EIF2α phosphorylation: a hallmark of both autophagy and immunogenic cell death.

Molecular & cellular oncology Pub Date : 2020-06-19 eCollection Date: 2020-01-01 DOI:10.1080/23723556.2020.1776570
Juliette Humeau, Lucillia Bezu, Oliver Kepp, Guido Kroemer
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引用次数: 14

Abstract

Different intrinsic and extrinsic stress pathways including endoplasmic reticulum (ER) stress converge on the phosphorylation of eukaryotic translation initiation factor 2A (EIF2A, best known as eIF2α), which characterizes the so-called "integrated stress response". This phosphorylation event is important for the induction of autophagy in response to multiple distinct stressors, as well as for the exposure of calreticulin (CALR) as an "eat me" signal on the surface of the plasma membrane of stressed cells. Both autophagy and CALR exposure are required for immunogenic cell death, a modality of cellular demise that ignites anticancer and antiviral immune responses. In several different cancer types, eIF2α phosphorylation indicates favorable prognosis, correlating with an enhanced antitumor immune response.

EIF2α磷酸化:自噬和免疫原性细胞死亡的标志。
包括内质网(ER)应激在内的不同内源性和外源性应激途径汇聚于真核生物翻译起始因子2A (EIF2A,最广为人知的是eIF2α)的磷酸化,这是所谓的“综合应激反应”的特征。这种磷酸化事件对于诱导多种不同应激源的自噬反应以及钙网蛋白(CALR)暴露于应激细胞的质膜表面作为“吃我”信号是重要的。免疫原性细胞死亡需要自噬和CALR暴露,这是细胞死亡的一种方式,可引发抗癌和抗病毒免疫反应。在几种不同的癌症类型中,eIF2α磷酸化预示着良好的预后,与增强的抗肿瘤免疫反应相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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