Anticancer Activity of Cobra Venom Polypeptide, Cytotoxin-II, against Human Breast Adenocarcinoma Cell Line (MCF-7) via the Induction of Apoptosis.
10.4048/jbc.2014.17.4.314
- Author:
Karim EBRAHIM
1
;
Farshad H SHIRAZI
;
Hosein VATANPOUR
;
Abas ZARE
;
Farzad KOBARFARD
;
Hadi RABIEI
Author Information
1. Department of Toxicology, Shahid Beheshti University of Medical Sciences School of Pharmacy, Tehran, Iran. k.najafabady@sbmu.ac.ir
- Publication Type:Original Article
- Keywords:
Apoptosis;
Breast neoplasms;
Cytotoxins;
Snakes;
Venoms
- MeSH:
Adenocarcinoma*;
Antineoplastic Agents;
Apoptosis*;
Biological Products;
Breast Neoplasms;
Breast*;
Caspase 9;
Cell Cycle Checkpoints;
Cell Death;
Cell Line*;
Cisplatin;
Cobra Venoms*;
Cytotoxins;
Diagnosis;
Elapidae;
Female;
Humans;
MCF-7 Cells;
Membrane Potential, Mitochondrial;
Peptides;
Reactive Oxygen Species;
Snakes;
Venoms
- From:Journal of Breast Cancer
2014;17(4):314-322
- CountryRepublic of Korea
- Language:English
-
Abstract:
PURPOSE: Breast cancer is a significant health problem worldwide, accounting for a quarter of all cancer diagnoses in women. Current strategies for breast cancer treatment are not fully effective, and there is substantial interest in the identification of novel anticancer agents especially from natural products including toxins. Cytotoxins are polypeptides found in the venom of cobras and have various physiological effects. In the present study, the anticancer potential of cytotoxin-II against the human breast adenocarcinoma cell line (MCF-7) was investigated. METHODS: The cytotoxic effects of cytotoxin-II were determined by morphological analysis and 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay. The mode and mechanism of cell death were investigated via acridine orange/ethidium bromide (AO/EtBr) double staining, flow cytometric analysis of cell death, detection of mitochondrial membrane potential, measurement of intracellular reactive oxygen species (ROS), annexin V/propidium iodide staining, and caspase-9 activity assays. RESULTS: The half maximal inhibitory concentration (IC50) of cytotoxin-II in MCF-7 cells was 4.18+/-1.23 microg/mL, while the value for cisplatin was approximately 28.02+/-1.87 microg/mL. Morphological analysis and AO/EtBr double staining showed typical manifestations of apoptotic cell death (in doses lower than 8 microg/mL). Dose- and time-dependent ROS generation, loss of mitochondrial membrane potential, caspase-9 activation, and cell cycle arrest were observed in their respective tests. CONCLUSION: In conclusion, cytotoxin-II has potent anticancer effects in the MCF-7 cell line, which are induced via the intrinsic pathways of apoptosis. Based on these findings, cytotoxin-II is a suitable choice for breast cancer treatment.
