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Review

Therapeutic Role of Alkaloids and Alkaloid Derivatives in Cancer Management

by
Kolawole Olofinsan
,
Heidi Abrahamse
and
Blassan P. George
*
Laser Research Centre, Faculty of Health Sciences, University of Johannesburg, P.O. Box 17011, Doornfontein 2028, South Africa
*
Author to whom correspondence should be addressed.
Molecules 2023, 28(14), 5578; https://doi.org/10.3390/molecules28145578
Submission received: 29 June 2023 / Revised: 14 July 2023 / Accepted: 20 July 2023 / Published: 22 July 2023
(This article belongs to the Special Issue New Anticancer Agents Based on Natural Products)
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Abstract

:
Cancer is a neoplastic disease that remains a global challenge with a reported prevalence that is increasing annually. Though existing drugs can be applied as single or combined therapies for managing this pathology, their concomitant adverse effects in human applications have led to the need to continually screen natural products for effective and alternative anticancer bioactive principles. Alkaloids are chemical molecules that, due to their structural diversity, constitute a reserve for the discovery of lead compounds with interesting pharmacological activities. Several in vitro studies and a few in vivo findings have documented various cytotoxic and antiproliferative properties of alkaloids. This review describes chaetocochin J, neopapillarine, coclaurine, reflexin A, 3,10-dibromofascaplysin and neferine, which belong to different alkaloid classes with antineoplastic properties and have been identified recently from plants. Despite their low solubility and bioavailability, plant-derived alkaloids have viable prospects as sources of viable lead antitumor agents. This potential can be achieved if more research on these chemical compounds is directed toward investigating ways of improving their delivery in an active form close to target cells, preferably with no effect on neighboring normal tissues.

Graphical Abstract

1. Introduction

Cancer is the common name given to a group of complex pathologies triggered by factors that damage genetic materials, thus resulting in uncontrolled cell proliferation and consequent formation of abnormal cells capable of attacking other near or distant cells [1]. While genetic alterations in normal tissues can also result in benign and premalignant tumors, there are indications that major health challenges associated with cancer diseases, especially those without an early diagnosis, are significantly linked to cancerous or malignant tumors [2]. According to Sung et al. [3], cancer is the principal cause of human mortality and a limitation to long life expectancy in many developed and developing countries. With about 19.3 million people affected in 2020, deaths due to this disease amounted to 10 million out of the former estimate. Moreover, by 2040, the worldwide health challenge due to cancer is projected to increase by 47%. Cancer has the possibility of developing in nearly any tissue or organ in the body. However, as of 2020, breast (2.26 million), lung (2.21 million), prostrate (1.41 million), skin (1.19 million) and colon (1.14 million) cancers represented the leading types of this pathology documented globally [3].
Currently, various clinically approved treatment modalities exist for cancer treatment. These include chemotherapy, radiotherapy, immunotherapy, hormone therapy and targeted therapy, which may be applied alone as monotherapy or together as a combined therapy. However, despite the success recorded with these therapeutic regimes, their application in cancer management is challenged by unwanted adverse effects, such as lack of specificity or toxicity with regard to normal cells, disease re-emergence years after treatment and poor bioavailability, amongst others [4,5]. Consequently, these factors, combined with the high cost of conventional cancer therapies, have led many people, especially those in developing countries, to explore pharmacologically active chemical compounds present in plant products as alternative treatment options [6].
Plants have been described as reservoirs of bioactive compounds for cancer treatment [7]. Newman and Cragg [8] revealed that about 35% of all anticancer drugs available for cancer management between 1981 and 2014 were obtained from plant products. Alkaloids represent one of the highly diverse categories of chemical compounds in plants that regulate plant growth and protect them against herbivory [9]. They have structural diversity, which results in them possessing various pharmacological properties, including anticancer effects. While alkaloids such as vinblastine first identified from plants are now clinically approved for cancer treatment, poor solubility, low bioavailability, drug resistance and hepatic toxicity have limited experiments with some alkaloids from advancing beyond in vitro and in vivo experiments. Consequently, this article first summarizes the significance and the mode of action of various classes of new plant anticancer drugs identified between 2019 and 2022 using PubMed and the Google Scholar database. It also proposes some ways of mitigating the poor pharmacokinetic properties associated with newly identified plant-derived alkaloids.

2. Alkaloids and Their General Applications

Alkaloids are organic chemical compounds with a cyclic ring structure containing one or more basic nitrogen atoms. They are widely distributed in nature and are found as naturally occurring secondary metabolites in both plants and animals. Despite this distribution, screening, identification and discovery of pharmacologically relevant alkaloids with usefulness in disease management have been carried out mainly with those chemical candidates derived from plant sources [10]. While they are primarily synthesized from amino acids, alkaloids can be found in seeds, roots, stems and leaves of higher plants, such as those in the Solanaceae, Ranunculaceae, Loganiaceae, Menispermaceae, Amaryllidaceae and Papaveraceae families [11]. Although alkaloids’ function in plants is complex and not fully understood, there are indications that their production in plants could be attributed to defensive evolution against biotic factors, such as pathogens, insects and animals, that could pose threats to their existence as hosts. Chen et al. [12] showed that 7-demethoxytylophorine, a phenanthroindolizidine alkaloid, has antifungal properties, with a minimum inhibitory concentration of 1.56 µg mL−1 against Penicillium italicum, which is responsible for blue mold disease in plants [13]. Moreover, Hikal et al. [14] reviewed the insecticidal activities of quinolone, pyridine and piperidine alkaloids against pests affecting various different plants.
According to Heinrich et al. (2021), alkaloids possess some unique chemical characteristics that make them interesting candidates for use in medicine. In their basic state, they are soluble under acidic conditions, whereas they become lipid membrane-permeable when neutral after losing their protons. With these properties, alkaloids have been used in various applications in plant and human disease treatments (Figure 1). Currently, morphine and its chemical derivative codeine, obtained from Papaver somniferu, are often used as analgesics. Before replacement with other effective plant-derived drugs (e.g., artemisine), the antimalarial properties of quinine were well explored following the 17th century [15]. Tubocurarine and ergonovine, from claviceps and ephedra plant species, respectively, have been used to suppress bleeding due their effects in narrowing blood vessels. Alkaloids, including ephedrine and atropine, have been administered to treat respiratory illnesses, while others, such as vincristine, berberine and vinblastine, have been employed as anticancer agents [9].

3. Alkaloids in Cancer Treatment: A Historical Perspective

The first type of alkaloid that was applied in cancer therapy was discovered in the 1950s accidentally from Vinca rosea, a plant that is also referred to as Catharanthus roseus, by two researchers; namely, Charles Beer and Robert Noble [16]. Knowledge of the traditional use of this plant in reducing blood glucose led them to investigate its hypoglycemic effect in rats. However, instead of these antihyperglycemic properties, they discovered a considerable reduction in bone marrow damage in these animals with a simultaneous decrease in blood leucocytes and granulocytes [17]. After this finding, more focused studies on rats with lymphocytic leukemia led to the characterization of vinblastine as the first clinical anticancer use of Vinca alkaloids. To date, many other chemical compounds of the same plant category, including colchicine, vinflunine, vincamine, vinorelbine and vincristine, have also been documented for their antitumor efficacies [18,19].

4. Chemistry of Anticancer Alkaloids

Alkaloids are a very diverse group of plant secondary metabolites. There is no uniform pattern of classifying them due to their structural variation, as observed in Figure 2, which often does not correlate with their biological activities. For instance, alkaloids with similar ring structures but synthesized from different metabolic pathways could possess different pharmacological activities [20]. Consequently, alkaloids can be classified depending on the type of plant families they are derived from. Typical examples of this taxonomical classification include vinblastine, present in Vinca rosea, an alkaloid from the plant family Apocyanaeae; lobeline, found in Lobelia inflata as derived from the Lobeliaceae family; and physostigmine, present in Physostigma venenosum as derived from the family Leguminosae [21].
Another form of alkaloid classification is based on the precursor biomolecule used as the starting material for their biosynthetic pathways. Under this classification, alkaloids produced from the same amino acids, like arginine, tyrosine, proline, tryptophan, lysine and aspartate, can all be grouped in a class despite possessing different pharmacological activities and taxonomic distributions [22]. However, according to Dey et al. [20], the best all-inclusive classification of these basic nitrogen-containing phytochemicals involves categorizing them based on their chemical structures into tropane, pyrrolizidine, piperidine, quinoline, isoquinoline, indole, steroidal, imidazole, purine and pyrrolidine alkaloids. Although this article does not discuss all alkaloids in relation to their known biological activities, it aims to cover available information concerning anticarcinogenic drug discovery by focusing on plant-derived alkaloids documented between 2019 and 2022 as having antineoplastic properties and their mode of action.

5. Anticancer Alkaloids from Plants

Screening of plants for pharmacologically active secondary metabolites is an ongoing process. Therefore, previously specified anticancer alkaloids identified from various plant species over 4 years are highlighted in Table 1. While these plant-derived alkaloids are discussed based on their different structural classes in the following sections, Figure 3 summarizes the various tissue targets for therapy from the positive outcomes of their in vitro anticancer experiments.

