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内质网应激与自噬相互作用诱导突变型 p53H273 降解。

Interplay between Endoplasmic Reticulum (ER) Stress and Autophagy Induces Mutant p53H273 Degradation.

机构信息

Department of Research and Advanced Technologies, IRCCS Regina Elena National Cancer Institute, 00144 Rome, Italy.

University "G. D'Annunzio", School of Medicine, 66100 Chieti, Italy.

出版信息

Biomolecules. 2020 Mar 3;10(3):392. doi: 10.3390/biom10030392.

Abstract

The unfolded protein response (UPR) is an adaptive response to intrinsic and external stressors, and it is mainly activated by the accumulation of misfolded proteins at the endoplasmic reticulum (ER) lumen producing ER stress. The UPR signaling network is interconnected with autophagy, the proteolytic machinery specifically devoted to clearing misfolded proteins in order to survive bioenergetic stress and/or induce cell death. Oncosuppressor TP53 may undergo inactivation following missense mutations within the DNA-binding domain (DBD), and mutant p53 (mutp53) proteins may acquire a misfolded conformation, often due to the loss of the DBD-bound zinc ion, leading to accumulation of hyperstable mutp53 proteins that correlates with more aggressive tumors, resistance to therapies, and poorer outcomes. We previously showed that zinc supplementation induces mutp53 protein degradation by autophagy. Here, we show that mutp53 (i.e., Arg273) degradation following zinc supplementation is correlated with activation of ER stress and of the IRE1α/XBPI arm of the UPR. ER stress inhibition with chemical chaperone 4-phenyl butyrate (PBA) impaired mutp53 downregulation, which is similar to IRE1α/XBPI specific inhibition, reducing cancer cell death. Knockdown of mutp53 failed to induce UPR/autophagy activation indicating that the effect of zinc on mutp53 folding was likely the key event occurring in ER stress activation. Recently discovered small molecules targeting components of the UPR show promise as a novel anticancer therapeutic intervention. However, our findings showing UPR activation during mutp53 degradation indicate that caution is necessary in the design of therapies that inhibit UPR components.

摘要

未折叠蛋白反应(UPR)是一种对内源性和外源性应激的适应性反应,主要由内质网(ER)腔中错误折叠蛋白的积累引起 ER 应激而激活。UPR 信号网络与自噬相互连接,自噬是一种专门用于清除错误折叠蛋白的蛋白水解机制,以在生物能量应激下存活和/或诱导细胞死亡。肿瘤抑制因子 TP53 可能会在 DNA 结合域(DBD)内的错义突变后失活,突变型 p53(mutp53)蛋白可能获得错误折叠的构象,通常是由于 DBD 结合的锌离子丢失,导致超稳定 mutp53 蛋白的积累,这与更具侵袭性的肿瘤、对治疗的耐药性和较差的预后相关。我们之前表明,锌补充通过自噬诱导 mutp53 蛋白降解。在这里,我们表明锌补充后 mutp53(即 Arg273)的降解与 ER 应激和 UPR 的 IRE1α/XBPI 分支的激活相关。用化学伴侣 4-苯基丁酸(PBA)抑制 ER 应激会损害 mutp53 的下调,这类似于 IRE1α/XBPI 的特异性抑制,从而减少癌细胞死亡。mutp53 的敲低未能诱导 UPR/自噬的激活,表明锌对 mutp53 折叠的影响可能是 ER 应激激活中发生的关键事件。最近发现的靶向 UPR 成分的小分子作为一种新的抗癌治疗干预手段显示出前景。然而,我们的研究结果表明,在 mutp53 降解过程中激活了 UPR,这表明在设计抑制 UPR 成分的治疗方法时需要谨慎。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc70/7175121/768696d5f7b9/biomolecules-10-00392-g001.jpg

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