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细胞周期蛋白依赖性激酶抑制剂、罗斯考维汀和嘌呤醇可诱导人宫颈癌HeLa细胞中与未折叠蛋白反应相关的细胞凋亡和自噬。

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

作者信息

Ozfiliz-Kilbas Pelin, Sarikaya Bahar, Obakan-Yerlikaya Pinar, Coker-Gurkan Ajda, Arisan Elif Damla, Temizci Benan, Palavan-Unsal Narcin

机构信息

Department of Molecular Biology and Genetics, Istanbul Kultur University, Atakoy Campus, 34156, Istanbul, Turkey.

出版信息

Mol Biol Rep. 2018 Oct;45(5):815-828. doi: 10.1007/s11033-018-4222-8. Epub 2018 Jul 5.

Abstract

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.

摘要

罗可辛(Roscovitine,Rosc)和嘌呤醇(Purvalanol,Pur)通过靶向细胞周期蛋白依赖性激酶(CDKs)的ATP结合口袋来竞争性抑制这些激酶。已证明这两种药物均能有效降低细胞活力,并失调促凋亡和抗凋亡Bcl-2家族成员的比例,最终导致体外不同癌细胞系中的细胞凋亡死亡。众所周知,Bcl-2家族成员在调节其他细胞过程(如内质网(ER)应激)中具有不同作用。内质网应激的诱导已被证明在通过自噬或凋亡进行的细胞死亡/存活决定中起关键作用。在本研究中,我们的目的是以时间依赖性方式研究CDK抑制剂在HeLa宫颈癌细胞中与不同细胞死亡类型相关的内质网应激机制上的分子靶点。我们的结果表明,Rosc和Pur以时间依赖性方式降低细胞活力、细胞生长和集落形成,诱导内质网应激介导的自噬或凋亡。因此,我们得出结论,HeLa宫颈癌细胞暴露于CDK抑制剂会诱导未折叠蛋白反应和内质网应激,从而导致自噬和凋亡过程。

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