5.1. Proto-Alkaloids

Although alkaloids generally are described as having a basic nitrogen atom in a heterocyclic ring structure, some of these plant metabolites, known as proto-alkaloids, have nitrogen emanating from amino acid residues that is not present in different cyclic skeleton systems. They are simple alkaloids that constitute a small proportion of alkaloid phytochemicals and are often derived chemically from tryptophan, tyrosine or phenylalanine amino acids with aromatic side chains. Colchicine is a proto-alkaloid isolated from the Colchicum plant species. As a therapeutic drug, the use of colchine has been reported in the treatment of inflammatory pathologies [63]. Other studies carried out with the chemical derived from plant material suggest that it has a role in mitigating the progression of cancer diseases. According to Adham Foumani et al. [39], colchine isolated from Colchicum autumnale initiated apoptosis in human and mouse breast cancer cells by enhancing the cellular expression of selected caspases, tumor protein 53 (p53) and B-cell lymphoma 2-like protein 4 (Bax). The antiproliferative effect of Colchicum pusillum extract in colon cancer cells was associated with the alkaloid downregulation of the β-catenin-mediated signaling cascade [37]. Moreover, in another study, Sun et al. [38] indicated that treatment with 250–650 μM colchine led to oral cancer cell death via a mechanism that involved a considerable increase in cytosolic Ca2+ concentration due to signaling molecule release from the endoplasmic reticulum by phospholipase C activation.

5.2. Cumarine–Alkaloid Conjugate

Courmarin is a benzopyrone phenolic compound present naturally in many plant materials. While coumarin is vital to life processes such as photosynthesis, hormone regulation and respiration in plants, there are indications that coumarin derivatives discovered in some plant species have useful pharmacological properties. Amongst these coumarin conjugates that have been documented to have anticancer capacities is the alkaloid coumarin derivative compound neopapillarine found in the Neocryptodiscus papillaris plant of the family Apiaceae [50]. Investigations revealed that the coumarin alkaloid showed a preferential cytotoxic effect on renal cancer cell lines (UO31 and A498). Although this phytochemical was identified for the first time in this study, there is a need to carry out further research on this compound to unravel its cytotoxic mode of action in tumor cells.

5.3. Indole Alkaloids

Alkaloids with indole chemical structures constitute the largest category of alkaloid compounds. These indole parent chemical compounds contain one pentacyclic ring and a pyrrole five-membered ring with a basic nitrogen atom, reported to confer biological activity in this class of alkaloids [64]. The indole alkaloids are widely distributed among different plant families. Interestingly, clinically approved antitumor chemotherapeutic drugs, such as vinblastine and its chemical analogue vincristine, are classified as indole alkaloids. Recently, alkaloids with indole molecular structures and anticancer potential have been isolated from some plants. Fadaeinasab et al. [54] identified a new indole alkaloid called reflexin A and two other known ones from the bark of Rauvolfia reflexa. In vitro analysis showed that the compound invokes both early- and late-stage apoptosis in colon cancer cells. According to the authors, the early-stage apoptosis that happened in the cells was associated with caspase 9 induction, whereas the late-stage events that occurred after 48 h were linked with caspase 8 activation. Similar caspase-mediated apoptosis coupled with the inhibition of G1 phase DNA replication was reported in BEL-7402 and SMMC-7721 hepatocarcinoma cell lines treated with acetoxytabernosine alkaloid from Alstonia yunnanensis [30]. Another indole alkaloid identified as chaetocochin J was obtained from the fungus Chaetomium globosum of the plant family Chaetomiaceae. At an IC50 of around 0.5 μM, this compound inhibits the proliferation of SW480 and HCT116 colorectal carcinoma cells. Its anticancer ability was associated with the compound’s simultaneous elevation of the expression of phosphorylated AMP-activated protein kinase (AMPK), downregulation of phosphoinositide-3-kinase (PIK3R4) and formation of autophagolysosomes. These processes ultimately contributed to apoptosis and autophagy in the cancer cells after treatment with the compound. In the study by Dini et al. [33], another indole alkaloid, caulerpin, was isolated in addition to a phytosterol from a hexane extract of Halimeda cylindracea microalga collected from an Indonesian coral island. After this compound was eluted from a silica gel-packed column with n-hexane: ethanol solvent (8:2), the purified caulerpin was tested against NCL-H460 lung cancer cells. The results indicated that the compound demonstrated cytotoxic properties with an IC50 value of about 20.05 μg/mL.
Furthermore, investigations of caulerpin in HCT-116 and HT-29 colorectal cancer cells also suggested that the compound limited the cell migration and increased the apoptosis of the tumor cells [34]. Moreover, the insignificant toxicity of caulerpin displayed in human HDF and mouse NIH-3T3 normal fibroblast cell lines indicates its possible lesser adverse effect on normal cells if developed as an anticancer agent. In the study by Dyshlovoy et al. [25], 3,10-dibromofascaplysin, an indole alkaloid derivative, was reported to display an antiproliferative effect in 22rv1 drug-resistant prostate cancer cells. This bis-indole alkaloid, identified from Fascaplysinopsis reticulata, induced limited androgen receptor signaling and intensified the cells’ sensitivity to enzalutamide.

5.4. Quinoline Alkaloid Derivatives

The quinoline heterocyclic ring and its derivatives have been described as sources of chemical components with pharmacological usefulness in organic and medicinal chemistry [65]. More importantly, their structural scaffold has been reported as a chemical assembly for developing anticancer entities [66,67]. Quinoline is a benzopyridine organic molecule that structurally has a benzene ring fused with a nitrogen-containing pyrimidine ring. It is from this basic skeleton that various related phytochemicals are formed. Compounds with similar quinoline structures derived from plants, as presented in Table 1, include isoquinoline, benzylisoquinoline and aporphine alkaloids. While the benzylisoquinoline alkaloids are structurally related to the isoquinoline alkaloids but with a benzyl group attached to C1 of the latter, the ring system of aporphine alkaloids appears to be more complex since it has more than two fused heterocyclic structures. Despite their structural diversity, quinoline alkaloid derivatives obtained from different plant sources have been reported to show antineoplastic effects on various cancer cells. Al-Ghazzawi [29] identified two benzylisoquinolines (namely, coclaurine and 6, 7-dimethoxy-1-(α-hydroxy-4-methoxybenzyl)-2-methyl-1, 2, 3, 4-tetrahydroisoquinoline) from the sugar apple plant (Annona squamosa). The results obtained after testing these compounds against HCT116, MCF-7 and HEPG-2 human colon, breast and liver cancer cell lines, respectively, indicated their anticancer effects. Although the compounds had greater potency in the liver cell lines, the presence of more hydroxyl groups in coclaurine gave it superiority over the other compound. Neferine is another reported benzylisoquinoline alkaloid obtained from Nelumbo nucifera seed embryos [49]. The compound induced apoptosis in HeLa and SiHa cervical cancer cells by enhancing reactive oxygen species (ROS) generation while increasing the expression of cytochrome c and other apoptotic proteins. Palmatine and 6-methoxydihydroavicine isoquinoline alkaloids were isolated from Berberis cretica and Macleaya cordata, respectively [28,51]. Reports by Ma et al. [28] and Zhang et al. [27] suggest that 6-methoxydihydroavicine increased cellular ROS generation and interfered with mitochondria oxaloacetic acid metabolism during glycolysis in pancreatic and ovarian carcinoma cancer cells. In contrast, palmatine sensitizes MCF-7 cells to doxorubicin treatment by inhibiting the breast cancer estrogen receptors. However, the antiproliferative properties of the aporphine alkaloid crebanine N-oxide from Stephania hainanensis were due to G2/M phase cell cycle arrest and apoptosis by caspase 3 and cytochrome c protein expression [40].
Matada et al. [65] have also described the anticancer ability of the camptothecin pyrroloquinoline alkaloid, first identified from Camptotheca acuminata, a woody plant from China. To prevent excessive logging of this plant for the cytotoxic compound, other researchers have investigated the possibility of extracting this compound or its derivatives from endophytes cultured from the plant part. Interestingly, 10-hydroxycamptothecin, obtained from C. acuminata endophytic fungi (Xylaria sp.), has been revealed to inhibit bromodomain-containing protein 4 (BDR4) in MDA-MB-231 triple-negative breast cancer cells [31,68]. Moreover, camptothecin and its related chemicals have been reported to exert their antitumor activity by inhibiting topoisomerase 1 [32]. The complex formed when camptothecin binds to topoisomerase and DNA obstructs the movement of the replication fork and thus creates shear stress that leads to the death of the cell [32].

5.5. Carbazole Alkaloid

The carbazole alkaloid’s structural motif consists of a pyrrole ring with nitrogen fused at both sides by a benzene cyclic ring. This heterocyclic alkaloid class has been identified from metabolites from bacteria and plant sources. Although these alkaloids are found as natural products, their intriguing biological activities have stimulated synthetic chemists’ interest in producing them from inorganic molecules [69]. Most of the reported carbazole alkaloids found in plants have been documented in the Rutaceae family. One of the plants in this family from which several carbazole alkaloids have been characterized in the past few years is Murraya koenigii or the curry tree plant. Yang and Yu [45] discovered that girinimbine from this plant induced apoptosis in MDA-MB-453 breast cancer cells by inhibiting the mitogen-activated protein kinase/extracellular signal-regulated kinase (MEK/ERK) pathway, which is vital for cell survival. In another report, Satyavarapu et al. [46] isolated koenimbine, mahanimbine and mahanine from leaves of the same plant and investigated their antitumor activities against ovarian, lung and bladder cancer cell lines. In another report, mahanimbine and koenimbine lowered the metabolism of PC-3 prostate cancer and OVCAR3 ovarian cancer cells, while mahanine caused anoikis in the same cells via microtubule-associated protein (LC3) induction. This latter process, which resulted in autophagy coupled with a reduction in p62 protein expression, was described as one of the mechanisms involved in mahanimbine-mediated cell death in Hs172.T bladder cancer cells [47].
Carbazole alkaloids have also been identified in Glycosmis pentaphylla. This plant of the family Rutaceae, previously known as Glycosmis arborea, is common to the northwest regions of Australia and southern Asia, where it is cultivated for its edible fruit [70]. In the investigation by Ito et al. [23], glybomines and other carbazole alkaloid derivatives, such as 3-methoxyl carbazole, were discovered in the acetone extract of dried Glycosmis arborea stem. Moreover, in a recent experiment, the characterization of the carbazole isolated from Glycosmis pentaphylla stem ethanol extract indicated the presence of glycosmisines A and B [71]. These compounds suppressed the proliferation of liver hepG2 and A547 lung cancer cells in a concentration-dependent manner. Glycosmisine A’s IC50 values for these cell lines were 50.30 μM and 43.68 μM, whereas, for glycosmisine B, the IC50 values were 62.89 μM and 57.10 μM. Moreover, Alanazi et al. [24] also showed that 3 methoxy carbazole mediates MCF-7 breast cancer apoptotic cell death by elevating reactive oxygen species production and caspase 3 protein expression.
Besides the Glycosmis and Murraya species, several carbazole alkaloids with anticancer bioactivities have been reported in Clausena plant species [72]. Claulansines and claulamine carbazoles were isolated from Clausena lansiuma stem, while clauemarazoles were present in the same morphological part of Clausena emarginata [73,74]. Moreover, various clausenawalline alkaloids were found to be present in acetone extract from Clausena wallichii twigs [75]. Andas et al. [44] purified dentatin carbazole from Clausena excavate root extract. The mechanism studies in this work suggested that dentatin inhibited nuclear factor kappa B (NF-κB) and increased caspase 3 and 9 expressions in HepG2 cells. In another experiment, dentatin was reported to induce apoptosis in colorectal carcinoma cells by stimulating G0/G1 cell cycle arrest while elevating the protein level of Th1-type cytokines [43].

