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cGAS-STING信号通路与肝脏疾病:从基础研究到临床实践

cGAS-STING Signaling Pathway and Liver Disease: From Basic Research to Clinical Practice.

作者信息

Chen Bangjie, Rao Xianyue, Wang Xinyi, Luo Zhipan, Wang Jianpeng, Sheng Shuyan, Liu Yuchen, Zhang Ning, Jin Shiyu, Chen Haosong, Sun Chenyu, Xu Tao, Du Yingying

机构信息

The First Affiliated Hospital of Anhui Medical University, Hefei, China.

First Clinical Medical College, Anhui Medical University, Heifei, China.

出版信息

Front Pharmacol. 2021 Aug 18;12:719644. doi: 10.3389/fphar.2021.719644. eCollection 2021.

DOI:10.3389/fphar.2021.719644
PMID:34483930
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8416453/
Abstract

The cGAS-STING signaling pathway is an autoimmune inflammatory pathway that can trigger the expression of a series of inflammatory factors represented by type 1 interferon. Recent studies have found that the cGAS-STING signaling pathway played a significant role in liver physiology and was closely related to the progress of liver diseases. For example, activating the cGAS-STING signaling pathway could significantly inhibit hepatitis B virus (HBV) replication in vivo. Moreover, the cGAS-STING signaling pathway was also closely associated with tumor immunity in hepatocellular carcinoma (HCC). This review summarized the role of the cGAS-STING signaling pathway in several common liver diseases, especially the current application of the cGAS-STING signaling pathway in liver disease treatment, and prospected its future research, which provided a new idea for understanding and treating liver diseases.

摘要

cGAS-STING信号通路是一条自身免疫炎症通路,可触发以1型干扰素为代表的一系列炎症因子的表达。最近的研究发现,cGAS-STING信号通路在肝脏生理过程中发挥着重要作用,且与肝脏疾病的进展密切相关。例如,激活cGAS-STING信号通路可在体内显著抑制乙型肝炎病毒(HBV)复制。此外,cGAS-STING信号通路还与肝细胞癌(HCC)的肿瘤免疫密切相关。本综述总结了cGAS-STING信号通路在几种常见肝脏疾病中的作用,尤其是cGAS-STING信号通路在肝脏疾病治疗中的当前应用,并对其未来研究进行了展望,为理解和治疗肝脏疾病提供了新思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3e9/8416453/2f72959cd766/fphar-12-719644-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3e9/8416453/4f025dae9294/fphar-12-719644-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3e9/8416453/12856f417db6/fphar-12-719644-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3e9/8416453/2f72959cd766/fphar-12-719644-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3e9/8416453/4f025dae9294/fphar-12-719644-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3e9/8416453/12856f417db6/fphar-12-719644-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3e9/8416453/2f72959cd766/fphar-12-719644-g003.jpg

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J Control Release. 2021 Mar 10;331:480-490. doi: 10.1016/j.jconrel.2021.01.036. Epub 2021 Feb 3.
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Mutant p53 suppresses innate immune signaling to promote tumorigenesis.突变型 p53 抑制先天免疫信号转导以促进肿瘤发生。
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Phosphorylation and chromatin tethering prevent cGAS activation during mitosis.
沉默破坏:乙型肝炎病毒-miR-3如何通过抑制cGAS-STING解除先天免疫
World J Hepatol. 2025 Jun 27;17(6):106493. doi: 10.4254/wjh.v17.i6.106493.
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Optimizing delivery in a multivalent subunit influenza vaccine using mixed polymeric microparticle degradation rates.利用混合聚合物微粒降解速率优化多价亚单位流感疫苗的递送
J Control Release. 2025 Aug 10;384:113936. doi: 10.1016/j.jconrel.2025.113936. Epub 2025 Jun 6.
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Targeting cGAS-STING: modulating the immune landscape of hepatic diseases.靶向环鸟苷酸-腺苷酸合成酶-干扰素基因刺激蛋白:调节肝脏疾病的免疫格局
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Oncol Rep. 2025 Jan;53(1). doi: 10.3892/or.2024.8848. Epub 2024 Nov 29.
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