Home A review of the mechanisms of anti-cancer activities of some medicinal plants–biochemical perspectives
Article
Licensed
Unlicensed Requires Authentication

A review of the mechanisms of anti-cancer activities of some medicinal plants–biochemical perspectives

  • Patrick E. Aba EMAIL logo , John I. Ihedioha and Isaac U. Asuzu
Published/Copyright: December 16, 2021

Abstract

Cancer is a disease resulting in unbridled growth of cells due to dysregulation in the balance of cell populations. Various management procedures in handling cases of cancer are not without their adverse side effects on the normal cells. Medicinal plants/herbs have been in use in the management of various ailments, including cancer, for a long time. Medicinal plants have been credited with wide safety margins, cost effectiveness, availability and diverse activities. This study reviewed various mechanisms of anti-cancer activities of some medicinal plants from a biochemical perspective. The mechanisms of anti-cancer activities of plant compounds addressed in this article include induction of apoptosis, anti-angiogenic effects, anti-metastasis, inhibition of cell cycle, inhibition of DNA destruction and effects on key enzymes, cytotoxic and anti-oxidant effects. The anti-cancer activities of some of the plants involve more than one mechanism.


Corresponding author: Patrick E. Aba, Department of Veterinary Physiology and Pharmacology, University of Nigeria, Nsukka, Enugu State, Nigeria, Phone:+2348062730072, E-mail:

  1. Research funding: None declared.

  2. Competing interest: Authors declare no competing interest. Funding organization did not play any role in the literature search or report writing or in the decision to submit the report for publication.

  3. Employment/leadership: None declared.

  4. Honorarium: None declared.

  5. Author contributions: All authors contributed to writing and revising the manuscript and have accepted responsibility for the entire content of the submitted manuscript. They approved submission.

References

1. Smeltzer, SC, Bare, BG, Hinkle, JL, Cheever, KH. Brunner and Suddarth’s textbook of medical surgical nursing, 12th ed.London, England: Wolters Kluwer; 2010:205–31pp.Search in Google Scholar

2. Kumar, V, Abbas, A, Aster, J. Robbins pathologic basis of disease, 9th ed.Tehran, Iran: Arjomand; 2014.Search in Google Scholar

3. Lachenmayer, A, Alsinet, C, Chang, CY, Liovit, JM. Molecular approaches to treatment of hepatocellular carcinoma. Dig Liver Dis2010;42:264–72. https://doi.org/10.1016/S1590-8658(10)60515-4.Search in Google Scholar PubMed PubMed Central

4. Kooti, W, Hasanzadeh-Noohi, Z, Sharafi-Ahvazi, N, Asadi-Samani, M, Ashtary-Larky, D. Phytochemistry, pharmacology, and therapeutic uses of black seed (Nigella sativa). Chin J Nat Med2016;14:732–45. https://doi.org/10.1016/s1875-5364(16)30088-7.Search in Google Scholar

5. Jedy-Agba, E, Curado, MP, Ogunbiyi, O, Oga, E, Fabowale, T, Igbinoba, F, et al.. Cancer incidence in Nigeria: a report from population-based cancer registries. Cancer Epidemiol2012;36:271–8. https://doi.org/10.1016/j.canep.2012.04.007.Search in Google Scholar PubMed PubMed Central

6. Vasudevan, D, Valdyanathan, K. Biochemistry of cancer. In: Textbook of biochemistry. New Delhi: Indian Council of Medical Research; 2017:603–13 pp.Search in Google Scholar

7. Merlo, LM, Pepper, JW, Reid, BJ, Maley, CC. Cancer as an evolutionary and ecological process. NatRev Cancer2006;6:924–35. https://doi.org/10.1038/nrc2013.Search in Google Scholar PubMed

8. Baylin, SB, Ohm, JE. Epigenetic gene silencing in cancer – a mechanism for early oncogenic pathway addiction?Nat Rev Cancer2006;6:107–16. https://doi.org/10.1038/nrc1799.Search in Google Scholar PubMed

9. Lemoine, NK, Nicholas, R. Progress in pathology. London: Greenwich Medical Media; 2001.Search in Google Scholar

10. Sondak, VK, Chang, AE. Clinical evaluation and treatment of soft tissue tumors. In: Weiss, SW, Goldblum, JR, editors. Enzinger and Weiss’s soft tissue tumors, 4th ed.Philadelphia, PA: Mosby; 2001.10.1097/00125480-200209000-00010Search in Google Scholar

11. Mankin, HJ, Hornicek, FJ. Diagnosis, classification, and management of soft tissue sarcomas.Can Contract2005;12:5–21. https://doi.org/10.1177/107327480501200102.Search in Google Scholar PubMed