5.6. Indoloquinazoline Alkaloid

Quinazoline-containing organic compounds have been described as an important pharmacologically active class of therapeutic agents. Quinazolines have a structural variant of the quinoline skeletal architecture. However, the pyrimidine cyclic ring fused with the benzene in quinazoline contains two nitrogen atoms. Indoloquinazole alkaloids are quinazoline derivatives identified from some plant species that have been reported to possess cytotoxic properties against cancer cells. One of the plants from which indoloquinazoline alkaloids have been characterized is Araliopsis soyauxii. In the Noulala et al. [60] study, soyauxinine and other known phytocompounds were isolated from the stem bark of the flowering plant using the nuclear magnetic resonance and mass spectroscopy analytical techniques. Treatment of CCRF-CEM cells with the compound at 3.64 μM IC50 altered mitochondrial membrane potential and elevated ROS levels and apoptotic caspase protein expression in the leukemia cells. However, according to Noulala et al. [61], soyauxinine showed poor antiproliferative effects on colon HT-29 and prostate PC-3 cancer cells.

5.7. Steroidal Alkaloid

Structurally, steroidal alkaloids are chemical derivatives of plant steroids but with one or more nitrogen atoms in their heterocyclic rings. Due to their characteristic similarities with steroids, they have been described as having the biological properties of both alkaloids and steroids [76]. With no documented role in plant development and reproduction, steroidal alkaloids are associated with protection against environmental factors that threaten plant survival [76]. Steroidal alkaloids are found in various plant species growing in Africa’s tropical and sub-tropical regions. Despite this diverse distribution and their varied biological activities, according to Abd Karim et al. [77], their presence is limited to the Buxaceae, Liliaceae, Apocynaceae and Solanaceae plant families. Solamargine is a steroidal alkaloid isolated from some Solanaceae species. Interestingly, the anticancer bioactivity of this phytocompound has been evidenced in previous studies. Solamargine evokes cell death in castration-resistant prostate cancer cells by suppressing phosphorylated Akt expression, with consequent dysfunction of the PI3K/Akt signaling pathway [58]. The compound demonstrated its antitumor properties in gastric cancer cell lines by interfering with the MAPK signaling cascade through the suppression of the nuclear paraspeckle assembly transcript 1 (NEAT1) protein level [59]. Moreover, the same compound obtained from Solanum aculeastrum fruits at 15.62 μg/mL IC50 caused a 9.1-fold inhibition of P-glycoprotein in the SH-SY5Y neuroblastoma cell line. Among the Buxaceae family plants, Buxus sempervirens leaves and twigs have been reported to possess cyclovirobuxine D and imperialine steroid alkaloids [78]. The formal compound, according to Lu et al. [42], induces autophagy in breast cancer cells by enhancing autophagy-related ATG5 expression, converting autophagosome biomarker LC3 from type I to III and concomitantly suppressing the Akt/mTOR signaling pathway. Paravallarine is another sterol alkaloid with anticancer properties. In the experiment in [79], this alkaloid was obtained from Kibatalia laurifolia (Apocynaceae) leaves with some other compounds. Moreover, cyclopamine isolated from Veratrum californicum in the Liliaceae family was documented to induce apoptosis of cancerous breast cells through the distortion of Smo protein function by impeding Hedgehog signaling cascade [41,80]

5.8. Piperidine Alkaloid

Piperidine alkaloids have a piperidine heterocyclic chemical structure with one amide bond and five methylene linkages. Although piperidine alkaloids such as euphococcinine and pinidinone have been identified in insects, the majority of these alkaloids investigated for the use of their lead pharmacological properties in drug development are from plants [81]. More importantly, studies have described plant species in the Piperaceae family as rich sources of piperidine alkaloids [82]. One of these plants is Piper nigrum or black pepper, which has been described as a source of essential piperidine alkaloids, including piperidine and its substituted derivatives. Interestingly, these two compounds have been widely researched for their antitumor activities against different cancer cells [83,84]. Piperlongumine is another piperidine alkaloid isolated from Piper longum or Indian long pepper, which belongs to the Piperaceae plant family. Awasthee et al. [52] evaluated the anticancer effects of this alkaloid on different cancer cell lines (MCF-7, MDA-MB-468, T-47D, MDA-MB-231) as a single treatment and in combination with doxorubicin. The results showed that the alkaloid at 1–20 μM dose-dependently lowered glucose uptake by modulating glucose transporter-1 (GLUT-1) with concomitant elevation of monocarboxylate transporter 4 (MCT-4) expression in the breast tumor cells. Furthermore, the alkaloid at 20 μM potentiated doxorubicin-mediated cytotoxicity in the cell by 40%. In another experiment with a Balb/c mice in vivo model, piperlongumine suppressed Bcl-2 protein level and inhibited the G2/M phase of the cell cycle in colonocytes isolated from animals with 1,2-dimethylhydrazine/dextran sulphate sodium-induced colon carcinogenesis [53].
Piper methysticum is another Piperaceae reported to possess piperidine alkaloids. In Dragull et al.’s [85] study, two major piperidines, awaine and pipermethystine, were obtained from various parts of this plant. While the first was found in the young leaves, the second was more concentrated in the peels of the plant stems. Surprisingly, piperidine alkaloids have also been documented in plants that do not belong to Piperaceae. The report by Viegas et al. [86] described the isolation of four piperidine alkaloids from Cassia spectabilis of the Fabaceae plant family. These compounds included iso-6-spectaline, 7-hydroxyspectaline, spectaline and 3-O-acetylspectaline. While the authors found these alkaloids in the flowers, they discovered that the latter two were also present in the green fruits of the plant. Microcos paniculate (Malvaceae) leaves have also been reported to contain microcosamine A and C piperidine alkaloids [87]. Interestingly, studies by Still et al. [48] revealed that microcosamine A displayed antiproliferative effects in HT-29 colon cancer cells, acting as an antagonist of nicotinic acetylcholine receptors (α4β2 and α3β4).

6. Plant Alkaloids in Clinical Trials

Many anticancer alkaloids first identified from plant sources, such as vincristine and vinblastine, have passed rigorous drug screening tests, including human trials, prior to their approval by government agencies as clinical therapeutic drugs. Interestingly, knowledge of structure–activity relationships has also encouraged chemists to synthesize various analogs of these compounds to formulate better drugs with enhanced potency [88]. However, the associated toxicity linked with these synthetic antitumor products has resulted in the need to discover more phytoproducts with lower adverse effects for human disease management. Tilaoui et al. [89] described some clinical experimental work on some known plant-derived alkaloids in relation to cancer treatment. Amongst these anticancer alkaloids was homoharringtonine, obtained from the Cephalotaxus fortunei plant. Homoharringtonine, a protein synthesis inhibitor approved by the US Food and Drug Administration (FDA), resulted in a hematologic recovery rate of about 72% in patients with severe myeloid leukemia [90,91]. In a more recent randomized investigation with children (>2 years) with this same disease, the authors of [92] suggested that homoharringtonine resulted in a superior 88.0% ± 6.5 5-year event-free survival rate compared to 60.2% ± 9.6% in children managed with an anthracycline treatment regimen. Since P65 activation is involved in MYC gene overexpression in blood malignancies, homoharringtonine downregulates this process by causing P-65 to bond tightly with NF-κB repressing factor (NKRF) [93,94].
Although caffeine and its related plant-derived alkaloid theobromine are well known for their diverse pharmacological properties, their potential chemo-preventive effects in breast cancer have also been reported [95]. Before undergoing tumor operation, patients were fed capsules containing 19.7 mg caffeine/theobromine and a 473.7 mg mixture of 37 phenolic compounds. Analysis of malignant tissue metabolites showed the presence of theobromine amongst other compounds. Although methylxanthine did not exert a cytotoxic effect in MCF-7 breast cancer cells at the concentration at which it was detected in the malignant tissue, the authors suggested that the persistence of these metabolites despite fasting before surgery at a level comparable with normal subjects may necessitate a further clinical investigation of their long-term effect in cancer management.
Another plant alkaloid studied in human experiments in the last 5 years is berberine. In Chen et al.’s [96] study, this isoquinoline alkaloid was given twice daily (0.3 g) to 553 individuals aged 18–75 years who had undergone complete polypectomy after being verified to have colorectal adenoma. Six months after the patients’ surgery, treatment with berberine was carried out for 2 years before reoccurrence of colorectal adenomas in the subjects was evaluated. Besides complaints about slight constipation from the participants, the drug was found to prevent colorectal cancer reappearance at the experimental dose without any serious adverse effects.

