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Cyclin-dependent kinase inhibitors, roscovitine and purvalanol, induce apoptosis and autophagy related to unfolded protein response in HeLa cervical cancer cells

机译:细胞周期蛋白依赖性激酶抑制剂,Roscovitine和Purvalanol,诱导凋亡和自噬与HeLa宫颈癌细胞中展开的蛋白质反应相关

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摘要

Roscovitine (Rosc) and purvalanol (Pur) are competitive inhibitors of cyclin-dependent kinases (CDKs) by targeting their ATP-binding pockets. Both drugs are shown to be effective to decrease cell viability and dysregulate the ratio of pro- and anti-apoptotic Bcl-2 family members, which finally led to apoptotic cell death in different cancer cell lines in vitro. It was well established that Bcl-2 family members have distinct roles in the regulation of other cellular processes such as endoplasmic reticulum (ER) stress. The induction of ER stress has been shown to play critical role in cell death/survival decision via autophagy or apoptosis. In this study, our aim was to investigate the molecular targets of CDK inhibitors on ER stress mechanism related to distinct cell death types in time-dependent manner in HeLa cervical cancer cells. Our results showed that Rosc and Pur decreased the cell viability, cell growth and colony formation, induced ER stress-mediated autophagy or apoptosis in time-dependent manner. Thus, we conclude that exposure of cells to CDK inhibitors induces unfolded protein response and ER stress leading to autophagy and apoptosis processes in HeLa cervical cancer cells.
机译:Roscovitine(ROSC)和Purvalanol(PUR)是通过靶向其ATP绑定口袋的细胞周期蛋白依赖性激酶(CDK)的竞争性抑制剂。两种药物被证明是有效降低细胞活力并使诸如抗凋亡Bcl-2家族成员的比例,最终导致在体外不同癌细胞系中的凋亡细胞死亡。明确建立了Bcl-2家族成员在调节其他细胞过程(如内质网(ER)应激的情况下具有明显的作用。已经证明ER应激的诱导在通过自噬或细胞凋亡在细胞死亡/存活决定中起重要作用。在这项研究中,我们的目的是研究CDK抑制剂对与在HeLa宫颈癌细胞的时间依赖性的不同细胞死亡类型相关的ER应激机制上的分子靶标。我们的结果表明,ROSC和PUR降低了细胞活力,细胞生长和菌落形成,诱导了ER应激介导的自噬或细胞凋亡,以时间依赖性方式。因此,我们得出结论,细胞暴露于CDK抑制剂诱导展开的蛋白质反应和ER应激,导致HeLa宫颈癌细胞中的自噬和凋亡过程。

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