Assessment of Cytotoxic Effect and Phytoconstituents of Moringa oleifera Seeds Cultivated in Iraq Against MCF-7 Breast Cancer Cells

Document Type : Research Paper

Authors

Pharmacognosy and Medicinal Plants Department, Pharmacy College, Baghdad University, Baghdad, Iraq

Abstract

The cytotoxic activity of Moringa oleifera (MO) dried seeds against the Michigan Cancer Foundation-7 (MCF-7) cell line was assessed, and its phytoconstituents were screened by reverse-phase high-performance liquid chromatography (RP-HPLC). For this purpose, butanol and ethyl acetate extracts of MO seeds were prepared, and the 3-(4,5-dimethylthiazoline-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay was performed on MCF-7 breast cancer cells treated with different concentrations of the ethyl acetate extract (31.25, 62.5, 125, 250, 500, and 1000 µg/ml). After 72 hours of treatment, cell viability was assessed. The ethyl acetate fraction of MO seeds showed cytotoxic activity with a half-maximal inhibitory concentration (IC50) value of 60 µg/ml against the MCF-7 cell line. In addition, RP-HPLC analysis showed that caffeic acid, ellagic acid and p-coumaric acid were found in abundance in the butanol fraction, while ferulic acid was found in abundance in the ethyl acetate fraction. Overall, extracts from MO seeds show potential anticancer activity.

Keywords

Main Subjects


  1. Mbikay M. Therapeutic potential of Moringa oleifera leaves in chronic hyperglycemia and dyslipidemia: A review. Frontiers in Pharmacology. 2012;3:24.

    1. Leone A., Spada A., Battezzati A., Schiraldi A., Aristil J., Bertoli S. Moringa oleifera seeds and oil: Characteristics and uses for human health. International Journal of Molecular Sciences. 2016;17(12):2141.
    2. Popoola J.O., Obembe O.O. Local knowledge, use pattern and geographical distribution of Moringa oleifera Lam. (Moringaceae) in Nigeria. Journal of Ethnopharmacology. 2013;150(2):682-691.
    3. Garcia T.B., Soares A.A., Costa J.H., Costa H.P., Neto J.X., Rocha-Bezerra L.C., Silva F.D., Arantes M.R., Sousa D.O., Vasconcelos I.M., Oliveira J.T. Gene expression and spatiotemporal localization of antifungal chitin-binding proteins during Moringa oleifera seed development and germination. Planta. 2019;249:1503-1519.
    4. Kadhim E.J., AL-Shammaa D.A. Phytochemical characterization using GC-MS analysis of methanolic extract of Moringa oleifera (Family Moringaceae) plant cultivated in Iraq. Chemistry and Materials Research. 2014;6(5):9-26.
    5. Gupta R., Dubey D.K., Kannan G.M., Flora S.J. Concomitant administration of Moringa oleifera seed powder in the remediation of arsenic‐induced oxidative stress in mouse. Cell Biology International. 2007;31(1):44-56.
    6. Berkovich L., Earon G., Ron I., Rimmon A., Vexler A., Lev-Ari S. Moringa Oleifera aqueous leaf extract down-regulates nuclear factor-kappaB and increases cytotoxic effect of chemotherapy in pancreatic cancer cells. BMC Complementary and Alternative Medicine. 2013;13:212.