7. Limitations of Alkaloids in Cancer Treatment

Despite the significant contributions of alkaloids and their various derivatives in cancer disease therapeutics, the complete adoption of these diverse biologically active nitrogen-containing heterocyclic compounds is still limited by several ongoing pharmacological challenges. One of these problems is the issue of bioavailability. Before a drug ingested or injected into the body can exert a therapeutic effect in its target tissue, it must penetrate the site in active form and at a specific effective concentration. However, alkaloids from plants generally have low bioavailability, which studies have associated with their low solubility in body fluids with poor cell membrane permeability [97]. To enhance alkaloids’ transport through the body’s aqueous system and their effective concentration at their intended site of action, Sindhoor et al. [98] suggested their inclusion in organic carriers, such as liposomes, dendrimers or polymer-based formulations. Liposome molecules such as phosphatidylcholine can hide hydrophobic chemical compounds in their core while exposing their hydrophilic end to the exterior in contact with polar body fluids. They can help transport alkaloid drugs through the blood to various target tissues in this form. Interestingly, the specificity of alkaloid-carrying liposomes can be enhanced by conjugating them with other components that can be identified by their proteins, such as folate receptors, which are highly expressed on the surfaces of many tumor cells. Previous findings have shown the anticancer efficacy of doxorubicin-liposome carrier increased significantly after surface functionalization with polyethylene glycol [99,100].
Chemotherapy is a major cancer treatment method but the success achieved using this procedure over time has been limited by the problem of drug resistance. Some cancer cells have devised ways of evading death from certain drug treatments by altering some endogenous protein isoforms, increasing the cellular expression of specific efflux proteins and repressing apoptotic event pathways [17]. These mechanisms, amongst other processes, were reported in a study of lung cancer cells’ resistance to Vinca alkaloid treatment [17]. The results of the reverse transcriptase polymerase chain reaction analysis carried out on tumor samples obtained from patients with non-small cell lung cancer revealed a considerable increase in p-glycoprotein expression during chemotherapy treatment, including vincristine and vinorelbine alkaloids [101]. Vinca alkaloids are substrates for p-glycoproteins [102]. Consequently, these phytocompounds’ efficacies can be enhanced by combining them with other chemotherapeutic drugs.
Regardless of the different antiviral, antidiabetic and antibacterial biological activities of some pyrrolizidine alkaloids [103], one of the main constraints that has prevented their screening for possible anticancer activities beyond in vitro and in vivo small animal experiments is their potential toxicity after metabolism in humans. Findings have shown that pyrrolizidine alkaloids in the liver are oxidized at C1 and C2 by the cytochrome P450 system to produce a dehydrogenated derivative with a pyrrole ring system after ingestion. This structure then spontaneously releases the oxygenated group linked to C7 and C9 of the core heterocyclic motif to produce a chemically active species capable of reacting with protein and genetic macromolecules [104]. Due to this genotoxic effect, pyrrolizidine alkaloids could provide an interesting source of lead antitumor compounds. However, their application in practical cancer therapy may not be realistic because of the adverse impact of their active metabolite on normal cells. Nevertheless, using a gold-based artificial metalloenzyme instead of the P450 liver enzyme as a catalyst, Kurimoto et al. [105], in their studies, described the conversion of a cyclized dehydrogenated pyrrolizidine precursor to an active form that produced significant cytotoxicity in HeLa, A549 and SW620 cancer cell lines. This experiment showed that, in the absence of liver metabolism, pyrrolizidine can be an effective anticancer agent without a negative effect on normal cells if artificially converted into its active form near the target tissue.

8. Conclusions

Due to changing lifestyles and increasing industrialization, the prevalence of cancer has been projected to rise in the coming years. Despite the effectiveness of the available treatments for this pathology, the adverse outcomes of existing anticancer drugs require a continuous search for alternative therapeutic chemicals, especially from plant sources. In this regard, phytochemicals of natural origin, collectively described as alkaloids, have proven to be viable sources of potent antitumor compounds. There is a need to discover more of these natural products, that which provide better activities with lower toxicities in relation to the presently approved synthetic anticancer drugs. While they may possess low solubility and bioavailability, more research should be carried out investigating the various delivery methods that can be employed to improve the solubility of the already identified plant-derived alkaloids while also determining ways of enhancing their other pharmacokinetic properties to enable practical application in cancer treatment. As most of the available studies on these plant alkaloids were undertaken in vitro, a better understanding of these compounds’ mechanism of action can be obtained if they are subject to in vivo investigations with small animals. These findings will allow researchers to identify more alkaloids that could advance in testing in pre-clinical and clinical studies.

Author Contributions

Conceptualization, K.O. and B.P.G.; writing—original draft preparation, K.O.; writing—review and editing, B.P.G. and H.A.; supervision, B.P.G. and H.A. All authors have read and agreed to the published version of the manuscript.

Funding

This work was based on research funded by the South African Research Chairs initiative of the Department of Science and Technology and the National Research Foundation (NRF) of South Africa (grant no. 98337) and the South African Medical Research Council (grant no. SAMRC EIP007/2021), as well as through grants received from the NRF Research Development Grants for Y-Rated Researchers (grant no. 137788), the University Research Committee (URC), the African Laser Centre (ALC), the University of Johannesburg and the Council for Scientific and Industrial Research (CSIR)—National Laser Centre (NLC).

Institutional Review Board Statement

Not appliable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

Authors declare no conflict of interest.

