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内质网应激信号与肝癌的发病机制。

Endoplasmic Reticulum Stress Signaling and the Pathogenesis of Hepatocarcinoma.

机构信息

Department of Pathology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA.

出版信息

Int J Mol Sci. 2021 Feb 11;22(4):1799. doi: 10.3390/ijms22041799.

Abstract

Hepatocellular carcinoma (HCC), also known as hepatoma, is a primary malignancy of the liver and the third leading cause of cancer mortality globally. Although much attention has focused on HCC, its pathogenesis remains largely obscure. The endoplasmic reticulum (ER) is a cellular organelle important for regulating protein synthesis, folding, modification and trafficking, and lipid metabolism. ER stress occurs when ER homeostasis is disturbed by numerous environmental, physiological, and pathological challenges. In response to ER stress due to misfolded/unfolded protein accumulation, unfolded protein response (UPR) is activated to maintain ER function for cell survival or, in cases of excessively severe ER stress, initiation of apoptosis. The liver is especially susceptible to ER stress given its protein synthesis and detoxification functions. Experimental data suggest that ER stress and unfolded protein response are involved in HCC development, aggressiveness and response to treatment. Herein, we highlight recent findings and provide an overview of the evidence linking ER stress to the pathogenesis of HCC.

摘要

肝细胞癌(HCC),又称肝癌,是肝脏的原发性恶性肿瘤,也是全球癌症死亡的第三大主要原因。尽管人们对 HCC 给予了高度关注,但它的发病机制在很大程度上仍不清楚。内质网(ER)是一种对调节蛋白质合成、折叠、修饰和运输以及脂质代谢非常重要的细胞细胞器。当内质网的内环境平衡受到许多环境、生理和病理挑战的干扰时,就会发生内质网应激。当由于错误折叠/未折叠蛋白积累而导致内质网应激时,未折叠蛋白反应(UPR)被激活以维持内质网功能以促进细胞存活,或者在内质网应激过于严重的情况下,启动细胞凋亡。由于肝脏具有蛋白质合成和解毒功能,因此尤其容易受到内质网应激的影响。实验数据表明,内质网应激和未折叠蛋白反应参与了 HCC 的发生、侵袭性和对治疗的反应。在此,我们强调了最近的发现,并概述了将内质网应激与 HCC 发病机制联系起来的证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f820/7918477/81126badedd3/ijms-22-01799-g001.jpg

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