.; Rochlitz, C.; Oertli, D.; Macke, H.R.; Muller-Brand, J.; Walter, M.A. Response to ((90)Yttrium-DOTA)-TOC treatment is associated with long-term survival benefit in metastasized medullary thyroid cancer: A phase ii clinical trial. Clin. Cancer Res. 2007, 13, 6696–6702. [Google Scholar] [CrossRef] [PubMed]
  16. Bodei, L.; Handkiewicz-Junak, D.; Grana, C.; Mazzetta, C.; Rocca, P.; Bartolomei, M.; Lopera-Sierra, M.; Cremonesi, M.; Chinol, M.; Macke, H.R.; et al. Receptor radionuclide therapy with 90Y-DOTATOC in patients with medullary thyroid carcinomas. Cancer Biother. Radiopharm. 2004, 19, 65–71. [Google Scholar] [CrossRef] [PubMed]
  17. Iten, F.; Muller, B.; Schindler, C.; Rasch, H.; Rochlitz, C.; Oertli, D.; Maecke, H.R.; Muller-Brand, J.; Walter, M.A. ((90)Yttrium-DOTA)-TOC response is associated with survival benefit in iodine-refractory thyroid cancer long-term results of a phase 2 clinical trial. Cancer 2009, 115, 2052–2062. [Google Scholar] [CrossRef] [PubMed]
  18. Teunissen, J.J.M.; Kwekkeboom, D.J.; Kooij, P.P.M.; Bakker, W.H.; Krenning, E.P. Peptide receptor radionuclide therapy for non-radioiodine-avid differentiated thyroid carcinoma. J. Nucl. Med. 2005, 46, 107s–114s. [Google Scholar] [PubMed]
  19. Sundin, A.; Vullierme, M.P.; Kaltsas, G.; Plockinger, U.; Mallorca Consensus Conference Participants; European Neuroendocrine Tumor Society. Enets consensus guidelines for the standards of care in neuroendocrine tumors: Radiological examinations. Neuroendocrinology 2009, 90, 167–183. [Google Scholar] [CrossRef] [PubMed]
  20. Bombardieri, E.; Ambrosini, V.; Aktolun, C.; Baum, R.P.; Bishof-Delaloye, A.; del Vecchio, S.; Maffioli, L.; Mortelmans, L.; Oyen, W.; Pepe, G.; et al. 111In-pentetreotide scintigraphy: Procedure guidelines for tumour imaging. Eur. J. Nucl. Med. Mol. Imaging 2010, 37, 1441–1448. [Google Scholar] [CrossRef] [PubMed]
  21. Buchmann, I.; Henze, M.; Engelbrecht, S.; Eisenhut, M.; Runz, A.; Schafer, M.; Schilling, T.; Haufe, S.; Herrmann, T.; Haberkorn, U. Comparison of 68Ga-DOTATOC PET and 111In-DTPAOC (octreoscan) spect in patients with neuroendocrine tumours. Eur. J. Nucl. Med. Mol. Imaging 2007, 34, 1617–1626. [Google Scholar] [CrossRef] [PubMed]
  22. Bodei, L.; Cremonesi, M.; Ferrari, M.; Pacifici, M.; Grana, C.M.; Bartolomei, M.; Baio, S.M.; Sansovini, M.; Paganelli, G. Long-term evaluation of renal toxicity after peptide receptor radionuclide therapy with 90Y-DOTATOC and 177Lu-DOTATATE: The role of associated risk factors. Eur. J. Nucl. Med. Mol. Imaging 2008, 35, 1847–1856. [Google Scholar] [CrossRef] [PubMed]
  23. Valkema, R.; Pauwels, S.A.; Kvols, L.K.; Kwekkeboom, D.J.; Jamar, F.; de Jong, M.; Barone, R.; Walrand, S.; Kooij, P.P.; Bakker, W.H.; et al. Long-term follow-up of renal function after peptide receptor radiation therapy with (90)Y-DOTA(0), Tyr(3)-octreotide and (177)Lu-DOTA(0), Tyr(3)-octreotate. J. Nucl. Med. 2005, 46 (Suppl. 1), 83S–91S. [Google Scholar] [PubMed]
  24. Ljungberg, M.; Sjogreen-Gleisner, K. The accuracy of absorbed dose estimates in tumours determined by quantitative spect: A monte carlo study. Acta Oncol. 2011, 50, 981–989. [Google Scholar] [CrossRef] [PubMed]
  25. Konijnenberg, M.; Melis, M.; Valkema, R.; Krenning, E.; de Jong, M. Radiation dose distribution in human kidneys by octreotides in peptide receptor radionuclide therapy. J. Nucl. Med. 2007, 48, 134–142. [Google Scholar] [PubMed]
