GRIM-19:调节抗肿瘤和先天免疫反应的双刃剑

Shreeram C Nallar, S. Kalakonda, P. Sun, D. Kalvakolanu
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引用次数: 5

摘要

与类视黄素-干扰素-β诱导死亡(GRIM)相关的基因19最初被确定为干扰素-β-视黄酸诱导细胞死亡所必需的关键调控蛋白。GRIM-19过表达可激活细胞死亡,抑制或失活可促进细胞生长。GRIM-19靶向多种蛋白/途径,发挥生长控制和细胞死亡。然而,正常的细胞过程也需要GRIM-19。此外,病毒为了生存“劫持”了GRIM-19。细胞内细菌感染和细菌产物可诱导GRIM-19的表达。在这篇综述中,我们将讨论GRIM-19在生长控制和先天免疫应答中的研究现状。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
GRIM-19: A Double-edged Sword that Regulates Anti-Tumor and Innate Immune Responses
Gene associated with retinoid-interferon-β-induced mortality (GRIM)—19, was originally identified as a critical regulatory protein necessary for Interferon-β-Retinoic acid-induced cell death. Overexpression of GRIM-19 activates cell death and its suppression or inactivation promotes cell growth. GRIM-19 targets multiple proteins/pathways for exerting growth control and cell death. However, GRIM-19 is also required for normal cellular processes. In addition, viruses ‘hijack’ GRIM-19 for their survival. Intracellular bacterial infections and bacterial products have been reported to induce the expression of GRIM-19. In this review, we will discuss the current status of GRIM-19 in growth control and innate immune response.
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