展开的蛋白质反应是肿瘤的福音,也是免疫系统的福音。

Lydia N Raines, Stanley Ching-Cheng Huang
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摘要

蛋白质的正确折叠对适当的细胞功能至关重要,并且在内质网(ER)内受到严格调节。环境挑战和细胞条件破坏内质网稳态并诱导内质网应激,从而对蛋白质折叠产生不利影响并激活未折叠蛋白质反应(UPR)。现在人们认识到,癌症细胞可以通过激活UPR来克服肿瘤微环境中的生存挑战。此外,还发现UPR通过在肿瘤浸润的先天免疫细胞和适应性免疫细胞中诱导免疫抑制活性,对免疫细胞产生有害影响。这表明这些信号轴可能是重要的治疗靶点,从而产生根除肿瘤细胞的多方面方法。在这篇微观综述中,我们讨论了UPR在驱动肿瘤进展和调节免疫系统靶向癌症细胞能力方面的作用。此外,我们强调了一些可能指导未来普遍定期审议研究的关键问题。
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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How the Unfolded Protein Response Is a Boon for Tumors and a Bane for the Immune System.

The correct folding of proteins is essential for appropriate cell function and is tightly regulated within the endoplasmic reticulum (ER). Environmental challenges and cellular conditions disrupt ER homeostasis and induce ER stress, which adversely affect protein folding and activate the unfolded protein response (UPR). It is now becoming recognized that cancer cells can overcome survival challenges posed within the tumor microenvironment by activating the UPR. Furthermore, the UPR has also been found to impose detrimental effects on immune cells by inducing immunoinhibitory activity in both tumor-infiltrating innate and adaptive immune cells. This suggests that these signaling axes may be important therapeutic targets, resulting in multifaceted approaches to eradicating tumor cells. In this mini-review, we discuss the role of the UPR in driving tumor progression and modulating the immune system's ability to target cancer cells. Additionally, we highlight some of the key unanswered questions that may steer future UPR research.

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