    83

    1. Xie J., Luo F.X., Shi C.Y., Jiang W.W., Qian Y.Y., Yang M.R., Song S., Dai T.Y., Peng L., Gao X.Y., Tao L. Moringa oleifera alkaloids inhibited PC3 cells growth and migration through the COX-2 mediated wnt/β-catenin signaling pathway. Frontiers in Pharmacology. 2020;11:523962.
    2. Do B.H., Hoang N.S., Nguyen T.P., Ho N.Q., Le T.L., Doan C.C. Phenolic extraction of Moringa oleifera leaves induces caspase-dependent and caspase-independent apoptosis through the generation of reactive oxygen species and the activation of intrinsic mitochondrial pathway in human melanoma cells. Nutrition and Cancer. 2021;73(5):869-888.
    3. Tan H.W., Mo H.Y., Lau A.T., Xu Y.M. Selenium species: Current status and potentials in cancer prevention and therapy. International Journal of Molecular Sciences. 2018;20(1):75.
    4. Wu X., Zhou Q.H., Xu K. Are isothiocyanates potential anti-cancer drugs?. Acta Pharmacologica Sinica. 2009;30(5):501-512.
    5. Lopez-Rodriguez N.A., Gaytán-Martínez M., de la Luz Reyes-Vega M., Loarca-Piña G. Glucosinolates and isothiocyanates from Moringa oleifera: Chemical and biological approaches. Plant Foods for Human Nutrition. 2020;75:447-457.
    6. Wang X., Liu Y., Liu X., Lin Y., Zheng X., Lu Y. Hydrogen sulfide (H2S) releasing capacity of isothiocyanates from Moringa oleifera Lam. Molecules. 2018;23(11):2809.
    7. Jaja-Chimedza A., Zhang L., Wolff K., Graf B.L., Kuhn P., Moskal K., Carmouche R., Newman S., Salbaum J.M., Raskin I. A dietary isothiocyanate-enriched Moringa (Moringa oleifera) seed extract improves glucose tolerance in a high-fat-diet mouse model and modulates the gut microbiome. Journal of Functional Foods. 2018;47:376-385.
    8. Park E.J., Cheenpracha S., Chang L.C., Kondratyuk T.P., Pezzuto J.M. Inhibition of lipopolysaccharide-induced cyclooxygenase-2 and inducible nitric oxide synthase expression by 4-[(2′-O-acetyl-α-L-rhamnosyloxy) benzyl] isothiocyanate from Moringa oleifera. Nutrition and Cancer. 2011;63(6):971-982.
    9. Bedewi B.K., Jasim G.A., Abbas I.S., Al-Sudani B. Cytotoxicity of cryptochlorogenic acid against breast cancer cell line (MCF7) isolated from Moringa oleifera leaves cultivated in Iraq. Al-Mustansiriyah Journal of Pharmaceutical Sciences. 2022;22(2):35-43.
    10. Hussein A.M., Kadum E.J. Identification and isolation of caffeic, chlorogenic and ferulic acids in aerial parts of Capparis spinosa wildly grown in Iraq. Iraqi Journal of Pharmaceutical Sciences. 2020;29(2):185-193.
    11. Al-Shammari A.M., Alshami M.A., Umran M.A., Almukhtar A.A., Yaseen N.Y., Raad K., Hussien A.A. Establishment and characterization of a receptor-negative, hormone-nonresponsive breast cancer cell line from an Iraqi patient. Breast Cancer: Targets and Therapy. 2015:223-230.
    12. Adil B.H., Al-Shammari A.M., Murbat H.H. Breast cancer treatment using cold atmospheric plasma generated by the FE-DBD scheme. Clinical Plasma Medicine. 2020;19:100103.
    13. Abdullah S.A., Al-Shammari A.M., Lateef S.A. Attenuated measles vaccine strain have potent oncolytic activity against Iraqi patient derived breast cancer cell line. Saudi Journal of Biological Sciences. 2020;27(3):865-872.
    14. Al-Shammari A.M., Jalill R.D., Hussein M.F. Combined therapy of oncolytic Newcastle disease virus and rhizomes extract of Rheum ribes enhances cancer virotherapy in vitro and in vivo. Molecular Biology Reports. 2020;47(3):1691-1702.
    15. Mohammed M.S., Al-Taee M.F., Al-Shammari A.M. Caspase dependent and independent anti-hematological malignancy activity of AMHA1 attenuated newcastle disease virus. International Journal of Molecular and Cellular Medicine. 2019;8(3):211.
    16. Al-Ziaydi A.G., Al-Shammari A.M., Hamzah M.I., Kadhim H.S., Jabir M.S. Newcastle disease virus suppress glycolysis pathway and induce breast cancer cells death. Virusdisease. 2020;31(3):341-348.
    17. Brilhante R.S., Sales J.A., Pereira V.S., Castelo D.D., de Aguiar Cordeiro R., de Souza Sampaio C.M., Paiva M.D., Dos Santos J.B.,

    84

    Sidrim J.J., Rocha M.F. Research advances on the multiple uses of Moringa oleifera: A sustainable alternative for socially neglected population. Asian Pacific Journal of Tropical Medicine. 2017;10(7):621-630.

    1. Guevara A.P., Vargas C., Sakurai H., Fujiwara Y., Hashimoto K., Maoka T., Kozuka M., Ito Y., Tokuda H., Nishino H. An antitumor promoter from Moringa oleifera Lam. Mutation Research/Genetic Toxicology and Environmental Mutagenesis. 1999;440(2):181-188.
    2. Dai J., Mumper R.J. Plant phenolics: Extraction, analysis and their antioxidant and anticancer properties. Molecules. 2010;15(10):7313-7352.
    3. Munday R., Munday C.M. Induction of phase II detoxification enzymes in rats by plant-derived isothiocyanates: comparison of allyl isothiocyanate with sulforaphane and related compounds. Journal of Agricultural and Food Chemistry. 2004;52(7):1867-1871.
    4. Kou X., Kirberger M., Yang Y., Chen N. Natural products for cancer prevention associated with Nrf2–ARE pathway. Food Science and Human Wellness. 2013;2(1):22-28.
    5. Słoczyńska K., Powroźnik B., Pękala E., Waszkielewicz A.M. Antimutagenic compounds and their possible mechanisms of action. Journal of Applied Genetics. 2014;55:273-285.