References

  1. Nia, H.T.; Munn, L.L.; Jain, R.K. Physical traits of cancer. Science 2020, 370, eaaz0868. [Google Scholar] [CrossRef] [PubMed]
  2. Patel, A. Benign vs Malignant Tumors. JAMA Oncol. 2020, 6, 1488. [Google Scholar] [CrossRef] [PubMed]
  3. Sung, H.; Ferlay, J.; Siegel, R.L.; Laversanne, M.; Soerjomataram, I.; Jemal, A.; Bray, F. Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries. CA Cancer J. Clin. 2021, 71, 209–249. [Google Scholar] [CrossRef]
  4. Amini, P.; Moazamiyanfar, R.; Dakkali, M.S.; Khani, A.; Jafarzadeh, E.; Mouludi, K.; Khodamoradi, E.; Johari, R.; Taeb, S.; Najafi, M. Resveratrol in Cancer Therapy: From Stimulation of Genomic Stability to Adjuvant Cancer Therapy: A Comprehensive Review. Curr. Top Med. Chem. 2022, 23, 629–648. [Google Scholar]
  5. Eisenmann, E.D.; Talebi, Z.; Sparreboom, A.; Baker, S.D. Boosting the oral bioavailability of anticancer drugs through intentional drug–drug interactions. Basic Clin. Pharmacol. Toxicol. 2022, 130, 23–35. [Google Scholar] [CrossRef] [PubMed]
  6. Sarbadhikary, P.; George, B.P. A Review on Traditionally Used African Medicinal Plant Annickia chlorantha, Its Phytochemistry, and Anticancer Potential. Plants 2022, 11, 2293. [Google Scholar] [CrossRef]
  7. Olawale, F.; Iwaloye, O.; Olofinsan, K.; Ogunyemi, O.M.; Gyebi, G.A.; Ibrahim, I.M. Homology modelling, vHTS, pharmacophore, molecular docking and molecular dynamics studies for the identification of natural compound-derived inhibitor of MRP3 in acute leukaemia treatment. Chem. Pap. 2022, 76, 3729–3757. [Google Scholar] [CrossRef]
  8. Newman, D.J.; Cragg, G.M. Natural products as sources of new drugs from 1981 to 2014. J. Nat. Prod. 2016, 79, 629–661. [Google Scholar] [CrossRef] [Green Version]
  9. Joanna, K. Introductory Chapter. In Alkaloids–Their Importance in Nature and for Human Life; Joanna, K., Ed.; IntechOpen: Rijeka, Croatioa, 2019. [Google Scholar]
  10. Heinrich, M.; Mah, J.; Amirkia, V. Alkaloids used as medicines: Structural phytochemistry meets biodiversity—An update and forward look. Molecules 2021, 26, 1836. [Google Scholar] [CrossRef]
  11. Debnath, B.; Singh, W.S.; Das, M.; Goswami, S.; Singh, M.K.; Maiti, D.; Manna, K. Role of plant alkaloids on human health: A review of biological activities. Mat. Today Chem. 2018, 9, 56–72. [Google Scholar] [CrossRef]
  12. Chen, C.; Qi, W.; Peng, X.; Chen, J.; Wan, C. Inhibitory effect of 7-demethoxytylophorine on Penicillium italicum and its possible mechanism. Microorganisms 2019, 7, 36. [Google Scholar] [CrossRef] [Green Version]
  13. Kanashiro, A.M.; Akiyama, D.Y.; Kupper, K.C.; Fill, T.P. Penicillium italicum: An underexplored postharvest pathogen. Front. Microbiol. 2020, 11, 606852. [Google Scholar] [CrossRef]
  14. Hikal, W.M.; Baeshen, R.S.; Said-Al Ahl, H.A. Botanical insecticide as simple extractives for pest control. Cogent Biol. 2017, 3, 1404274. [Google Scholar] [CrossRef]
  15. Shanks, G.D. Historical review: Problematic malaria prophylaxis with quinine. Am. J. Trop. Med. Hyg. 2016, 95, 269. [Google Scholar] [CrossRef] [PubMed]
  16. Banyal, A.; Tiwari, S.; Sharma, A.; Chanana, I.; Patel, S.K.S.; Kulshrestha, S.; Kumar, P. Vinca alkaloids as a potential cancer therapeutics: Recent update and future challenges. 3 Biotech 2023, 13, 211. [Google Scholar] [CrossRef] [PubMed]
  17. Zhang, Y.; Yang, S.H.; Guo, X.L. New insights into Vinca alkaloids resistance mechanism and circumvention in lung cancer. Biomed. Pharmacother. 2017, 96, 659–666. [Google Scholar] [CrossRef]
  18. Gerullis, H.; Wawroschek, F.; Köhne, C.-H.; Ecke, T.H. Vinflunine in the treatment of advanced urothelial cancer: Clinical evidence and experience. Ther. Adv. Urol. 2017, 9, 28–35. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  19. Dhyani, P.; Quispe, C.; Sharma, E.; Bahukhandi, A.; Sati, P.; Attri, D.C.; Szopa, A.; Sharifi-Rad, J.; Docea, A.O.; Mardare, I. Anticancer potential of alkaloids: A key emphasis to colchicine, vinblastine, vincristine, vindesine, vinorelbine and vincamine. Cancer Cell Int. 2022, 22, 206. [Google Scholar] [CrossRef] [PubMed]
  20. Dey, P.; Kundu, A.; Kumar, A.; Gupta, M.; Lee, B.M.; Bhakta, T.; Dash, S.; Kim, H.S. Analysis of alkaloids (indole alkaloids, isoquinoline alkaloids, tropane alkaloids). In Recent Advances in Natural Products Analysis; Elsevier: Amsterdam, The Netherlands, 2020; pp. 505–567. [Google Scholar]
  21. Singh, R. Chemotaxonomy: A tool for plant classification. J. Med. Plants Stud. 2016, 4, 90–93. [Google Scholar]
  22. Eguchi, R.; Ono, N.; Hirai Morita, A.; Katsuragi, T.; Nakamura, S.; Huang, M.; Amin, A.U.M.; Kanaya, S. Classification of alkaloids according to the starting substances of their biosynthetic pathways using graph convolutional neural networks. BMC Bioinform. 2019, 20, 380. [Google Scholar] [CrossRef] [Green Version]
  23. Lockhart, S.M.; O’Rahilly, S. Colchicine—An old dog with new tricks. Nat. Metb. 2021, 3, 451–452. [Google Scholar] [CrossRef]
  24. Adham Foumani, E.; Irani, S.; Shokoohinia, Y.; Mostafaie, A. Colchicine of Colchicum autumnale, A Traditional Anti-Inflammatory Medicine, Induces Apoptosis by Activation of Apoptotic Genes and Proteins Expression in Human Breast (MCF-7) and Mouse Breast (4T1) Cell Lines. Cell J. 2022, 24, 647–656. [Google Scholar] [PubMed]
  25. Ito, C.; Itoigawa, M.; Sato, A.; Hasan, C.M.; Rashid, M.A.; Tokuda, H.; Mukainaka, T.; Nishino, H.; Furukawa, H. Chemical Constituents of Glycosmis a rborea: Three New Carbazole Alkaloids and Their Biological Activity. J. Nat. Prod. 2004, 67, 1488–1491. [Google Scholar] [CrossRef] [PubMed]
  26. Alanazi, J.; Unnisa, A.; Alanazi, M.; Alharby, T.N.; Moin, A.; Rizvi, S.M.D.; Hussain, T.; Awadelkareem, A.M.; Elkhalifa, A.O.; Faiyaz, S.S.M. 3-Methoxy Carbazole Impedes the Growth of Human Breast Cancer Cells by Suppressing NF-κB Signaling Pathway. Pharmaceuticals 2022, 15, 1410. [Google Scholar] [CrossRef]
  27. Dyshlovoy, S.A.; Kaune, M.; Hauschild, J.; Kriegs, M.; Hoffer, K.; Busenbender, T.; Smirnova, P.A.; Zhidkov, M.E.; Poverennaya, E.V.; Oh-Hohenhorst, S.J. Efficacy and mechanism of action of marine alkaloid 3, 10-dibromofascaplysin in drug-resistant prostate cancer cells. Mar. Drugs 2020, 18, 609. [Google Scholar] [CrossRef] [PubMed]
  28. Zhidkov, M.E.; Kaune, M.; Kantemirov, A.V.; Smirnova, P.A.; Spirin, P.V.; Sidorova, M.A.; Stadnik, S.A.; Shyrokova, E.Y.; Kaluzhny, D.N.; Tryapkin, O.A. Study of Structure–Activity Relationships of the Marine Alkaloid Fascaplysin and Its Derivatives as Potent Anticancer Agents. Mar. Drugs 2022, 20, 185. [Google Scholar] [CrossRef] [PubMed]
  29. Zhang, H.; Shangguan, F.; Zhang, L.; Ma, N.; Song, S.; Ma, L.; Liu, C.; Liu, M.; An, J.; Li, H. A novel mechanism of 6-methoxydihydroavicine in suppressing ovarian carcinoma by disrupting mitochondrial homeostasis and triggering ROS/MAPK mediated apoptosis. Front Pharmacol. 2023, 14, 1093650. [Google Scholar] [CrossRef]
  30. Ma, N.; Shangguan, F.; Zhou, H.; Huang, H.; Lei, J.; An, J.; Jin, G.; Zhuang, W.; Zhou, S.; Wu, S. 6-methoxydihydroavicine, the alkaloid extracted from Macleaya cordata (Willd.) R. Br. (Papaveraceae), triggers RIPK1/Caspase-dependent cell death in pancreatic cancer cells through the disruption of oxaloacetic acid metabolism and accumulation of reactive oxygen species. Phytomedicine 2022, 102, 154164. [Google Scholar]
  31. Al-Ghazzawi, A.M. Anti-cancer activity of new benzyl isoquinoline alkaloid from Saudi plant Annona squamosa. BMC Chem. 2019, 13, 1–6. [Google Scholar] [CrossRef] [Green Version]
  32. Lai, Q.; Yang, C.J.; Zhuang, M.; Ma, Y.H.; Lin, C.Y.; Zeng, G.Z.; Yin, J.L. Alkaloid from Alstonia yunnanensis diels root against gastrointestinal cancer: Acetoxytabernosine inhibits apoptosis in hepatocellular carcinoma cells. Front. Pharmacol. 2022, 13, 1085309. [Google Scholar] [CrossRef]
  33. Si, P.; Chen, H.; Liu, J.; Zhang, E.; Li, C.; Gu, J.; Wang, R.; Li, W. Identification of (S)-10-Hydroxycamptothecin as a potent BRD4 inhibitor for treating triple-negative breast cancer. J. Mol. Struct. 2022, 1265, 133366. [Google Scholar] [CrossRef]
  34. Li, F.; Jiang, T.; Li, Q.; Ling, X. Camptothecin (CPT) and its derivatives are known to target topoisomerase I (Top1) as their mechanism of action: Did we miss something in CPT analogue molecular targets for treating human disease such as cancer? Am. J. Cancer Res. 2017, 7, 2350. [Google Scholar]
