SYNERGISTIC GROWTH INHIBITORY EFFECT OF FLAVONOL–KAEMPFEROL AND CONVENTIONAL CHEMOTHERAPEUTIC DRUGS ON CANCER CELLS

Authors

  • Chepuri Kalyani Centre for Biotechnology, Institute of Science and Technology, JNTUH, Hyderabad, Telangana 500085, India
  • Mangamoori Lakshmi Narasu Centre for Biotechnology, Institute of Science and Technology, JNTUH, Hyderabad, Telangana 500085, India
  • Yumnum Priyadarshini Devi Dr. Reddy’s Laboratories, Hyderabad, Telangana 500072, India

DOI:

https://doi.org/10.22159/ijpps.2017v9i2.16021

Keywords:

Kaempferol, Doxorubicin, Cisplatin, Combination index, HCT-15, MDA MB 231, Synergism

Abstract

Objective: The objective of the present study was to evaluate synergistic growth inhibitory effect of a flavonol, kaempferol in combination with chemotherapeutic drugs doxorubicin or cisplatin.

Methods: The anti-proliferative activities of kaempferol, doxorubicin and cisplatin on human colorectal cancer cells (HCT-15) and human breast cancer (MDA MB 231) were analyzed by 3-(4,5-dimehylthiaol-2-yl)-2,5-diphenyltetraolium bromide (MTT) assay. Further, combinational studies were performed in both the cell lines to evaluate the interaction of drugs with kaempferol. The combination index (CI) method was used to assess the synergism of kaempferol with doxorubicin or cisplatin. Finally, morphological alterations associated with apoptosis were examined under fluorescent microscope.

Results: All compounds showed dose-dependent growth inhibition in both HCT-15 and MDA MB 231 cells. The phytochemical kaempferol showed fifty percent inhibitory concentrations (IC50) at 120±3.2 µg/ml and 64±1.2 µg/ml on HCT-15 and MDA MB 231 respectively. IC50 concentrations of doxorubicin and cisplatin on both the cell lines were achieved at 49.6±0.5 µg/ml, 25.4±2.9 µg/ml and 44±1.8 µg/ml, 40.6±0.8 µg/ml respectively. Further, in vitro therapeutic effect (IC50) of doxorubicin and cisplatin in terms of cell growth inhibition on HCT-15 cells were achieved at their one-fifth (10±0.83 µg/ml) and half (10±1.34 µg/ml) concentrations respectively when they were combined with 30 µg/ml of kaempferol individually. Simultaneously, on MDA-MB 231 cell line, the IC50 concentrations were reduced to 18±1.22 µg/ml and 15±1.87 µg/ml respectively in combination with 32 µg/ml of kaempferol. The combinational index studies revealed the synergistic association of kaempferol with doxorubicin and cisplatin individually in each cell line. The fluorescence imaging studies strongly supported the synergistic association between kaempferol and doxorubicin or cisplatin by confirming significant apoptotic cell death in both the cell lines which was ~3 fold higher than each agent alone.

Conclusion: The study reveals the prominent synergism between the phytochemical, kaempferol and chemotherapeutic drugs doxorubicin or cisplatin which helps in elevating the therapeutic efficacy of drugs.

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References

Bharathi Raja Subramaniya, Gayathri Srinivasan, Sakeena Sadullah Mohammed Sadullah, Nimitha Davis, Lakshmi Baddi Reddi Subhadara, Devaraj Halagowder, et al. Apoptosis-inducing effect of plumbagin on colonic cancer cells depends on expression of COX-2. PLoS One 2011;6:e18695.

Catherine C, Neto. Cranberry and Its phytochemicals: a review of in vitro anticancer studies. J Nutr 2007;137:186S–193S.

Surh, Young-Joon. Cancer chemoprevention with dietary phytochemicals. Nat Rev Cancer 2003;3:768-80.

Wang D, Lippard SJ. Cellular processing of platinum anticancer drugs. Nat Rev Drug Discovery 2005;4:307-20.