12. Freedman, A. Follicular lymphoma: 2012 update on diagnosis and management. Am J Hematol2012;87:988–95. https://doi.org/10.1002/ajh.23313.Search in Google Scholar PubMed

13. Nastoupil, LJ, Rose, AC, Flowers, CR. Diffuse large B-cell lymphoma: current treatment approaches. Oncology2012;26:488–95.Search in Google Scholar

14. Kooti, W, Servatyari, K, Behzadifar, M, Asadi-Samani, M, Sadeghi, F, Nouri, B, et al.. Effective medicinal plant in cancer treatment part 2: review study. J Evidbase Compl Alter Med 2017;22:982–95. https://doi.org/10.1177/2156587217696927.Search in Google Scholar PubMed PubMed Central

15. Levy, MH, Back, A, Bazargan, S, Benedetti, C, Billings, JA, Block, S, et al.. Palliative care. Clinical practice guidelines in oncology.J Natl Compr Cancer Netw2006;4:776–818. https://doi.org/10.6004/jnccn.2006.0068.Search in Google Scholar PubMed

16. Montazeri, A. Quality of life data as prognostic indicators of survival in cancer patients: an overview of the literature from 1982 to 2008. Health Qual Life Outcome2009;7:102. https://doi.org/10.1186/1477-7525-7-102.Search in Google Scholar PubMed PubMed Central

17. Amin, AR, Kucuk, O, Khuri, FR, Shin, DM. Perspectives for cancer prevention with natural compounds. J ClinOncol2009;27:2712–25. https://doi.org/10.1200/jco.2008.20.6235.Search in Google Scholar PubMed PubMed Central

18. BaiShen, WE, Hu, B. The induction of the apoptosis of cancer cell by sonodynamic therapy: a review. Chin J Cancer Res2012;24:368–73. https://doi.org/10.1007/s11670-012-0277-6.Search in Google Scholar

19. Bauer, JH, Hefand, SL. New tricks of an old molecule.Life span regulation by p53. Aging Cell 2006;5:437–40. https://doi.org/10.1111/j.1474-9726.2006.00228.x.Search in Google Scholar PubMed PubMed Central

20. Gasco, M, Shami, S, Cook, T. The p53 pathway in breast cancer. Breast Cancer Res 2002;4:70–6. https://doi.org/10.1186/bcr426.Search in Google Scholar PubMed PubMed Central

21. Li, J, Lee, B, Lee, AS. Endoplasmic reticulum stress-induced apoptosis: multiple pathways and activation of p53-up-regulated modulator of apoptosis (PUMA) and NOXA by p53. J BiolChem2006;281:7260–70. https://doi.org/10.1074/jbc.m509868200.Search in Google Scholar PubMed

22. Broeker, LE, Kruyt, FAE, Giaccone, G. Cell death independent of caspases: a review. ClinCancer Res Off J Am Assoc Cancer Res2005;11:3155–62.10.1158/1078-0432.CCR-04-2223Search in Google Scholar PubMed

23. Kumar, V, Abbas, AK, Fausto, N. Robbins and Cotran pathologic basis of disease, 8th ed.Philadelphia: SaundersElsevier Inc.; 2010:25–32pp.Search in Google Scholar

24. Hengartner, MO. Apoptosis: corralling the corpses. Cell2000;104:325–8.10.1016/S0092-8674(01)00219-7Search in Google Scholar PubMed

25. Lavrik, IN, Golks, A, Krammer, PH. Caspases; pharmacological manipulations of cell death modalities. J Clin Invest2005;115:2665–72. https://doi.org/10.1172/jci26252.Search in Google Scholar

26. Thomson, M, Ali, M. Garlic (Allium sativum): a review of its potential use as an anti-cancer agent. Curr Cancer Drug Targets2003;3:67–81. https://doi.org/10.2174/1568009033333736.Search in Google Scholar PubMed

27. Bianchini, F, Vainio, H. Allium vegetables and organosulfur compounds: do they help prevent cancer?Environ Health Perspect2001;109:893–902. https://doi.org/10.1289/ehp.01109893.Search in Google Scholar PubMed PubMed Central

28. DalaliIsfahani, L, Monajemi, R, Amjad, L. Cytotoxic effects of extract and essential oil leaves of Achilleawilhelmsii C. Koch on colon cancers cells. ExpAnimBiol2013;1:1–6.Search in Google Scholar

29. Harwansh, RK, Patra, KC, Pareta, SK, Singh, J. Pharmacological studies on Glycyrrhizaglabra. PharmacolOnline2011;2:1032–8.Search in Google Scholar

