赫拉
细胞凋亡
碘化丙啶
活力测定
MTT法
癌细胞
生物
线粒体
程序性细胞死亡
化学
癌症研究
细胞
分子生物学
细胞生物学
癌症
生物化学
遗传学
作者
Juanli Wang,Hong Wu,Gui‐Ting Song,Donglin Yang,Jiuhong Huang,Xiaofang Yao,Qin Hongxia,Zhong‐Zhu Chen,Zhigang Xu,Chuan Xu
摘要
Background . Cancer remains a major clinical challenge because of the lack of effective drug for its treatment. To find out novel cancer chemotherapeutic molecules, we explored the anticancer effect of novel imidazopyridine compound 9i and also investigated the underlying molecular mechanism. Methods . Human cervical cancer cell (HeLa) viability was measured by an MTT assay after treatment with compound 9i . Clonogenicity of HeLa cells was investigated by an in vitro colony formation assay. Cell death was visualized by propidium iodide (PI) staining. Fluorescence‐activated cell sorting (FACS) was used to determine apoptosis and mitochondrial membrane potential in HeLa cells. The expression level of apoptosis‐related proteins was also determined by western blot. Results . Compound 9i suppressed HeLa cell viability in a time‐ and dose‐dependent manner. Compound 9i induced mitochondrial outer membrane permeabilization (MOMP), activated caspase cascade, and finally resulted in apoptosis. Conclusion . Compound 9i induces mitochondrial pathway‐mediated apoptosis in human cervical cancer cells, suggesting that 9i could be a potential lead compound to be developed as a cancer therapeutic molecule.
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