  35. Dini, I.; Soekamto, N.H.; Firdaus, F.; Supratman, U.; Latip, J. Alkaloid Caulerpin and Cytotoxic Activity against NCL-H460 Lung Cancer Cells Isolated along with β-sitosterol from the Halimeda cylindracea Decaisne. Sains Malays. 2021, 50, 2663–2674. [Google Scholar] [CrossRef]
  36. Mert-Ozupek, N.; Calibasi-Kocal, G.; Olgun, N.; Basbinar, Y.; Cavas, L.; Ellidokuz, H. An Efficient and Quick Analytical Method for the Quantification of an Algal Alkaloid Caulerpin Showed In-Vitro Anticancer Activity against Colorectal Cancer. Mar. Drugs 2022, 20, 757. [Google Scholar] [CrossRef]
  37. Hu, S.; Yin, J.; Yan, S.; Hu, P.; Huang, J.; Zhang, G.; Wang, F.; Tong, Q.; Zhang, Y. Chaetocochin J, an epipolythiodioxopiperazine alkaloid, induces apoptosis and autophagy in colorectal cancer via AMPK and PI3K/AKT/mTOR pathways. Bioorg. Chem. 2021, 109, 104693. [Google Scholar] [CrossRef] [PubMed]
  38. Xu, G.B.; He, G.; Bai, H.H.; Yang, T.; Zhang, G.L.; Wu, L.W.; Li, G.Y. Indole alkaloids from Chaetomium globosum. J. Nat. Prod. 2015, 78, 1479–1485. [Google Scholar] [CrossRef]
  39. Becer, E.; Hanoğlu, D.Y.; Kabadayı, H.; Hanoğlu, A.; Vatansever, S.; Yavuz, D.Ö.; Meriçli, F.; Meriçli, A.H. The effect of Colchicum pusillum in human colon cancer cells via Wnt/β-catenin pathway. Gene 2019, 686, 213–219. [Google Scholar] [CrossRef]
  40. Sun, G.C.; Chen, H.H.; Liang, W.Z.; Jan, C.R. Exploration of the effect of the alkaloid colchicine on Ca2+ handling and its related physiology in human oral cancer cells. Arch. Oral Biol. 2019, 102, 179–185. [Google Scholar] [CrossRef]
  41. Wang, Z.W.; Liu, H.; Ye, G.T.; Sheng, Z.Y.; Hu, Y.F.; Tan, Y.F.; Li, G.X. Crebanine N-oxide, a natural aporphine alkaloid isolated from Stephania hainanensis, induces apoptosis and autophagy in human gastric cancer SGC-7901 cells. Asian Pac. J. Trop. Biomed. 2020, 10, 224. [Google Scholar]
  42. Chai, F.; Zhou, J.; Chen, C.; Xie, S.; Chen, X.; Su, P.; Shi, J. The Hedgehog inhibitor cyclopamine antagonizes chemoresistance of breast cancer cells. Onco. Targets Ther. 2013, 6, 1643–1647. [Google Scholar]
  43. Lu, J.; Sun, D.; Gao, S.; Gao, Y.; Ye, J.; Liu, P. Cyclovirobuxine D induces autophagy-associated cell death via the Akt/mTOR pathway in MCF-7 human breast cancer cells. J. Pharmacol. Sci. 2014, 125, 74–82. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  44. Zulpa, A.K.; Muttiah, B.; Vellasamy, K.M.; Mariappan, V.; Vadivelu, J. Dentatin triggers ROS-mediated apoptosis, G0/G1 cell cycle arrest and release of Th1-related cytokines in colorectal carcinoma cells. J. Taibah Univ. Sci. 2023, 17, 2194231. [Google Scholar] [CrossRef]
  45. Andas, A.; Abdul, A.B.; Rahman, H.S.; Sukari, M.A.; Abdelwahab, S.I.; Samad, N.A.; Anasamy, T.; Arbab, I.A. Dentatin from clausena excavata induces apoptosis in HEPG2 cells via mitochondrial mediated signaling. Asian Pac. J. Cancer Prev. 2015, 16, 4311–4316. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  46. Yang, L.; Yu, X. Naturally occurring Girinimbine alkaloid inhibits the proliferation, migration, and invasion of human breast cancer cells via induction of apoptosis and inhibition of MEK/ERK and STAT3 signalling pathways. Acta Biochim Pol. 2021, 68, 647–652. [Google Scholar] [CrossRef]
  47. Satyavarapu, E.M.; Sinha, P.K.; Mandal, C. Influence of geographical and seasonal variations on carbazole alkaloids distribution in Murraya koenigii: Deciding factor of its in vitro and in vivo efficacies against cancer cells. Biomed Res Intl. 2020, 2020, 7821913. [Google Scholar] [CrossRef] [Green Version]
  48. Xie, H.; Zhang, T.; Yang, N.; Li, Z.; Liu, Y. Anticancer effects of Mahanimbine alkaloid on the human bladder cancer cells are due to the induction of G0/G1 cell cycle arrest, apoptosis and autophagy. J. BUON 2020, 25, 1166–1171. [Google Scholar]
  49. Still, P.C.; Yi, B.; González-Cestari, T.F.; Pan, L.; Pavlovicz, R.E.; Chai, H.-B.; Ninh, T.N.; Li, C.; Soejarto, D.D.; McKay, D.B. Alkaloids from Microcos paniculata with cytotoxic and nicotinic receptor antagonistic activities. J. Nat. Prod. 2013, 76, 243–249. [Google Scholar] [CrossRef] [Green Version]
  50. Dasari, S.; Bakthavachalam, V.; Chinnapaka, S.; Venkatesan, R.; Samy, A.L.; Munirathinam, G. Neferine, an alkaloid from lotus seed embryo targets HeLa and SiHa cervical cancer cells via pro-oxidant anticancer mechanism. Phytother. Res. 2020, 34, 2366–2384. [Google Scholar] [CrossRef]
  51. Tosun, F.; Mıhoğlugil, F.; Beutler, J.A.; Eroğlu Özkan, E.; Miski, M. Neopapillarine, an unusual coumarino-alkaloid from the root extract of neocryptodiscus papillaris with cytotoxic activity on renal cancer cells. Molecules 2020, 25, 3040. [Google Scholar] [CrossRef]
  52. Grabarska, A.; Wróblewska-Łuczka, P.; Kukula-Koch, W.; Łuszczki, J.J.; Kalpoutzakis, E.; Adamczuk, G.; Skaltsounis, A.L.; Stepulak, A. Palmatine, a bioactive protoberberine alkaloid isolated from berberis cretica, inhibits the growth of human estrogen receptor-positive breast cancer cells and acts synergistically and additively with doxorubicin. Molecules 2021, 26, 6253. [Google Scholar] [CrossRef]
  53. Awasthee, N.; Shekher, A.; Rai, V.; Verma, S.S.; Mishra, S.; Dhasmana, A.; Gupta, S.C. Piperlongumine, a piper alkaloid, enhances the efficacy of doxorubicin in breast cancer: Involvement of glucose import, ROS, NF-κB and lncRNAs. Apoptosis 2022, 27, 261–282. [Google Scholar] [CrossRef]
  54. Kumar, S.; Agnihotri, N. Piperlongumine, a piper alkaloid targets Ras/PI3K/Akt/mTOR signaling axis to inhibit tumor cell growth and proliferation in DMH/DSS induced experimental colon cancer. Biomed. Pharmacother. 2019, 109, 1462–1477. [Google Scholar] [CrossRef] [PubMed]
  55. Fadaeinasab, M.; Karimian, H.; Omar, H.; Taha, H.; Khorasani, A.; Banisalam, B.; Aziz Ketuly, K.; Abdullah, Z. Reflexin A, a new indole alkaloid from Rauvolfia reflexa induces apoptosis against colon cancer cells. J. Asian Nat. Prod. Res. 2020, 22, 474–488. [Google Scholar] [CrossRef] [PubMed]
  56. Burger, T.; Mokoka, T.; Fouché, G.; Steenkamp, P.; Steenkamp, V.; Cordier, W. Solamargine, a bioactive steroidal alkaloid isolated from Solanum aculeastrum induces non-selective cytotoxicity and P-glycoprotein inhibition. BMC Complement. Altern. Med. 2018, 18, 137. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  57. Wu, X.; Zheng, S.; Yan, Z.; Chen, S.; Zhang, W.; Miao, L.; Zhang, X. Inductive effect of solamargine on the apoptosis of human esophageal cancer KYSE150 cells and its action mechanism. J. Med. Postgrad. 2019, 12, 803–808. [Google Scholar]
  58. Qu, X.; Xie, J.; Zhang, Y.; Wang, Z. Solamargine Alleviates Proliferation and Metastasis of Cervical Cancer Cells by Blocking the CXCL3-Mediated Erk Signaling Pathway. Evid. Based Complement. Alternat. Med. 2022, 2022, 7634754. [Google Scholar] [CrossRef] [PubMed]
  59. Ge, J.; Wang, P.; Ma, H.; Zhang, J. Solamargine inhibits prostate cancer cell growth and enhances the therapeutic efficacy of docetaxel via Akt signaling. J. Oncol. 2022, 2022, 1–11. [Google Scholar] [CrossRef]
  60. Fu, R.; Wang, X.; Hu, Y.; Du, H.; Dong, B.; Ao, S.; Zhang, L.; Sun, Z.; Zhang, L.; Lv, G. Solamargine inhibits gastric cancer progression by regulating the expression of lncNEAT1_2 via the MAPK signaling pathway. Int. J. Oncol. 2019, 54, 1545–1554. [Google Scholar] [CrossRef] [Green Version]
  61. Noulala, C.G.T.; Ouete, J.L.N.; Atangana, A.F.; Mbahbou, G.T.B.; Fotso, G.W.; Stammler, H.-G.; Lenta, B.N.; Happi, E.N.; Sewald, N.; Ngadjui, B.T. Soyauxinine, a New Indolopyridoquinazoline Alkaloid from the Stem Bark of Araliopsis soyauxii Engl. (Rutaceae). Molecules 2022, 27, 1104. [Google Scholar] [CrossRef]
  62. Noulala, C.G.T.; Fotso, G.W.; Rennert, R.; Lenta, B.N.; Sewald, N.; Arnold, N.; Happi, E.N.; Ngadjui, B.T. Mesomeric form of quaternary indoloquinazoline alkaloid and other constituents from the Cameroonian Rutaceae Araliopsis soyauxii Engl. Biochem. Syst. Ecol. 2020, 91, 104050. [Google Scholar] [CrossRef]
  63. Mbaveng, A.T.; Noulala, C.G.; Samba, A.R.; Tankeo, S.B.; Abdelfatah, S.; Fotso, G.W.; Happi, E.N.; Ngadjui, B.T.; Beng, V.P.; Kuete, V. The alkaloid, soyauxinium chloride, displays remarkable cytotoxic effects towards a panel of cancer cells, inducing apoptosis, ferroptosis and necroptosis. Chem. Biol. Interact. 2021, 333, 109334. [Google Scholar] [CrossRef]
  64. Hamid, H.A.; Ramli, A.N.; Yusoff, M.M. Indole alkaloids from plants as potential leads for antidepressant drugs: A mini review. Front. Pharmacol. 2017, 8, 96. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  65. Matada, B.S.; Pattanashettar, R.; Yernale, N.G. A comprehensive review on the biological interest of quinoline and its derivatives. Bioorg. Med. Chem. 2021, 32, 115973. [Google Scholar] [CrossRef] [PubMed]