  26. Sgouros, G.; Hobbs, R.F. Dosimetry for radiopharmaceutical therapy. Semin. Nucl. Med. 2014, 44, 172–178. [Google Scholar] [CrossRef] [PubMed]
  27. Sjogreen, K.; Ljungberg, M.; Wingardh, K.; Minarik, D.; Strand, S.E. The lundadose method for planar image activity quantification and absorbed-dose assessment in radionuclide therapy. Cancer Biother. Radiopharm. 2005, 20, 92–97. [Google Scholar] [CrossRef] [PubMed]
  28. Siegel, J.A.; Thomas, S.R.; Stubbs, J.B.; Stabin, M.G.; Hays, M.T.; Koral, K.F.; Robertson, J.S.; Howell, R.W.; Wessels, B.W.; Fisher, D.R.; et al. Mird pamphlet No. 16: Techniques for quantitative radiopharmaceutical biodistribution data acquisition and analysis for use in human radiation dose estimates. J. Nucl. Med. 1999, 40, 37S–61S. [Google Scholar] [PubMed]
  29. Foster, D.M. Developing and testing integrated multicompartment models to describe a single-input multiple-output study using the saam II software system. Adv. Exp. Med. Biol. 1998, 445, 59–78. [Google Scholar] [PubMed]
  30. Bouchet, L.G.; Bolch, W.E.; Blanco, H.P.; Wessels, B.W.; Siegel, J.A.; Rajon, D.A.; Clairand, I.; Sgouros, G. Mird pamphlet No 19: Absorbed fractions and radionuclide S values for six age-dependent multiregion models of the kidney. J. Nucl. Med. 2003, 44, 1113–1147. [Google Scholar] [PubMed]
  31. Rolleman, E.J.; Valkema, R.; de Jong, M.; Kooij, P.P.; Krenning, E.P. Safe and effective inhibition of renal uptake of radiolabelled octreotide by a combination of lysine and arginine. Eur. J. Nucl. Med. Mol. Imaging 2003, 30, 9–15. [Google Scholar] [CrossRef] [PubMed]
  32. Lapa, C.; Werner, R.A.; Bluemel, C.; Lueckerath, K.; Muegge, D.O.; Strate, A.; Haenscheid, H.; Schirbel, A.; Allen-Auerbach, M.S.; Bundschuh, R.A.; et al. Prediction of clinically relevant hyperkalemia in patients treated with peptide receptor radionuclide therapy. EJNMMI Res. 2014, 4. [Google Scholar] [CrossRef] [PubMed]
  33. De Keizer, B.; van Aken, M.O.; Feelders, R.A.; de Herder, W.W.; Kam, B.L.; van Essen, M.; Krenning, E.P.; Kwekkeboom, D.J. Hormonal crises following receptor radionuclide therapy with the radiolabeled somatostatin analogue (177Lu-DOTA0,Tyr3)octreotate. Eur. J. Nucl. Med. Mol. Imaging 2008, 35, 749–755. [Google Scholar] [CrossRef] [PubMed]
  34. Melis, M.; Valkema, R.; Krenning, E.P.; de Jong, M. Reduction of renal uptake of radiolabeled octreotate by amifostine coadministration. J. Nucl. Med. 2012, 53, 749–753. [Google Scholar] [CrossRef] [PubMed]
  35. Ahlstedt, J.; Tran, T.A.; Strand, F.; Holmqvist, B.; Strand, S.E.; Gram, M.; Åkerström, B. Biodistribution and pharmacokinetics of recombinant α1-microglobulin and its potential use in radioprotection of kidneys. Am. J. Nucl. Med. Mol. Imaging 2015, 5, 333–347. [Google Scholar] [PubMed]
  36. Halliwell, B.; Gutteridge, J.M. The definition and measurement of antioxidants in biological systems. Free Radic. Biol. Med. 1995, 18, 125–126. [Google Scholar] [CrossRef]
  37. Buehler, P.W.; D’Agnillo, F. Toxicological consequences of extracellular hemoglobin: Biochemical and physiological perspectives. Antioxid. Redox Signal. 2010, 12, 275–291. [Google Scholar] [CrossRef] [PubMed]
  38. Fukai, T.; Ushio-Fukai, M. Superoxide dismutases: Role in redox signaling, vascular function, and diseases. Antioxid. Redox Signal. 2011, 15, 1583–1606. [Google Scholar] [CrossRef] [PubMed]