30. Torres, RG, Casanova, LM, Carvalho, J, Zancan, P. Ocimumbasilicum but not Ocimumgratissimum present cytotoxic effects on human breast cancer cell linMCF-7, inducing apoptosis and triggering mTOR/Akt/p7056K pathway. J BioenergBiomembr2018;50:1–13. https://doi.org/10.1007/s10863-018-9750-3.Search in Google Scholar PubMed

31. Kumar, V, Abbas, AK, Fausto, N. Robbins and Cotran pathologic basis of disease, 7th ed.Philadelphia: SaundersElsevier Inc.; 2004.Search in Google Scholar

32. Folkman, J. Tumor angiogenesis therapeutic implications. N Engl J Med1971;285:1182–6. https://doi.org/10.1056/NEJM197111182852108.Search in Google Scholar PubMed

33. Nishida, N, Yano, H, Nishida, T, Kamura, T, Kojiro, M. Angiogenesis in cancer. Vasc Health Risk Manag2006;2:213–9. https://doi.org/10.2147/vhrm.2006.2.3.213.Search in Google Scholar PubMed PubMed Central

34. Ahn, JB, Rha, SY, Shin, SJ, Jeung, HC, Kim, TS, Zhang, X, et al.. Circulating endothelial progenitor cells (EPC) for tumorvasculogenesis in gastric cancer patients. Cancer Lett2010;288:124–32. https://doi.org/10.1016/j.canlet.2009.06.031.Search in Google Scholar PubMed

35. Moccia, F, Zuccolo, E, Poletto, V, Cinelli, M, Bonetti, E, Guerra, G, et al.. Endothelial progenitor cells support tumour growth and metastatisation: implications for the resistance to anti-angiogenic therapy. Tumour Biol2015;36:6603–14. https://doi.org/10.1007/s13277-015-3823-2.Search in Google Scholar PubMed

36. Ono, M, Kosaka, N, Tominaga, N, Yoshioka, Y, Takeshita, F, Takahashi, RU, et al.. Exosomes from bone marrow mesenchymal stem cells contain a microRNA that promotes dormancy in metastatic breast cancer cells. Sci Signal2014;7:63. https://doi.org/10.1126/scisignal.2005231.Search in Google Scholar PubMed

37. Kim, KJ, Li, B, Winer, J, Armanini, M, Gillett, N, Phillips, HS, et al.. Inhibition of vascular endothelia growth factor-induced angiogenesis suppresses tumour growth in vivo. Nature1993;362:841–4. https://doi.org/10.1038/362841a0.Search in Google Scholar PubMed

38. Lippert, JW. Vascular disrupting agents.Bioorg Med Chem2007;15:605–15. https://doi.org/10.1016/j.bmc.2006.10.020.Search in Google Scholar PubMed

39. Stack, MS, Gately, S, Bafetti, LM, Enghild, JJ, Soff, GA. Angiostatin inhibits endothelial and melanoma cellular invasion by blocking matrix-enhanced plasminogen activation. Biochem J1999;340:77–84. https://doi.org/10.1042/bj3400077.Search in Google Scholar

40. Gordanian, B, Behbahani, M, Carapetian, J, Fazilati, M. Cytotoxic effect of Artemisia absinthium L. grown at two different altitudes on human breast cancer cell line MCF7. Pajouhesh Dar Pezeshki2012;36:124–31.Search in Google Scholar

41. Srivastava, R, Ahmed, H, Dixit, RK, Saraf, SA. Crocus sativus L. a comprehensive review. Pharmacogn Rev2010;4:200–8. https://doi.org/10.4103/0973-7847.70919.Search in Google Scholar PubMed PubMed Central

42. Halliwell, B, Gutteridge, JMC, Cross, CE. Free radicals, antioxidant and human disease, where are we now?J Lab Clin Med1992;119:598–620.Search in Google Scholar

43. Halliwell, B, Gutteridge, JMC. The antioxidant of human extracellular fluids.Arch BiochemBiophys1990;280:1–8. https://doi.org/10.1016/0003-9861(90)90510-6.Search in Google Scholar PubMed

44. Sindhi, V, Gupta, V, Sharma, K, Bhatnaja, S, Kumari, R, Dhaka, N. Potential applications of antioxidants-a review. J Pharm Res2013;7:828–35. https://doi.org/10.1016/j.jopr.2013.10.001.Search in Google Scholar

45. Marinescu, S, Anghel, R, Gruia, MI, Beuran, M. Involvement of reactive oxygen species in the mechanisms associated with cervical cancer specific treatment. Chirurgia (Bucur)2014;109:806–11.Search in Google Scholar

46. Sreevalsan, S, Safe, S. Reactive oxygen species and colorectal cancer. Curr Colorectal Cancer Rep2013;9:350–7. https://doi.org/10.1007/s11888-013-0190-5.Search in Google Scholar PubMed PubMed Central