  66. Mathada, B.S. The Versatile Quinoline and Its Derivatives as anti-Cancer Agents: An Overview. Polycycl. Aromat. Compd. 2022, 43, 4333–4345. [Google Scholar] [CrossRef]
  67. Ilakiyalakshmi, M.; Napoleon, A.A. Review on recent development of quinoline for anticancer activities. Arab. J. Chem. 2022, 15, 104168. [Google Scholar] [CrossRef]
  68. Liu, K.; Ding, X.; Deng, B.; Chen, W. 10-Hydroxycamptothecin produced by a new endophytic Xylaria sp., M20, from Camptotheca acuminata. Biotechnol. Lett. 2010, 32, 689–693. [Google Scholar] [CrossRef]
  69. Georgiades, S.N.; Nicolaou, P.G. Recent advances in carbazole syntheses. Adv. Heterocycl. Chem. 2019, 129, 1–88. [Google Scholar]
  70. Khandokar, L.; Bari, M.S.; Seidel, V.; Haque, M.A. Ethnomedicinal uses, phytochemistry, pharmacological activities and toxicological profile of Glycosmis pentaphylla (Retz.) DC.: A review. J. Ethnopharmacol. 2021, 278, 114313. [Google Scholar] [CrossRef]
  71. Chen, Y.; Tang, C.; Wu, Y.; Mo, S.; Wang, S.; Yang, G.; Mei, Z. Glycosmisines A and B: Isolation of two new carbazole–indole-type dimeric alkaloids from Glycosmis pentaphylla and an evaluation of their antiproliferative activities. Org. Biomol. Chem. 2015, 13, 6773–6781. [Google Scholar] [CrossRef]
  72. Huang, L.; Zhe-Ling, F.; Yi-Tao, W.; Li-Gen, L. Anticancer carbazole alkaloids and coumarins from Clausena plants: A review. Chin. J. Nat. Med. 2017, 15, 881–888. [Google Scholar] [CrossRef]
  73. Xia, H.M.; Yang, G.Q.O.; Li, C.J.; Yang, J.Z.; Ma, J.; Zhang, D.; Li, Y.; Li, L.; Zhang, D.M. Clauemarazoles A–G, seven carbazole alkaloids from the stems of Clausena emarginata. Fitoterapia 2015, 103, 83–89. [Google Scholar] [CrossRef]
  74. Sun, X.Y.; Ma, J.; Li, C.J.; Zang, Y.D.; Huang, J.W.; Wang, X.Y.; Chen, N.H.; Chen, X.G.; Zhang, D.M. Carbazole alkaloids with bioactivities from the stems of Clausena lansium. Phytochem. Lett. 2020, 38, 28–32. [Google Scholar] [CrossRef]
  75. Maneerat, W.; Phakhodee, W.; Cheenpracha, S.; Ritthiwigrom, T.; Deachathai, S.; Laphookhieo, S. Clausenawallines G–K, carbazole alkaloids from Clausena wallichii twigs. Phytochemistry 2013, 88, 74–78. [Google Scholar] [CrossRef]
  76. Huang, Y.; Li, G.; Hong, C.; Zheng, X.; Yu, H.; Zhang, Y. Potential of Steroidal Alkaloids in Cancer: Perspective Insight into Structure–Activity Relationships. Front. Oncol. 2021, 11, 733369. [Google Scholar] [CrossRef]
  77. Abd Karim, H.A.; Ismail, N.H.; Osman, C.P. Steroidal Alkaloids from the Apocynaceae Family: Their Isolation and Biological Activity. Nat. Prod. Commun. 2022, 17, 1934578X221141265. [Google Scholar] [CrossRef]
  78. Eshonov, M.; Turgunov, K.; Tashkhodzhaev, B.; Shakirov, R. Alkaloids of Buxus sempervirens, crystal and molecular structure of Cyclobuxine-D and Imperialine. Chem. Nat. Compd. 2014, 49, 1179–1182. [Google Scholar] [CrossRef]
  79. Phi, T.D.; Pham, V.C.; Thi Mai, H.D.; Litaudon, M.; Guéritte, F.O.; Nguyen, V.H.; Chau, V.M. Cytotoxic steroidal alkaloids from Kibatalia laurifolia. J. Nat. Prod. 2011, 74, 1236–1240. [Google Scholar] [CrossRef] [PubMed]
  80. Turner, M.W.; Cruz, R.; Mattos, J.; Baughman, N.; Elwell, J.; Fothergill, J.; Nielsen, A.; Brookhouse, J.; Bartlett, A.; Malek, P. Cyclopamine bioactivity by extraction method from Veratrum californicum. Bioorg. Med. Chem. 2016, 24, 3752–3757. [Google Scholar] [CrossRef] [PubMed]
  81. Singh, L.; Upadhyay, A.K.; Dixit, P.; Singh, A.; Yadav, D.; Chhavi, A.; Konar, S.; Srivastava, R.P.; Pandey, S.; Devkota, H.P. A review of chemistry and pharmacology of Piperidine alkaloids of Pinus and related genera. Curr. Pharm. Biotechnol. 2022, 23, 1132–1141. [Google Scholar] [PubMed]
  82. Mitra, S.; Anand, U.; Jha, N.K.; Shekhawat, M.S.; Saha, S.C.; Nongdam, P.; Rengasamy, K.R.; Proćków, J.; Dey, A. Anticancer applications and pharmacological properties of piperidine and piperine: A comprehensive review on molecular mechanisms and therapeutic perspectives. Front. Pharmacol. 2022, 12, 772418. [Google Scholar] [CrossRef]
  83. Song, L.; Wang, Y.; Zhen, Y.; Li, D.; He, X.; Yang, H.; Zhang, H.; Liu, Q. Piperine inhibits colorectal cancer migration and invasion by regulating STAT3/Snail-mediated epithelial–mesenchymal transition. Biotechnol. Lett. 2020, 42, 2049–2058. [Google Scholar] [CrossRef] [PubMed]
  84. Arun, A.; Ansari, M.; Popli, P.; Jaiswal, S.; Mishra, A.; Dwivedi, A.; Hajela, K.; Konwar, R. New piperidine derivative DTPEP acts as dual-acting anti-breast cancer agent by targeting ER α and downregulating PI 3K/Akt-PKC α leading to caspase-dependent apoptosis. Cell Prolif. 2018, 51, e12501. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  85. Dragull, K.; Yoshida, W.Y.; Tang, C.S. Piperidine alkaloids from Piper methysticum. Phytochemistry 2003, 63, 193–198. [Google Scholar] [CrossRef] [PubMed]
  86. Viegas, C.; Bolzani, V.D.S.; Furlan, M.; Barreiro, E.J.; Young, M.C.M.; Tomazela, D.; Eberlin, M.N. Further Bioactive Piperidine Alkaloids from the Flowers and Green Fruits of Cassia s pectabilis. J. Nat. Prod. 2004, 67, 908–910. [Google Scholar] [CrossRef] [PubMed]
  87. Zhang, G.; Zhang, N.; Xu, L.; Wu, H.T.; Chen, D.; Lin, Q.H.; Luo, L.Z. A new piperidine alkaloid from the leaves of Microcos paniculata L. Nat. Prod. Res. 2017, 31, 169–174. [Google Scholar] [CrossRef]
  88. Sears, J.E.; Boger, D.L. Total synthesis of vinblastine, related natural products, and key analogues and development of inspired methodology suitable for the systematic study of their structure–function properties. Acc. Chem. Res. 2015, 48, 653–662. [Google Scholar] [CrossRef] [Green Version]
  89. Tilaoui, M.; Ait Mouse, H.; Zyad, A. Update and new insights on future cancer drug candidates from plant-based alkaloids. Front. Pharmacol. 2021, 12, 3621. [Google Scholar] [CrossRef]
  90. O’Brien, S.; Kantarjian, H.; Keating, M.; Beran, M.; Koller, C.; Robertson, L.; Hester, J.; Rios, M.; Andreeff, M.; Talpaz, M. Homoharringtonine therapy induces responses in patients with chronic myelogenous leukemia in late chronic phase. Blood 1995, 86, 3322–3326. [Google Scholar] [CrossRef]
  91. Wang, Q.; Ding, W.; Ding, Y.; Ma, J.; Qian, Z.; Shao, J.; Li, Y. Homoharringtonine suppresses imatinib resistance via the Bcl-6/p53 pathway in chronic myeloid leukemia cell lines. Oncotarget 2017, 8, 37594. [Google Scholar] [CrossRef]
  92. Chen, X.; Tang, Y.; Chen, J.; Chen, R.; Gu, L.; Xue, H.; Pan, C.; Tang, J.; Shen, S. Homoharringtonine is a safe and effective substitute for anthracyclines in children younger than 2 years old with acute myeloid leukemia. Front. Med. 2019, 13, 378–387. [Google Scholar] [CrossRef]
  93. Ahmadi, S.E.; Rahimi, S.; Zarandi, B.; Chegeni, R.; Safa, M. MYC: A multipurpose oncogene with prognostic and therapeutic implications in blood malignancies. J. Hematol. Oncol. 2021, 14, 121. [Google Scholar] [CrossRef]
  94. Chen, X.J.; Zhang, W.N.; Chen, B.; Xi, W.D.; Lu, Y.; Huang, J.Y.; Wang, Y.Y.; Long, J.; Wu, S.F.; Zhang, Y.X.; et al. Homoharringtonine deregulates MYC transcriptional expression by directly binding NF-κB repressing factor. Proc. Natl. Acad. Sci. USA 2019, 116, 2220–2225. [Google Scholar] [CrossRef] [Green Version]
  95. Ávila-Gálvez, M.Á.; García-Villalba, R.; Martínez-Díaz, F.; Ocaña-Castillo, B.; Monedero-Saiz, T.; Torrecillas-Sánchez, A.; Abellán, B.; González-Sarrías, A.; Espín, J.C. Metabolic profiling of dietary polyphenols and methylxanthines in normal and malignant mammary tissues from breast cancer patients. Mol. Nutr. Food Res. 2019, 63, 1801239. [Google Scholar] [CrossRef] [PubMed]
  96. Chen, Y.X.; Gao, Q.Y.; Zou, T.H.; Wang, B.M.; Liu, S.D.; Sheng, J.Q.; Ren, J.L.; Zou, X.P.; Liu, Z.J.; Song, Y.Y. Berberine versus placebo for the prevention of recurrence of colorectal adenoma: A multicentre, double-blinded, randomised controlled study. Lancet Gastroenterol. Hepatol. 2020, 5, 267–275. [Google Scholar] [CrossRef] [PubMed]
  97. Lu, J.J.; Bao, J.L.; Chen, X.P.; Huang, M.; Wang, Y.T. Alkaloids isolated from natural herbs as the anticancer agents. Evid. Based Complement. Alternat. Med. 2012, 2012, 485042. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  98. Sindhoor, S.; Naveen, N.R.; Rao, G.K.; Gopan, G.; Chopra, H.; Park, M.N.; Alshahrani, M.M.; Jose, J.; Emran, T.B.; Kim, B. A spotlight on alkaloid nanoformulations for the treatment of lung cancer. Front. Oncol. 2022, 12, 994155. [Google Scholar]