  39. Lubos, E.; Loscalzo, J.; Handy, D.E. Glutathione peroxidase-1 in health and disease: From molecular mechanisms to therapeutic opportunities. Antioxid. Redox Signal. 2011, 15, 1957–1997. [Google Scholar] [CrossRef] [PubMed]
  40. Goyal, M.M.; Basak, A. Human catalase: Looking for complete identity. Protein Cell 2010, 1, 888–897. [Google Scholar] [CrossRef] [PubMed]
  41. Ascenzi, P.; Bocedi, A.; Visca, P.; Altruda, F.; Tolosano, E.; Beringhelli, T.; Fasano, M. Hemoglobin and heme scavenging. IUBMB Life 2005, 57, 749–759. [Google Scholar] [CrossRef] [PubMed]
  42. Tenhunen, R.; Marver, H.S.; Schmid, R. The enzymatic conversion of heme to bilirubin by microsomal heme oxygenase. Proc. Natl. Acad. Sci. USA 1968, 61, 748–755. [Google Scholar] [CrossRef] [PubMed]
  43. Azzam, E.I.; de Toledo, S.M.; Little, J.B. Oxidative metabolism, gap junctions and the ionizing radiation-induced bystander effect. Oncogene 2003, 22, 7050–7057. [Google Scholar] [CrossRef] [PubMed]
  44. Lyng, F.M.; Seymour, C.B.; Mothersill, C. Production of a signal by irradiated cells which leads to a response in unirradiated cells characteristic of initiation of apoptosis. Br. J. Cancer 2000, 83, 1223–1230. [Google Scholar] [CrossRef] [PubMed]
  45. Lyng, F.M.; Seymour, C.B.; Mothersill, C. Initiation of apoptosis in cells exposed to medium from the progeny of irradiated cells: A possible mechanism for bystander-induced genomic instability? Radiat. Res. 2002, 157, 365–370. [Google Scholar] [CrossRef]
  46. Ekström, B.; Berggård, I. Human α1-microglobulin. Purification procedure, chemical and physiochemical properties. J. Biol. Chem. 1977, 252, 8048–8057. [Google Scholar] [PubMed]
  47. Åkerström, B.; Gram, M. A1M, an extravascular tissue cleaning and housekeeping protein. Free Radic. Biol. Med. 2014, 74, 274–282. [Google Scholar] [CrossRef] [PubMed]
  48. Flower, D.R. The lipocalin protein family: Structure and function. Biochem.J. 1996, 318, 1–14. [Google Scholar] [CrossRef] [PubMed]
  49. Åkerström, B.; Lögdberg, L. An intriguing member of the lipocalin protein family: α1-Microglobulin. Trends Biochem. Sci. 1990, 15, 240–243. [Google Scholar] [CrossRef]
  50. Breustedt, D.A.; Schonfeld, D.L.; Skerra, A. Comparative ligand-binding analysis of ten human lipocalins. Biochim. Biophys. Acta 2006, 1764, 161–173. [Google Scholar] [CrossRef] [PubMed]
  51. Meining, W.; Skerra, A. The crystal structure of human α1-microglobulin reveals a potential haem-binding site. Biochem. J. 2012, 445, 175–182. [Google Scholar] [CrossRef] [PubMed]
  52. Tejler, L.; Eriksson, S.; Grubb, A.; Astedt, B. Production of protein HC by human fetal liver explants. Biochim. Biophys. Acta 1978, 542, 506–514. [Google Scholar] [CrossRef]
  53. Kaumeyer, J.F.; Polazzi, J.O.; Kotick, M.P. The mRNA for a proteinase inhibitor related to the HI-30 domain of inter-α-trypsin inhibitor also encodes α-1-microglobulin (protein HC). Nucleic Acids Res. 1986, 14, 7839–7850. [Google Scholar] [CrossRef] [PubMed]
  54. Lindqvist, A.; Bratt, T.; Altieri, M.; Kastern, W.; Åkerström, B. Rat α1-microglobulin: Co-expression in liver with the light chain of inter-α-trypsin inhibitor. Biochim. Biophys. Acta 1992, 1130, 63–67. [Google Scholar] [CrossRef]
  55. Fries, E.; Blom, A.M. Bikunin—Not just a plasma proteinase inhibitor. Int. J. Biochem. Cell Biol. 2000, 32, 125–137. [Google Scholar] [CrossRef]
