作为抗癌疗法靶点的 IRE1 的双重 RNase 活性。

IF 3.6 3区 生物学 Q3 CELL BIOLOGY
Sylwia Bartoszewska, Jakub Sławski, James F Collawn, Rafał Bartoszewski
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引用次数: 1

摘要

未折叠蛋白质反应(UPR)是一种细胞机制,在应激条件下保护细胞,在这种条件下,错误折叠的蛋白质会在内质网(ER)中积累。UPR 激活三种信号通路,这些通路的功能是缓解应激条件,促进细胞稳态和细胞存活。然而,在压力未得到缓解的情况下,UPR 激活信号通路会发生改变,通过细胞凋亡促进细胞死亡。有趣的是,癌细胞利用这一途径促进存活,即使在长期细胞应激条件下也能避免细胞凋亡。在此,我们将讨论与 UPR 相关的不同信号通路,并特别关注在 UPR 期间激活的 ER 信号通路之一--肌醇需要酶 1α(IRE1)。理由是 IRE1 通路与细胞命运的决定有关,是公认的有希望的癌症治疗靶点。在此,我们将讨论 IRE1 抑制剂及其如何成为一种有效的癌症疗法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Dual RNase activity of IRE1 as a target for anticancer therapies.

Dual RNase activity of IRE1 as a target for anticancer therapies.

The unfolded protein response (UPR) is a cellular mechanism that protects cells during stress conditions in which there is an accumulation of misfolded proteins in the endoplasmic reticulum (ER). UPR activates three signaling pathways that function to alleviate stress conditions and promote cellular homeostasis and cell survival. During unmitigated stress conditions, however, UPR activation signaling changes to promote cell death through apoptosis. Interestingly, cancer cells take advantage of this pathway to facilitate survival and avoid apoptosis even during prolonged cell stress conditions. Here, we discuss different signaling pathways associated with UPR and focus specifically on one of the ER signaling pathways activated during UPR, inositol-requiring enzyme 1α (IRE1). The rationale is that the IRE1 pathway is associated with cell fate decisions and recognized as a promising target for cancer therapeutics. Here we discuss IRE1 inhibitors and how they might prove to be an effective cancer therapeutic.

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来源期刊
CiteScore
6.40
自引率
4.90%
发文量
40
期刊介绍: The Journal of Cell Communication and Signaling provides a forum for fundamental and translational research. In particular, it publishes papers discussing intercellular and intracellular signaling pathways that are particularly important to understand how cells interact with each other and with the surrounding environment, and how cellular behavior contributes to pathological states. JCCS encourages the submission of research manuscripts, timely reviews and short commentaries discussing recent publications, key developments and controversies. Research manuscripts can be published under two different sections : In the Pathology and Translational Research Section (Section Editor Andrew Leask) , manuscripts report original research dealing with celllular aspects of normal and pathological signaling and communication, with a particular interest in translational research. In the Molecular Signaling Section (Section Editor Satoshi Kubota) manuscripts report original signaling research performed at molecular levels with a particular interest in the functions of intracellular and membrane components involved in cell signaling.
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