47. Sena, LA, Chandel, NS. Physiological roles of mitochondrial reactive oxygen species.Mol Cell2012;48:158–67. https://doi.org/10.1016/j.molcel.2012.09.025.Search in Google Scholar PubMed PubMed Central

48. Raninga, PV, Trapani, GD, Tonissen, KF. Cross talk between two antioxidant systems, thioredoxin and DJ-1: consequences for cancer. Oncoscience2014;1:95–110. https://doi.org/10.18632/oncoscience.12.Search in Google Scholar PubMed PubMed Central

49. Simone, NL, Simone, V, Simone, CB. Antioxidants and other nutrients do not interfere with chemotherapy or radiation therapy and can increase kill and increase survival part II. Alternative Ther Health Med2007;13:22–8.Search in Google Scholar

50. Uttara, B, Singh, AV, Zamboni, P, Mahajan, RT. Oxidative stress and neurodegenerative disease: a review of upstream and downstream antioxidant therapeutic options. CurrNeuropharmacol2009;7:65–74. https://doi.org/10.2174/157015909787602823.Search in Google Scholar PubMed PubMed Central

51. Karikas, GA. Chemoprevention, molecular and biochemical mechanisms involved in cancer control and management. Health Sci J2011;5:149–54.Search in Google Scholar

52. Nandakumar, V, Singh, T, Katiya, SK. Multitargeted prevention and therapy of cancer by proanthocyanidins. Cancer Lett2008;269:378–87. https://doi.org/10.1016/j.canlet.2008.03.049.Search in Google Scholar PubMed PubMed Central

53. Su, CC, Chen, GW, Lin, JG, Wu, LT, Chung, JG. Curcumin inhibits cell migration of human colon cancer colo25 cells through the inhibition of nuclear factor kappa B/p65 and down regulates cyclooxygenase-2 and matrix metalloproteinase-2 expressions. Anticancer Res2006;26:1281–8.Search in Google Scholar

54. Vauzour, D, Rodriguez-Mateos, A, Corona, G, Oruna-Concha, MJ. Spencer JPE: polyphenols and human health: preventionof diseases and mechanisms of action. J Nutrients2010;2:1106–31. https://doi.org/10.3390/nu2111106.Search in Google Scholar PubMed PubMed Central

55. Bose, S, Panda, AK, Mukherjee, S, Sa, G. Curcumin and tumor immune-editing: resurrecting the immune system. Cell Div2015;10:6. https://doi.org/10.1186/s13008-015-0012-z.Search in Google Scholar PubMed PubMed Central

56. Yang, Y, Paik, JH, Cho, D, Cho, J, Kim, C. Resveratrol induces the suppression of tumor-derived CD4+ CD25+ regulatory T cells. IntImmunopharm2008;8:542–7. https://doi.org/10.1016/j.intimp.2007.12.006.Search in Google Scholar PubMed

57. Calabrese, V, Bates, TE, Mancuso, C, Cornelius, C, Ventimiglia, B, Cambria, MT, et al.. Curcumin and the cellular stress response in free radical-related diseases. MolNutr Food Res2008;52:1062–73. https://doi.org/10.1002/mnfr.200700316.Search in Google Scholar PubMed

58. Mahassni, SH, Al-Reemi, RM. Apoptosis and necrosis of human breast cancer cells by an aqueous extract of garden cress (Lepidiumsarivum) seeds. Saudi J BiolSci2013;20:131–9. https://doi.org/10.1016/j.sjbs.2012.12.002.Search in Google Scholar PubMed PubMed Central

59. Hasanzadeh, E, Rezazadeh, SH, Shamsa, SF, Dolatabadi, R, Zarringhalam, J. Review on phytochemistry and therapeutic properties of fenugreek (Trigonellafoenum-graceum). J Med Plants2010;2:1–18.Search in Google Scholar

60. Konrad, L, Müller, HH, Lenz, C, Laubinger, H, Aumüller, G, Lichius, JJ. Antiproliferative effect on human prostate cancer cells by a stinging nettle root (Urticadioica) extract. Planta Med2000;66:44–7. https://doi.org/10.1055/s-2000-11117.Search in Google Scholar PubMed

61. Aba, PE, Asuzu, IU, Odo, RI. Antihyperglycaemic and antioxidant potentials of Cussoniaarborea in alloxan-induced diabetic rats.J Comp ClinPathol2012;23:451–8. https://doi.org/10.1007/s00580-012-1640-1.Search in Google Scholar

62. Odo, RI, Asuzu, IU, Aba, PE. The antidiabetic activities of the methanolic root bark extract of Afzelia Africana in alloxan-induced diabetic mice. J ComplIntegr Med2012;9:1553–3840. https://doi.org/10.1515/1553-3840.1649.Search in Google Scholar PubMed

