The effect of Phyllanthus niruri L extracts on human leukemic cell proliferation and apoptosis induction
Abstract
Objective: To investigate the effect of Phyllanthus niruri Linn (Euphorbiaceae) in the proliferation of human leukemic cells (MOLT-4 and K562).
Methods: Phyllanthus niruri L (P.niruri) was macerated by using various solvents to obtain the crude extracts. Cytotoxicity of the extracts against MOLT-4 and K562 cells was tested using MTT assay to find the IC50 value. To analyse cell cycle progression, cellular DNA was measured using propidium iodide (PI) staining. Apoptosis induction was evaluated using Annexin V-FITC and PI staining and analysed using FACSVerse flow cytometry. Finally, the expression of p53 on MOLT-4 and K562 cell lysate was measured by western blotting, to identify the possible mode of action of the anticancer activity.
Results: P. niruri crude extracts demonstrated a potential anti-cancer effect towards MOLT-4 cells (IC50 range was 42.21 ± 4.98 to 97.06 ± 18.29 µg/ml). However, against K562 cells, P.niruri extracts exhibited a lower inhibitory potency (the IC50 was 120.19 ± 8.48 to 256.55 ± 26.22 µg/ml). The results showed the selectivity of the toxic effect of the extracts against MOLT-4 and K562. To evaluate the possible mechanism of action the anticancer effect, we evaluated P. niruri extract action in apoptosis induction and p53 expression. The results showed that methanol and hexane extract inhibited MOLT-4 cell progression from G1 to S-phase, indicating G1 cell arrest. Moreover, apoptotic cell population following treatment of MOLT-4 and K562 cells with methanol extract was markedly increased, showing morphological signs of apoptosis including membrane degradation and chromatin condensation. Furthermore, we found that there was an increase in p53 expression following MOLT-4 treatment with methanol extract, suggesting that p53 induction may be involved in cell apoptosis.
Conclusions: The results indicated the involvement of p53 pathway in the mechanism of anti-cancer activity exerted by P. niruri extract on MOLT-4 cells. However, for cancer cells lacking P53 expression, such as K562 cells, apoptosis might take place via other pathways.
Keywords
Full Text:
PDFReferences
Horner M, Ries L, Krapcho M, Neyman N, Aminou R, Howlader N, Altekruse S, Feuer E, Huang L, Mariotto A. SEER Cancer Statistics Review, 1975-2006. National Cancer Institute 2009 [cited 2018 Jan 15]. Available from: https://seer.cancer.gov/archive/csr/1975_2006/index.html
Zeidan AM, Mahmoud D, Kucmin-Bemelmans IT, Alleman CJ, Hensen M. Skikne B, Smith BD. Economic burden associated with acute myeloid leukemia treatment. Expert review of hematology 2016; 9:79-89.
Tang YQ, Jaganath IB, Sekaran SD. Phyllanthus spp. induces selective growth inhibition of PC-3 and MeWo human cancer cells through modulation of cell cycle and induction of apoptosis. PloS one 2010; 5: e12644.
Nobili S, Lippi D, Witort E, Donnini M, Bausi L, Mini E, Capaccioli S. Natural compounds for cancer treatment and prevention. Pharmacological Research 2009; 59:365-78.
Newman DJ, Cragg GM. Natural Products as Sources of New Drugs over the Last 25 Years. Journal of natural products 2007;70:461-77.
Puspita N. Isolation and characterisation of medicinal compounds from Phyllanthus Niruri L, in Environment and life science. 2015, University of Salford.
Sabir S, Rocha J. Water-extractable phytochemicals from Phyllanthus niruri exhibit distinct in vitro antioxidant and in vivo hepatoprotective activity against paracetamol-induced liver damage in mice. Food Chemistry 2008; 111:845-51.
Bagalkotkar G, Sagineedu S, Saad M, Stanslas J. Phytochemicals from Phyllanthus niruri Linn and their pharmacological properties: a review. Journal of pharmacy and pharmacology 2006;58:1559-70.
Iizuka T, Nagai M, Taniguchi A, Moriyama H, Hoshi K. Inhibitory effects of methyl brevifolincarboxylate isolated from Phyllanthus niruri L on platelet aggregation. Biological & pharmaceutical bulletin 2007;30: 382-4.
Syamasundar KV, Singh B, Singh Thakur R, Husain A, Yoshinobu K, Hiroshi H. Antihepatotoxic principles of Phyllanthus niruri herbs. Journal of ethnopharmacology 1985;14: 41-4.
Than N, Fotso S, Poeggeler B, Hardeland R, Laatsch H. Niruriflavone, a new antioxidant flavone sulfonic acid from Phyllanthus niruri. Zeitschrift Fur Naturforschung B 2006;61:57.
Sahni S, Maurya S, Singh U, Singh A, Singh V, Pandey V. Antifungal activity of nor-securinine against some phytopathogenic fungi. Mycobiology 2005; 33:97-103.
Lee TJ, Kim OH, Kim YH, Lim JH, Kim S, Park JW, Kwon TK. Quercetin arrests G2/M phase and induces caspase-dependent cell death in U937 cells. Cancer Letters 2006:240:234-42.
De Araújo Júnior RF, De Souza TP, Pires JGL, Soares LAL, De Araújo AA, Petrovick PR, Mâcedo HDO, De Sá Leitão ALC, Guerra GCB. A dry extract of Phyllanthus niruri protects normal cells and induces apoptosis in human liver carcinoma cells. Experimental Biology and Medicine 2012;237:1281-8.