  56. Larsson, J.; Wingårdh, K.; Berggård, T.; Davies, J.R.; Lögdberg, L.; Strand, S.E.; Åkerström, B. Distribution of iodine 125-labeled α1-microglobulin in rats after intravenous injection. J. Lab. Clin. Med. 2001, 137, 165–175. [Google Scholar] [CrossRef] [PubMed]
  57. DeMars, D.D.; Katzmann, J.A.; Kimlinger, T.K.; Calore, J.D.; Tracy, R.P. Simultaneous measurement of total and IGA-conjugated α1-microglobulin by a combined immunoenzyme/immunoradiometric assay technique. Clin. Chem. 1989, 35, 766–772. [Google Scholar] [PubMed]
  58. Berggård, T.; Thelin, N.; Falkenberg, C.; Enghild, J.J.; Åkerström, B. Prothrombin, albumin and immunoglobulin a form covalent complexes with α1-microglobulin in human plasma. Eur. J. Biochem. FEBS 1997, 245, 676–683. [Google Scholar] [CrossRef]
  59. Nordberg, J.; Allhorn, M.; Winqvist, I.; Åkerström, B.; Olsson, M.L. Quantitative and qualitative evaluation of plasma and urine α1-microglobulin in healthy donors and patients with different haemolytic disorders and haemochromatosis. Clin. Chim. Acta Int. J. Clin. Chem. 2007, 386, 31–37. [Google Scholar] [CrossRef] [PubMed]
  60. Allhorn, M.; Berggård, T.; Nordberg, J.; Olsson, M.L.; Åkerström, B. Processing of the lipocalin α1-microglobulin by hemoglobin induces heme-binding and heme-degradation properties. Blood 2002, 99, 1894–1901. [Google Scholar] [CrossRef] [PubMed]
  61. Siebel, J.F.; Kosinsky, R.L.; Åkerström, B.; Knipp, M. Insertion of heme b into the structure of the cys34-carbamidomethylated human lipocalin α1-microglobulin: Formation of a ((heme)21-microglobulin))3 complex. ChemBioChem 2012, 13, 879–887. [Google Scholar] [CrossRef] [PubMed]
  62. Allhorn, M.; Klapyta, A.; Åkerström, B. Redox properties of the lipocalin α1-microglobulin: Reduction of cytochrome c, hemoglobin, and free iron. Free Radic. Biol. Med. 2005, 38, 557–567. [Google Scholar] [CrossRef] [PubMed]
  63. Olsson, M.G.; Olofsson, T.; Tapper, H.; Åkerström, B. The lipocalin α1-microglobulin protects erythroid K562 cells against oxidative damage induced by heme and reactive oxygen species. Free Radic. Res. 2008, 42, 725–736. [Google Scholar] [CrossRef] [PubMed]
  64. Rutardottir, S.; Nilsson, E.J.; Pallon, J.; Gram, M.; Åkerström, B. The cysteine 34 residue of A1M/α1-microglobulin is essential for protection of irradiated cell cultures and reduction of carbonyl groups. Free Radic. Res. 2013, 47, 541–550. [Google Scholar] [CrossRef] [PubMed]
  65. Åkerström, B.; Maghzal, G.J.; Winterbourn, C.C.; Kettle, A.J. The lipocalin α1-microglobulin has radical scavenging activity. J. Biol. Chem. 2007, 282, 31493–31503. [Google Scholar] [CrossRef] [PubMed]
  66. Berggård, T.; Cohen, A.; Persson, P.; Lindqvist, A.; Cedervall, T.; Silow, M.; Thogersen, I.B.; Jönsson, J.A.; Enghild, J.J.; Åkerström, B. α1-Microglobulin chromophores are located to three lysine residues semiburied in the lipocalin pocket and associated with a novel lipophilic compound. Protein Sci. 1999, 8, 2611–2620. [Google Scholar] [CrossRef] [PubMed]
  67. Sala, A.; Campagnoli, M.; Perani, E.; Romano, A.; Labo, S.; Monzani, E.; Minchiotti, L.; Galliano, M. Human α1-microglobulin is covalently bound to kynurenine-derived chromophores. J. Biol. Chem. 2004, 279, 51033–51041. [Google Scholar] [CrossRef] [PubMed]
  68. May, K.; Rosenlöf, L.; Olsson, M.G.; Centlow, M.; Mörgelin, M.; Larsson, I.; Cederlund, M.; Rutardottir, S.; Siegmund, W.; Schneider, H.; et al. Perfusion of human placenta with hemoglobin introduces preeclampsia-like injuries that are prevented by α1-microglobulin. Placenta 2011, 32, 323–332. [Google Scholar] [CrossRef] [PubMed]