63. Aba, PE, Okenwa-Ani, CP. Biochemical effects of methanolic extracts of Vernoniaamygdalina and Gongronemalatifolia on alloxan-induced diabetic rats. BrJ Pharmaceut Res2016;9:1–10. https://doi.org/10.9734/bjpr/2016/22122.Search in Google Scholar

64. Aba, PE, Ugwueze, KO, Onoja, SO, Okorie-Kanu, CO, Anaga, AO. Hepatoprotective and antioxidant properties of methanol leaf extract of Diaphananthebidens in acetaminophen-induced hepatotoxicity in rats. TropJ Pharmaceut Res2019;18:2371–7.Search in Google Scholar

65. Swem, TF, Aba, PE, Udem, SC. Ameliorative effect and in vivo antioxidant properties of methanol extract of Burkea Africana stem bark on acetaminophen-induced hepatotoxicity in rats. TropJ Natur Prod Res2020;4:36–42. https://doi.org/10.26538/tjnpr/v4i2.3.Search in Google Scholar

66. Hoeijmakers, JHJ. DNA damage, aging, and cancer.N Engl J Med2009;361:1475–85. https://doi.org/10.1056/nejmra0804615.Search in Google Scholar

67. Gavande, NS, Vandervere-Carroza, PS, Hinshaw, HD, Jalal, SI, Sears, CR, Pawelczak, KS, et al.. DNA repair targeted therapy: the past or future of cancer treatment?PharmacolTherapeut2016;160:65–83. https://doi.org/10.1016/j.pharmthera.2016.02.003.Search in Google Scholar PubMed PubMed Central

68. Ciccia, A, Elledge, SJ. The DNA damage response: making it safe to play with knives. Mol Cell2010;40:179–204. https://doi.org/10.1016/j.molcel.2010.09.019.Search in Google Scholar PubMed PubMed Central

69. Kelley, MR, Logsdon, D, Fishel, ML. Targetting DNA repair pathways for cancer treatment: what’s new?Future Oncol2014;10:1215–37. https://doi.org/10.2217/fon.14.60.Search in Google Scholar PubMed PubMed Central

70. Hofbauer, R, Frass, M, Gmeiner, B, Kaye, AD, Frost, EA. Effects of Ferula assa-foetida extract on neutrophil migration at the cellular level. Heart Dis2001;3:14–7. https://doi.org/10.1097/00132580-200101000-00003.Search in Google Scholar PubMed

71. Byrd, JC, Lin, TS, Dalton, JT, Wu, D, Phelps, MA, Fisher, B, et al.. Flavopiridol administered using a pharmacologically derived schedule is associated with marked clinical efficacy in refractory, genetically high-risk chronic lymphocytic leukemia. Blood2007;109:399–404. https://doi.org/10.1182/blood-2006-05-020735.Search in Google Scholar PubMed PubMed Central

72. Visconti, R, Della, R, Grieco, D. Cell cycle check point in cancer: a therapeutically targeted double-edged sword. J ExpClin Cancer Res2016;35:153. https://doi.org/10.1186/s13046-016-0433-9.Search in Google Scholar PubMed PubMed Central

73. Dickson, MA, Schwartz, GK. Development of cell-cycle inhibitors for cancer therapy.CurrOncol2009;16:36–43. https://doi.org/10.3747/co.v16i2.428.Search in Google Scholar PubMed PubMed Central

74. Sutherland, RL, Musgrove, EA. Cyclin D and mammary carcinoma. New insights from transgenic mouse models.Breast Cancer Res2002;4:14–7. https://doi.org/10.1186/bcr411.Search in Google Scholar PubMed PubMed Central

75. Chen, YN, Sharma, SK, Ramsey, TM, Jiang, L, Martin, MS, Baker, K, et al.. Selective killing of transformed cells by cyclin/cyclin-dependent kinase-2 antagonists. Proc Natl AcadSci USA1999;96:4325–9. https://doi.org/10.1073/pnas.96.8.4325.Search in Google Scholar PubMed PubMed Central

76. Sherr, CJ. G1 phase progression: cycling on cue. Cell1994;79:551–5. https://doi.org/10.1016/0092-8674(94)90540-1.Search in Google Scholar PubMed

77. Zhou, J, Glannakakou, P. Targeting microtubule for cancer chemotherapy. Curr Med ChemAnti Cancer Agents2005;5:65–71. https://doi.org/10.2174/1568011053352569.Search in Google Scholar PubMed

78. Ayyad, SEN, Abdel-Lateff, A, Alarif, WM, Patacchioli, FR, Badria, FA, Ezmirly, ST. In vitro and in vivo study of cucurbitacins-type triterpene glucoside from Citrulluscolocynthis growing in Saudi Arabia against hepatocellular carcinoma.Environ ToxicolPharmacol2012;33:245–51. https://doi.org/10.1016/j.etap.2011.12.010.Search in Google Scholar PubMed

