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首页> 外文期刊>European review for medical and pharmacological sciences. >Withaferin-A induces apoptosis in osteosarcoma U2OS cell line via generation of ROS and disruption of mitochondrial membrane potential
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Withaferin-A induces apoptosis in osteosarcoma U2OS cell line via generation of ROS and disruption of mitochondrial membrane potential

机译:Withaferin-A通过产生ROS和破坏线粒体膜电位来诱导骨肉瘤U2OS细胞凋亡

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OBJECTIVE: Withaferin-A (WF-A) is a well-known dietary compound isolated from Withania somnifera. It has marked pharmacological potential and has been shown to exhibit antiproliferative activity against several types of cancerous cells. Currently, the main focus of anti-cancer therapeutic development is to identify apoptosis-inducing drug-like molecules. Osteosarcoma is a rare type of bone cancer affecting humans. The objective of the present study was therefore to evaluate the antitumor potential of WF-A against several osteosarcoma cell lines. MATERIALS AND METHODS: MTT assay was used to evaluate WF-A against osteosarcoma cell lines and to calculate the IC50. DAPI staining was used to confirm the apoptosis-inducing potential of WF-A. Mitochondrial membrane potential, reactive oxygen species (ROS) assay, and Western blotting were used to confirm the basis of apoptosis. RESULTS: The results of the present study revealed that WF-A exhibited strong antiproliferative activity against all the cells lines, with IC50 ranging from 0.32 to 7.6 μM. The lowest IC50 (0.32 μM) was observed against U2OS cell line and, therefore, it was selected for further analysis. DAPI staining indicated that WF-A exhibited antiproliferative activity via induction of apoptosis. Moreover, WF-A induced a ROS-mediated reduction in mitochondrial membrane potential in a dose-dependent manner and activation of caspase-3 in osteosarcoma cells. CONCLUSIONS: We suggest that WF-A may prove a potent therapeutic agent for inducing apoptosis in osteosarcoma cell lines via generation of ROS and disruption of mitochondrial membrane potential.
机译:目的:Withaferin-A(WF-A)是从Withania somnifera中分离出来的一种众所周知的饮食化合物。它具有显着的药理学潜力,并已显示出对几种类型的癌细胞的抗增殖活性。当前,抗癌治疗发展的主要焦点是鉴定诱导凋亡的药物样分子。骨肉瘤是一种罕见的影响人类的骨癌。因此,本研究的目的是评估WF-A对几种骨肉瘤细胞系的抗肿瘤潜力。材料与方法:采用MTT法评价WF-A对骨肉瘤细胞的杀伤力,并计算IC50。 DAPI染色用于确认WF-A的凋亡诱导潜力。线粒体膜电位,活性氧(ROS)测定法和蛋白质印迹法被用来确定细胞凋亡的基础。结果:本研究结果显示WF-A对所有细胞系均表现出较强的抗增殖活性,IC50为0.32至7.6μM。观察到针对U2OS细胞系的最低IC50(0.32μM),因此选择进行进一步分析。 DAPI染色表明WF-A通过诱导细胞凋亡显示出抗增殖活性。而且,WF-A以剂量依赖的方式诱导了ROS介导的线粒体膜电位的降低和骨肉瘤细胞中caspase-3的活化。结论:我们认为WF-A可能是通过产生ROS和破坏线粒体膜电位而诱导骨肉瘤细胞凋亡的有效治疗剂。

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