  69. Olsson, M.G.; Allhorn, M.; Larsson, J.; Cederlund, M.; Lundqvist, K.; Schmidtchen, A.; Sorensen, O.E.; Mörgelin, M.; Åkerström, B. Up-regulation of A1M/α1-microglobulin in skin by heme and reactive oxygen species gives protection from oxidative damage. PLoS ONE 2011, 6, e27505. [Google Scholar] [CrossRef] [PubMed]
  70. Olsson, M.G.; Rosenlöf, L.W.; Kotarsky, H.; Olofsson, T.; Leanderson, T.; Mörgelin, M.; Fellman, V.; Åkerström, B. The radical-binding lipocalin A1M binds to a complex I subunit and protects mitochondrial structure and function. Antioxid. Redox Signal. 2013, 18, 2017–2028. [Google Scholar] [CrossRef] [PubMed]
  71. Olsson, M.G.; Allhorn, M.; Olofsson, T.; Åkerström, B. Up-regulation of α1-microglobulin by hemoglobin and reactive oxygen species in hepatoma and blood cell lines. Free Radic.Biol. Med. 2007, 42, 842–851. [Google Scholar] [CrossRef] [PubMed]
  72. Olsson, M.G.; Centlow, M.; Rutardottir, S.; Stenfors, I.; Larsson, J.; Hosseini-Maaf, B.; Olsson, M.L.; Hansson, S.R.; Åkerström, B. Increased levels of cell-free hemoglobin, oxidation markers, and the antioxidative heme scavenger α1-microglobulin in preeclampsia. Free Radic. Biol. Med. 2010, 48, 284–291. [Google Scholar] [CrossRef] [PubMed]
  73. Wester-Rosenlöf, L.; Casslen, V.; Axelsson, J.; Edström-Hägerwall, A.; Gram, M.; Holmqvist, M.; Johansson, M.E.; Larsson, I.; Ley, D.; Marsal, K.; et al. A1M/α1-microglobulin protects from heme-induced placental and renal damage in a pregnant sheep model of preeclampsia. PLoS ONE 2014, 9, e86353. [Google Scholar] [CrossRef] [PubMed]
  74. Nääv, A.; Erlandsson, L.; Axelsson, J.; Larsson, I.; Johansson, M.; Wester-Rosenlöf, L.; Mörgelin, M.; Casslen, V.; Gram, M.; Åkerström, B.; et al. A1M ameliorates preeclampsia-like symptoms in placenta and kidney induced by cell-free fetal hemoglobin in rabbit. PLoS ONE 2015, 10, e0125499. [Google Scholar] [CrossRef] [PubMed]
  75. Sverrisson, K.; Axelsson, J.; Rippe, A.; Gram, M.; Åkerström, B.; Hansson, S.R.; Rippe, B. Extracellular fetal hemoglobin induces increases in glomerular permeability: Inhibition with α1-microglobulin and tempol. Am. J. Physiol. Ren. Physiol. 2014, 306, F442–F448. [Google Scholar] [CrossRef] [PubMed]
  76. Olsson, M.G.; Nilsson, E.J.; Rutardottir, S.; Paczesny, J.; Pallon, J.; Åkerström, B. Bystander cell death and stress response is inhibited by the radical scavenger α1-microglobulin in irradiated cell cultures. Radiat. Res. 2010, 174, 590–600. [Google Scholar] [CrossRef] [PubMed]

Share and Cite

MDPI and ACS Style

Ahlstedt, J.; Tran, T.A.; Strand, S.-E.; Gram, M.; Åkerström, B. Human Anti-Oxidation Protein A1M—A Potential Kidney Protection Agent in Peptide Receptor Radionuclide Therapy. Int. J. Mol. Sci. 2015, 16, 30309-30320.

AMA Style

Ahlstedt J, Tran TA, Strand S-E, Gram M, Åkerström B. Human Anti-Oxidation Protein A1M—A Potential Kidney Protection Agent in Peptide Receptor Radionuclide Therapy. International Journal of Molecular Sciences. 2015; 16(12):30309-30320.

Chicago/Turabian Style

Ahlstedt, Jonas, Thuy A. Tran, Sven-Erik Strand, Magnus Gram, and Bo Åkerström. 2015. "Human Anti-Oxidation Protein A1M—A Potential Kidney Protection Agent in Peptide Receptor Radionuclide Therapy" International Journal of Molecular Sciences 16, no. 12: 30309-30320.

Article Metrics

Back to TopTop