79. TavakkolAfshari, J, Rakhshandeh, H, Zamani, AR, MahdaviShahri, N, Ghazezadeh, L, Norozi, M. Cytotoxicity effects of Citrulluscolocynthis on Hep2 and L929 cell lines. Hakim Res J2005;8:47–54.Search in Google Scholar

80. Gupta, GP, Massagué, J. Cancer metastasis: building a framework. Cell2006;17127:679–95. https://doi.org/10.1016/j.cell.2006.11.001.Search in Google Scholar PubMed

81. Buchheit, CL, Weigel, KJ, Schafer, ZT. Cancer cell survival during detachment from the ECM: multiple barriers to tumour progression. Nat Rev Cancer2014;14:632–41. https://doi.org/10.1038/nrc3789.Search in Google Scholar PubMed

82. Fontebasso, Y, Dubinett, SM. Drug development for metastasis prevention. Crit Rev Oncog2015;20:449–73. https://doi.org/10.1615/CritRevOncog.v20.i5-6.150.Search in Google Scholar PubMed PubMed Central

83. Sennino, B, Ishiguro-Oonuma, T, Wei, Y, Naylor, RM, Williamson, CW, Bhagwandin, V, et al.. Suppression of tumor invasion and metastasis by concurrent inhibition of c-Met and VEGF signaling in pancreatic neuroendocrine tumors. Cancer Discov 2012;2:270–87. https://doi.org/10.1158/2159-8290.cd-11-0240.Search in Google Scholar PubMed PubMed Central

84. Alizadeh, AM, Shiri, S, Farsinejad, S. Metastasis review: from bench to bedside. Tumour Biol2014;35:8483–523. https://doi.org/10.1007/s13277-014-2421-z.Search in Google Scholar PubMed

85. Wolf, K, Mazo, I, Leung, H, Engelke, K, Von Andria, UH, Deryugina, EI, et al.. Compensation mechanism in tumor cell migration: mesenchymal-amoeboid transition after blocking of pericellular proteolysis. J Cell Biol2003;160:267–77. https://doi.org/10.1083/jcb.200209006.Search in Google Scholar PubMed PubMed Central

86. Van Goietsenoven, G. In vitro growth inhibitory effects of cytochalasins and derivatives in cancer cells.Planta Med2011;77:711–7. https://doi.org/10.1055/s-0030-1250523.Search in Google Scholar PubMed

87. Schwab, A, Stock, C. Ion channels and transporters in tumour cell migration and invasion. Philos Trans R SocLond B BiolSci2014;369:20130102. https://doi.org/10.1098/rstb.2013.0102.Search in Google Scholar PubMed PubMed Central

88. Sarkar, FH, Li, Y, Wang, Z, Padhye, S. Lesson learned from nature for the development of novel anti-cancer agents: implication of isoflavone, curcumin, and their synthetic analogs. CurrPharmaceut Des2010;16:1801–12. https://doi.org/10.2174/138161210791208956.Search in Google Scholar PubMed PubMed Central

89. de Bono, JS, Tolcher, AW, Rowinsky, EK.The future of cytotoxic therapy: selective cytotoxicity based on biology is the key. Breast Cancer Res2003;5:154–9. https://doi.org/10.1186/bcr597.Search in Google Scholar PubMed PubMed Central

90. Prakash, V. Terpenoidsascytotoxic compounds: a perspective. Pharmacogn Rev2018;12:166–76. https://doi.org/10.4103/phrev.phrev_3_18.Search in Google Scholar

91. Agarwal, G, Carcache, PB, Addo, EM, Kinghorn, AD. Current status and contemporary approaches to the discovery of antitumor agents from higher plants. Biotechnol Adv 2020;38:107337.10.1016/j.biotechadv.2019.01.004Search in Google Scholar PubMed PubMed Central

92. Erasto, P, Viljoen, A. Limonene—a review: biosynthetic, ecological and pharmacological relevance. NatProd Comm2008;3:1193–9. https://doi.org/10.1177/1934578x0800300728.Search in Google Scholar

93. Malko, MW, Wróblewska, A, Chemical, O. The importance of R-(+)-limonene as the raw material for organic syntheses and for organic industry.Chemik2016;70:193–202.Search in Google Scholar

94. Jia, S, Xi, G, Zhang, M, Chen, Y, Lei, BO, Dong, X, et al.. Induction of apoptosis by D-limonene is mediated by inactivation of Akt in LS174T human colon cancer cells. OncolRep2013;3:349–54. https://doi.org/10.3892/or.2012.2093.Search in Google Scholar PubMed