Huang ST, Yang RC, Chen MY, Pang JHS. Phyllanthus urinaria induces the Fas receptor/ligand expression and ceramide-mediated apoptosis in HL-60 cells. Life Sciences 2004;75:339-51.
Pettit R, Schaufelberger DE, Nieman RA, Dufresne C, Saenz-Renauld JA. Antineoplastic agents, 1771 isolation and structure of phyllanthostatin 6. Journal of Natural Products 1990;53:1406-13.
Harikumar KB, Kuttan G, Kuttan R. Phyllanthus amarus inhibits cell growth and induces apoptosis in Dalton's lymphoma ascites cells through activation of caspase-3 and downregulation of Bcl-2. Integr Cancer Ther 2009;8:190-4.
Schneider CA, Rasband WS, Eliceiri KW. Nih Image to ImageJ: 25 years of image analysis. Nat Meth 2012;9:671-5.
Ma XC, Liu CY, Sun XJ, He JJ, Wan SG, Sun WL. Genetic characteristics of human acute lymphoblastic leukemia cell line Molt-4. Zhongguo Shi Yan Xue Ye Xue Za Zhi 2014;22:280-4.
Hofseth LJ, Hussain SP, Harris CC p53: 25 years after its discovery. Trends in Pharmacological Sciences 2004;25:177-81.
Newman DJ, Cragg GM. Natural Products As Sources of New Drugs over the 30 Years from 1981 to 2010. Journal of Natural Products 2012;75:311-35.
Xiao Z, Morris‐Natschke SL, Lee KH. Strategies for the optimization of natural leads to anticancer drugs or drug candidates. Medicinal research reviews 2016;36:32-91.
Shoeb M. Anticancer agents from medicinal plants. Bangladesh journal of pharmacology 2006;1:35-41.
Cragg GM, Newman DJ. Plants as a source of anti-cancer agents. Journal of Ethnopharmacology 2005;100:72-9.
Samali A, Florence D, Odeniran O, Cordelia O. Evaluation of chemical constituents of Phyllanthus Niruri. African Journal of Pharmacy and Pharmacology 2012;6:125-8.
Fresco P, Borges F, Diniz C, Marques M. New insights on the anticancer properties of dietary polyphenols. Medicinal research reviews 2006;26:747-66.
Huang ST, Pang JHS, Yang RC. Anti-cancer Effects of Phyllanthus urinaria and Relevant Mechanisms. Chang Gung Medical Journal 2010;33:477-87.
Koeffler H, Golde D. Human myeloid leukemia cell lines: a review. Blood 1980;56:344-50.
Andersson L C, Nilsson K, Gahmberg, CG. K562—a human erythroleukemic cell line. International journal of cancer 1979;23:143-7.
Klein E, Vánky F, Ben‐Bassat H, Neumann H, Ralph P, Zeuthen J, Polliack A. Properties of the K562 cell line, derived from a patient with chronic myeloid leukemia. International journal of cancer 1976;18:421-31.
Sakkrom P, Pompimon W, Meepowpan P, Nuntasaen N, Loetchutinat C. The effect of phyllanthus taxodiifolius beille extracts and its triterpenoids studying on cellular energetic stage of cancer cells. American Journal of Pharmacology and Toxicology 2010;5:139-44.
Evan GI, Vousden KH. Proliferation, cell cycle and apoptosis in cancer. Nature 2001;411:342-8.
Fulda S, Debatin K. Extrinsic versus intrinsic apoptosis pathways in anticancer chemotherapy. Oncogene 2006;25:4798-811.
Brown JM, Wouters BG. Apoptosis, p53, and tumor cell sensitivity to anticancer agents. Cancer research 1999;59:1391-9.
Calixto JB, Santos AR, Cechinel FV, Yunes RA. A review of the plants of the genus Phyllanthus: their chemistry, pharmacology, and therapeutic potential. Medicinal research reviews 1998; 18: 225-58.
Agarwal C, Tyagi A, Agarwal R. Gallic acid causes inactivating phosphorylation of cdc25A/cdc25C-cdc2 via ATM-Chk2 activation, leading to cell cycle arrest, and induces apoptosis in human prostate carcinoma DU145 cells. Mol Cancer Ther2006;5:3294-302.
Lowe SW, Bodis S, Mcclatchey A, Remington L, Ruley HE, Fisher DE, Housman DE, Jacks T. p53 status and the efficacy of cancer therapy in vivo. Science 1994;266:807-10.
Gaidano G, Ballerini P, Gong JZ, Inghirami G, Neri A, Newcomb EW, Magrath IT, Knowles DM, Dalla-Favera R. p53 mutations in human lymphoid malignancies: association with Burkitt lymphoma and chronic lymphocytic leukemia. Proceedings of the National Academy of Sciences 1991;88:5413-17.
Bunz F, Hwang PM, Torrance C, Waldman T, Zhang Y, Dillehay L, Williams J, Lengauer C, Kinzler KW, Vogelstein B. Disruption of p53 in human cancer cells alters the responses to therapeutic agents. The Journal of clinical investigation 1999;104:263-9.
Dasari S, Tchounwou PB. Cisplatin in cancer therapy: molecular mechanisms of action. European journal of pharmacology 2014;0:364-78.
DOI: http://dx.doi.org/10.14499/indonesianjpharm30iss4pp241
Refbacks
- There are currently no refbacks.
Copyright (c) 2019 Indonesian Journal of Pharmacy

This work is licensed under a Creative Commons Attribution-ShareAlike 4.0 International License.
Indonesian J Pharm indexed by: