Ebrahim Karim, Shirazi Farshad H, Vatanpour Hosein, Zare Abas, Kobarfard Farzad, Rabiei Hadi
Department of Toxicology, Shahid Beheshti University of Medical Sciences School of Pharmacy, Tehran, Iran.
Pharmaceutical Sciences Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
J Breast Cancer. 2014 Dec;17(4):314-22. doi: 10.4048/jbc.2014.17.4.314. Epub 2014 Dec 26.
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.
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.
The half maximal inhibitory concentration (IC50) of cytotoxin-II in MCF-7 cells was 4.18±1.23 µg/mL, while the value for cisplatin was approximately 28.02±1.87 µg/mL. Morphological analysis and AO/EtBr double staining showed typical manifestations of apoptotic cell death (in doses lower than 8 µg/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.
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.
乳腺癌是全球重大的健康问题,占女性所有癌症诊断病例的四分之一。当前的乳腺癌治疗策略并不完全有效,人们对鉴定新型抗癌药物,尤其是从包括毒素在内的天然产物中鉴定新型抗癌药物有着浓厚兴趣。细胞毒素是眼镜蛇毒液中发现的多肽,具有多种生理作用。在本研究中,研究了细胞毒素-II对人乳腺腺癌细胞系(MCF-7)的抗癌潜力。
通过形态学分析和3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐试验测定细胞毒素-II的细胞毒性作用。通过吖啶橙/溴化乙锭(AO/EtBr)双重染色、细胞死亡的流式细胞术分析、线粒体膜电位检测、细胞内活性氧(ROS)测量、膜联蛋白V/碘化丙啶染色和半胱天冬酶-9活性测定来研究细胞死亡的方式和机制。
细胞毒素-II在MCF-7细胞中的半数最大抑制浓度(IC50)为4.18±1.23μg/mL,而顺铂的值约为28.02±1.87μg/mL。形态学分析和AO/EtBr双重染色显示了凋亡细胞死亡的典型表现(剂量低于8μg/mL)。在各自的试验中观察到剂量和时间依赖性的ROS生成、线粒体膜电位丧失、半胱天冬酶-9激活和细胞周期停滞。
总之,细胞毒素-II在MCF-7细胞系中具有强大的抗癌作用,这些作用是通过凋亡的内在途径诱导的。基于这些发现,细胞毒素-II是乳腺癌治疗的合适选择。