95. Yang, C, Chen, H, Chen, H, Zhong, B, Luo, X, Chun, J. Antioxidant and anticancer activities of essential oil from gannan navel orange peel. Molecules2017;22:1–10. https://doi.org/10.3390/molecules22081391.Search in Google Scholar PubMed PubMed Central

96. Ren, G, Shi, Z, Cong, T, Yao, Y. Antiproliferative activity of combined Biochanin A and GinsenosideRh2 on MDA-MB-231 and MCF-7 human breast cancer cells. Molecules2018;23:1–14. https://doi.org/10.3390/molecules23112908.Search in Google Scholar PubMed PubMed Central

97. Sheihet, L, Garbuzenko, OB, Bushman, J, Gounder, MK, Minko, T, Kohn, J. Paclitaxel in tyrosine-derived nanospheres as a potential anti-cancer agent: in vivo evaluation of toxicity and efficacy in comparison with paclitaxel in cremophor. Eur J PharmaceutSci2012;45:320–9. https://doi.org/10.1016/j.ejps.2011.11.017.Search in Google Scholar PubMed PubMed Central

98. Pozo-Guisado, E, Centeno, F, Merino, JM, Mulero-navarro, S, Jesu, M, Alvarez-barrientos, A, et al.. Resveratrol-induced apoptosis in MCF-7 human breast cancer cells involves a caspase-independent mechanism with downregulation of Bcl-2 and NF-kB. Int J Cancer2005;115:74–84. https://doi.org/10.1002/ijc.20856.Search in Google Scholar PubMed

99. Kim, KH, Seo, HS, Choi, HS, Choi, I, Shin, YC, Ko, S. Induction of apoptotic cell death by ursolic acid through mitochondrial death pathway and extrinsic death receptor pathway in MDA-MB-231 cells.Arch Pharm Res2011;34:1363–72. https://doi.org/10.1007/s12272-011-0817-5.Search in Google Scholar PubMed

100. Lou, C, Yokoyama, S, Saiki, I, Hayakawa, Y. Selective anticancer activity of hirsutine against HER2positive breast cancer cells by inducing DNA damage. Oncol Rep2015;33:2072–6. https://doi.org/10.3892/or.2015.3796.Search in Google Scholar PubMed

101. Wang, XD, Li, CY, Jiang, MM, Li, D, Wen, P, Song, X, et al.. Induction of apoptosis in human leukemia cells through an intrinsic pathway by cathachunine, a unique alkaloid isolated from Catharanthusroseus. Phytomedicine2016;23:641–53. https://doi.org/10.1016/j.phymed.2016.03.003.Search in Google Scholar PubMed

102. Liew, SY, Looi, CY, Paydar, M, Cheah, FK, Leong, KH, Wong, WF, et al.. Subditine, a new monoterpenoid indole alkaloid from bark of Naucleasubdita (Korth.) Steud.Induces apoptosis in human prostate cancer cells.PLoSOne2014;9:e87286. https://doi.org/10.1371/journal.pone.0087286.Search in Google Scholar PubMed PubMed Central

103. Lee, ST, Wong, PF, Cheah, SC. Alpha-tomatine induces apoptosis and inhibits nuclear factor-kappa B activation on human prostatic adenocarcinoma PC-3 cells. PLoSOne2011;6:e18915. https://doi.org/10.1371/journal.pone.0018915.Search in Google Scholar PubMed PubMed Central

104. Gonzalez, VM, Fuertes, MA, Alonso, C, Perez, JM.Is cisplatin-induced cell death always produced by apoptosis?MolPharmacol2001;59:657–63. https://doi.org/10.1124/mol.59.4.657.Search in Google Scholar PubMed

105. Al-Snafi, AE. Chemical constituents and pharmacological activities of Ammi majus and Ammi visnaga—a review.Int J Pharm Ind Res2013;3:257–65.Search in Google Scholar

106. Nemati, F, EslamiJadidi, B, TalebiDarabi, M. Investigation cytotoxic effects of Ammi maju extract on MCF-7and HeLa cancer cell line. J AnimBiol2013;5:59–66.Search in Google Scholar

107. Shokoohinia, Y, Hosseinzadeh, L, Alipour, M, Mostafaie, A, Mohammadi-Motlagh, HR. Comparative evaluation of cytotoxic and apoptogenic effects of several coumarins on human cancer cell lines: osthole induces apoptosis in p53-deficient H1299 cells. Adv Pharmacol Sci 2014;2014:847574. https://doi.org/10.1155/2014/847574.Search in Google Scholar PubMed PubMed Central

108. MomtaziBorojeni, A, Behbahani, M, Sadeghi-Aliabadi, H. Evaluation of cytotoxic effect of some extracts of Avicennia marina against MDA-MB231 human breast cancer cell line. PharmaceutSci2011;16:229–38.Search in Google Scholar