  99. Lee, R.J.; Low, P.S. Folate-mediated tumor cell targeting of liposome-entrapped doxorubicin in vitro. Biochim. Biophys. Acta Biomembr. 1995, 1233, 134–144. [Google Scholar] [CrossRef] [Green Version]
  100. Makwana, V.; Karanjia, J.; Haselhorst, T.; Anoopkumar-Dukie, S.; Rudrawar, S. Liposomal doxorubicin as targeted delivery platform: Current trends in surface functionalization. Int. J. Pharm. 2021, 593, 120117. [Google Scholar] [CrossRef]
  101. Berger, W.; Setinek, U.; Hollaus, P.; Zidek, T.; Steiner, E.; Elbling, L.; Cantonati, H.; Attems, J.; Gsur, A.; Micksche, M. Multidrug resistance markers P-glycoprotein, multidrug resistance protein 1, and lung resistance protein in non-small cell lung cancer: Prognostic implications. J. Cancer Res. Clin. Oncol. 2005, 131, 355–363. [Google Scholar] [CrossRef]
  102. Etievant, C.; Barret, J.M.; Kruczynski, A.; Perrin, D.; Hill, B.T. Vinflunine (20′,20′-difluoro-3′,4′-dihydrovinorelbine), a novel Vinca alkaloid, which participates in P-glycoprotein (Pgp)-mediated multidrug resistance in vivo and in vitro. Invest. New Drugs. 1998, 16, 3–17. [Google Scholar] [CrossRef]
  103. Schramm, S.; Köhler, N.; Rozhon, W. Pyrrolizidine alkaloids: Biosynthesis, biological activities and occurrence in crop plants. Molecules 2019, 24, 498. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  104. Zhao, Y.; Wang, S.; Xia, Q.; da Costa, G.C.A.; Doerge, D.R.; Cai, L.; Fu, P.P. Reaction of dehydropyrrolizidine alkaloids with valine and hemoglobin. Chem. Res. Toxicol. 2014, 27, 1720–1731. [Google Scholar] [CrossRef] [PubMed]
  105. Kurimoto, M.; Chang, T.C.; Nishiyama, Y.; Suzuki, T.; Dohmae, N.; Tanaka, K.; Yokoshima, S. Anticancer Approach Inspired by the Hepatotoxic Mechanism of Pyrrolizidine Alkaloids with Glycosylated Artificial Metalloenzymes. Angew. Chem. 2022, 134, e202205541. [Google Scholar] [CrossRef]
Molecules 28 05578 g001 550
Figure 1. Alkaloids and their general pharmacological significance.
Figure 1. Alkaloids and their general pharmacological significance.
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Molecules 28 05578 g002 550
Figure 2. Structural diversity of alkaloids characterized from various plants.
Figure 2. Structural diversity of alkaloids characterized from various plants.
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Molecules 28 05578 g003 550
Figure 3. Cancer tissue targets of plant-derived alkaloids (images adapted from https://app.biorender.com/ (accessed on 14 June 2023)).
Figure 3. Cancer tissue targets of plant-derived alkaloids (images adapted from https://app.biorender.com/ (accessed on 14 June 2023)).
Molecules 28 05578 g003
Table
Table 1. Anticancer alkaloids identified form different plant species.
Table 1. Anticancer alkaloids identified form different plant species.
CompoundStructural
Classification		Plant SourcePlant FamilyMode of Action References
3-Methoxy carbazoleCarbazole
alkaloid		Glycosmis arboreaRutaceae
  • Increased reactive oxygen species production and caspase 3 protein expression in MCF-7 cells
[23,24]
3,10-DibromofascaplysinIndole
alkaloid		Fascaplysinopsis reticulataThorectidae
  • Inhibition of androgen receptor signaling
  • Activation of C-jun N-terminal kinase (JNK) in prostate cancer cells
[25,26]
6-MethoxydihydroavicineIsoquinoline alkaloidsMacleaya cordataPapaveraceae
  • Activation of receptor-interacting serine/threonine protein kinase 1 and alteration of oxaloacetic acid metabolism and pancreatic cancer cells
  • Stimulation of reactive oxygen species activation of mitogen-activated protein kinase pathway in ovarian cancer cells
[27,28]
6, 7-Dimethoxy-1-(α-hydroxy-4-methoxybenzyl)-2-methyl-1, 2, 3, 4-tetrahydroisoquinolineBenzylisoquinoline alkaloidAnnona squamosaAnnonaceaeNA[29]
AcetoxytabernosineIndole
alkaloid		Alstonia
yunnanensis		Apocynaceae
  • Promotion of caspase 3- and caspase 9-mediated apoptosis in hepatocellular carcinoma cells
[30]
CamptothecinPyrroloquinoline alakloidCamptotheca
acuminata		Nyssaceae
  • Inhibition of topoisomerase 1 and BRD4 in MDA-MB-231 breast cancer cells
[31,32]
CaulerpinIndole
alkaloid		Halimeda
cylindracea,
Halimeda
lentillifera		Halimedaceae
  • Enhancement of cell migration and induction of apoptosis in colorectal cancer cells
[33,34]
Chaetocochin JIndole
alkaloid		Chaetomium
globosum		Chaetomiaceae
  • Induction of autophagy via activation of PI3K/AKT/mTOR pathway in colorectal cancer cells
[35,36]
CoclaurineBenzylisoquinoline alkaloidAnnona squamosaAnnonaceaeNA[29]
ColchicineProto-alkaloidColchicum
pusillum
Colchicum
autumnale		Colchicaceae
Liliaceae
  • Induction of apoptosis by increasing P53, BAX and caspase 3 and 9 protein expression in breast cancer cells
  • Significant increase in cytosolic Ca2+ concentration by activation of phospholipase C in oral cancer cells
[37,38,39]
Crebanine N-oxideAporphine alkaloidStephania
hainanensis		Menispermaceae
  • G2 phase cell cycle arrest
  • Increase in the expression of cytochrome c and caspase 3 in gastric cancer cells
[40]
Cyclopamine Steroidal
alkaloid		Veratrum
californicum		Liliaceae
  • Inhibition of hedgehog signaling cascade by altering Smo protein function
[41]
Cyclovirobuxine DSteroidal
alkaloid 		Buxus
sempervirens		Buxaceae
  • Increase in ATG5 protein expression and suppression of Akt/mTOR signaling pathway in breast cancer cells
[42]
DentatinCarbazole
alkaloid		Clausena excavateRutaceae
  • Elevation of Th1 cytokine protein expression
  • Suppression of NF-κB and activation of caspase 3 and 9 in HepG2 cells
[43,44]
GirinimbineCarbazole
alkaloid		Murraya koenigiiRutaceae
  • Inhibition of MEK/ERK pathway
  • Downregulation of Bcl-2 in breast cancer cells
[45]
KoenimbineCarbazole
alkaloid		Murraya koenigiiRutaceae
  • Disruption of energy metabolism in prostate cancer cells
[46]
MahanimbineCarbazole
alkaloid		Murraya koenigiiRutaceae
  • Arrest of G0/G1 phase cell cycle through reduction in cyclin E and cyclin D1-D3 expression in bladder cancer cells
[46,47]
MahanineCarbazole
alkaloid		Murraya koenigiiRutaceae
  • Oxidative stress-mediated activation of LC3 proteins
  • Reduction in p62 expression in ovarian cancer cells
[46]
Microcosamine A Piperidine
alkaloids		Microcos
paniculate		Malvaceae
  • Inhibition of nicotinic acetylcholine receptors in colon cancer cells
[48]
NeferineBenzylisoquinoline alkaloidNelumbo nuciferaNelumbonaceae
  • Increase in cellular generation of ROS and elevated expression of cytochrome c in cervical cancer cells
[49]
NeopapillarineCumarino alkaloidNeocryptodiscus papillarisApiaceaeNA[50]
PalmatineIsoquinoline alkaloidsBerberis creticaBerberidaceae
  • Suppression of estrogen receptor signaling in breast cancer cells
[51]
PiperlonguminePiperidine
alkaloid		Piper longumPiperaceae
  • Inhibition of glucose transport and TNF-α-induced NF-κB activation in breast cancer cells
  • Reduction in Bcl-2 expression in colonocytes of rats with colon cancer
[52,53]
Reflexin AIndole
alkaloid		Rauvolfia reflexaApocynaceae
  • Induction of G1 cell cycle arrest
  • Activation of apoptotic caspases in colon cancer cells
[54]
SolamargineSteroidal
alkaloid		Solanum
aculeastrum
Solanum nigrum		Solanaceae
  • Interference with PI3K/Akt signaling in prostate carcinoma
  • Reduction in NEAT1 protein levels in gastric cancer cells
  • Inhibition of P-glycoprotein in neuroblastoma cells
[55,56,57,58,59]
SoyauxinineIndoloquinazoline alkaloidAraliopsis
soyauxii		Rutaceae
  • Alteration of mitochondria membrane polarization and increased ROS production in leukemia cells
[60,61,62]
NA = Not available in the cited article.
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Olofinsan, K.; Abrahamse, H.; George, B.P. Therapeutic Role of Alkaloids and Alkaloid Derivatives in Cancer Management. Molecules 2023, 28, 5578. https://doi.org/10.3390/molecules28145578

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Olofinsan K, Abrahamse H, George BP. Therapeutic Role of Alkaloids and Alkaloid Derivatives in Cancer Management. Molecules. 2023; 28(14):5578. https://doi.org/10.3390/molecules28145578

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Olofinsan, Kolawole, Heidi Abrahamse, and Blassan P. George. 2023. "Therapeutic Role of Alkaloids and Alkaloid Derivatives in Cancer Management" Molecules 28, no. 14: 5578. https://doi.org/10.3390/molecules28145578

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