Eun Jeong Choi, Woong Shick Ahn. Kaempferol induced the apoptosis via cell cycle arrest in human breast cancer MDA-MB-453 cells. Nutr Res Pract 2008;2:322-5.

S Aisling Aheme, Joseph P Kerry, Nora MO Brein. Effects of plant extract on antioxidant-induced stress in caco-2 cells. Br J Nutr 2007;97:321-8.

Liu RH. Potential synergy of phytochemicals in cancer prevention: mechanism of action. J Nutr 2004;134:3479-85.

Ranjit, Pusapati Madan, MR Krishna, P Silpa, V Nagalakshmi, M Anjali, et al. In vitro cytotoxic activities of Calotropis procera latex and flower extracts against MCF-7 and HeLa cell line cultures. Int J Pharm Pharm Sci 2012;4:66-70.

Kanadaswami, Chithan, Lung-Ta Lee, Ping-Ping H Lee, Jiuan-Jiuan Hwang, Ferng-Chun Ke, et al. The antitumor activities of flavonoids. In Vivo 2005;19:895-909.

Shu L, Cheung KL, Khor TO, Chen C, Kong AN. Phytochemicals: cancer chemoprevention and suppression of tumour onset and metastasis. Cancer Metastasis Rev 2010;29:483-502.

Margaret Leigh ackland, Simone van de waarsenburg, Rod jones. The synergistic antiproliferative action of the flavonols quercetin and kaempferol in human cancer cell lines. In Vivo 2005;19:69-76.

Gupta S. Molecular signalling in death receptor and mitochondrial pathways of apoptosis. Int J Oncol 2003;22:15-20.

Graciela Cristina dos Santos, Leonardo Meneghin Mendonça, Gilmara Ausech Antonucci, Antonio Cardozo dos Santos, Lusânia Maria Greggi Antunes and Maria, de Lourdes Pires Bianch. Protective effect of bixin on cisplatin-induced genotoxicity in PC12 cells. Food Chem Toxicol 2012;50:335-40.

Murakami A, Ohigashi H, Koshimizu K. Antitumor promotion with food phytochemicals: a strategy for cancer chemo-prevention. Biosci Biotechnol Biochem 1996;60:1-8.

Russo GL. The ins and outs of dietary phytochemicals in cancer chemoprevention. Biochem Pharmacol 2007;74:533-44.

Liu RH. Health benefits of fruit and vegetables are from additive and synergistic combinations of phytochemicals. Am J Clin Nutr 2003;78:517-20.

Balakrishnan, Shyam Kumar, K Ishwar Bhat. Apoptosis and flow cytometric studies of Bauhinia variegata bark extract. Asian J Pharm Clin Res 2014;7:45-7.

Rabik AC, Dolan MK. Molecular mechanisms of resistance and toxicity associated with platinating agents. Cancer Treatment Rev 2007;33:9-23.

Regine Lüpertz, Wim Wätjen, Regine Kahl, Yvonni Chovolou. Dose and time-dependent effects of doxorubicin on cytotoxicity, cell cycle and apoptotic cell death in human colon cancer cells. Toxicology 2010;271:115–21.

Wang G, Zhang J, Liu L, Sharma S, Dong Q. Quercetin potentiates doxorubicin-mediated antitumor effects against liver cancer through p53/Bcl-xl. PLoS One 2012;7:e51764.

Published

01-02-2017

How to Cite

Kalyani, C., M. L. Narasu, and Y. P. Devi. “SYNERGISTIC GROWTH INHIBITORY EFFECT OF FLAVONOL–KAEMPFEROL AND CONVENTIONAL CHEMOTHERAPEUTIC DRUGS ON CANCER CELLS”. International Journal of Pharmacy and Pharmaceutical Sciences, vol. 9, no. 2, Feb. 2017, pp. 123-7, doi:10.22159/ijpps.2017v9i2.16021.

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