109. Sharaf, M, El-Ansari, MA, Saleh, NA. New flavonoids from Avicennia marina.Fitoterapia2000;71:274–7. https://doi.org/10.1016/s0367-326x(99)00169-0.Search in Google Scholar PubMed

110. Androutsopoulos, VP, Tsatsakis, AM, Spandidos, DA. Cytochrome P450CYP1A1: wider roles in cancer progression and prevention. BMC Cancer 2009;9:187. https://doi.org/10.1186/1471-2407-9-187.Search in Google Scholar PubMed PubMed Central

111. Buterin, T, Hess, MT, Luneva, N, Geacintov, NE, Amin, S, Kroth, H, et al.. Unrepaired fjord region polycyclic aromatic hydrocarbon-DNA adducts in ras codon 61 mutational hot spots. Cancer Res2000;60:1849–56.Search in Google Scholar

112. Guengerich, FP, Shimada, T. Oxidation of toxic and carcinogenic chemicals by human cytochrome P450 enzymes. Chem Res Toxicol1991;4:391–407. https://doi.org/10.1021/tx00022a001.Search in Google Scholar PubMed

113. Deonarain, MP, Epenetos, AA. Targeting enzymes for cancer therapy: old enzymes in new roles.Br J Cancer1994;70:786–94. https://doi.org/10.1038/bjc.1994.400.Search in Google Scholar PubMed PubMed Central

114. Senter, PD, Saulnier, MG, Schreiber, GJ, Hirschiberg, DL, Brown, JP, Hellstrom, I, et al.. Antitumour effects of antibody-alkaline phosphatase conjugates in combination with etoposide phosphate. Proc Natl AcadSci USA1988;85:4842–6. https://doi.org/10.1073/pnas.85.13.4842.Search in Google Scholar PubMed PubMed Central

115. Rowlinson-Busza, G, Bamias, A, Kraus, T, Epenetos, AA. Antibody-guided nitrile therapy (AGENT).In vivo cytotoxicity and in vitro tumour localization. In: Epenetos, AA, editor. Monoclonal antibodies: applications in clinical oncology. London: Chapman & Hall; 1992:111–8pp.Search in Google Scholar

116. Rajavel, T, Packiyaraj, P, Suryanarayana, V, Singh, SK, Ruchmani, K, Devi, KP. βsitosterol targets Trx/Trx1 reductase to induce apoptosis in A549 cells via ROS mediated mitochondrial dysregulation and p53 activation. SciRep2018;8:1–15. https://doi.org/10.1038/s41598-018-20311-6.Search in Google Scholar PubMed PubMed Central

Received: 2021-08-25
Accepted: 2021-11-28
Published Online: 2021-12-16

© 2021 Walter de Gruyter GmbH, Berlin/Boston

Articles in the same Issue

  1. Frontmatter
  2. Minireview
  3. Impact of mental toughness on athlete’s performance and interventions to improve
  4. Reviews
  5. A review of the mechanisms of anti-cancer activities of some medicinal plants–biochemical perspectives
  6. Antimicrobials in COVID-19: strategies for treating a COVID-19 pandemic
  7. Anxiolytic effects of vestibular stimulation: an update
  8. Original Articles
  9. Intermittent exposure to green and white light-at-night activates hepatic glycogenolytic and gluconeogenetic activities in male Wistar rats
  10. Study of pre-operative neutrophil–lymphocyte ratio in urothelial carcinoma
  11. The effects of Berberis vulgaris L. root extract on the opiate withdrawal syndrome and psychological factors: a randomized double-blind clinical trial
  12. Evidence of alterations in the learning and memory in offspring of stress-induced male rats
  13. The impact of vestibular symptoms and electronystagmography results on recovery from sudden sensorineural hearing loss
  14. Complementary mechanisms of modulation of spontaneous phasic contractions by the gaseous signalling molecules NO, H2S, HNO and the polysulfide Na2S3 in the rat colon
  15. Pharmacist-directed Sputnik V (GAM-COVID-VAC) surveillance program: a prospective observational study in Southern India
  16. Correlation among Poincare plot and traditional heart rate variability indices in adults with different risk levels of metabolic syndrome: a cross-sectional approach from Southern India
  17. Does etodolac affect TRPA1 functionality in vivo in human?
  18. Dynamic of irisin secretion change after moderate-intensity chronic physical exercise on obese female
  19. Letter to the Editor
  20. The prospective record-breaking obesity drug tirzepatide raises concerns about affordability
Downloaded on 25.9.2025 from https://www.degruyterbrill.com/document/doi/10.1515/jbcpp-2021-0257/html
Scroll to top button