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STING 信号在癌细胞中的作用:重要还是不重要?

STING Signaling in Cancer Cells: Important or Not?

机构信息

Laboratory of Experimental Medicine, Centre of New Technologies, University of Warsaw, Banacha 2c, 02-097, Warsaw, Poland.

Department of Immunology, Center of Biostructure Research, Medical University of Warsaw, Warsaw, Poland.

出版信息

Arch Immunol Ther Exp (Warsz). 2018 Apr;66(2):125-132. doi: 10.1007/s00005-017-0481-7. Epub 2017 Jul 26.

DOI:10.1007/s00005-017-0481-7
PMID:28748479
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5851689/
Abstract

Stimulator of interferon genes (STING) is an adaptor protein that plays an important role in the activation of type I interferons in response to cytosolic nucleic acid ligands. Recent evidence indicates involvement of the STING pathway in the induction of antitumor immune response. Therefore, STING agonists are now being extensively developed as a new class of cancer therapeutics. However, little is known about the consequences of activated STING-mediated signaling in cancer cells on the efficacy of the antitumor treatment. It has been shown that activation of the STING-dependent pathway in cancer cells can result in tumor infiltration with immune cells and modulation of the anticancer immune response. Understanding the function of STING pathway in cancer cells might provide important insights into the development of effective therapeutic strategies. This review focuses on the role of STING pathway in cancer cells, the largely unknown topic that has recently emerged to be important in the context of STING-mediated antitumor responses.

摘要

干扰素基因刺激物 (STING) 是一种衔接蛋白,在细胞溶质核酸配体对 I 型干扰素的激活中发挥重要作用。最近的证据表明,STING 途径参与了抗肿瘤免疫反应的诱导。因此,STING 激动剂目前正在被广泛开发为一类新的癌症治疗药物。然而,对于激活的 STING 介导的信号在癌细胞中对抗肿瘤治疗效果的影响知之甚少。已经表明,癌细胞中 STING 依赖性途径的激活可导致肿瘤浸润免疫细胞和抗肿瘤免疫反应的调节。了解 STING 途径在癌细胞中的功能可能为开发有效的治疗策略提供重要的见解。本综述重点介绍 STING 途径在癌细胞中的作用,这是一个最近出现的重要课题,在 STING 介导的抗肿瘤反应中具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebc0/5851689/22c6504a6849/5_2017_481_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebc0/5851689/93326025a4cb/5_2017_481_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebc0/5851689/22c6504a6849/5_2017_481_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebc0/5851689/93326025a4cb/5_2017_481_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebc0/5851689/22c6504a6849/5_2017_481_Fig2_HTML.jpg

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Semin Oncol. 2016 Dec;43(6):638-646. doi: 10.1053/j.seminoncol.2016.10.005. Epub 2016 Oct 27.
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DNA-Sensing and Nuclease Gene Expressions as Markers for Colorectal Cancer Progression.DNA 传感与核酸酶基因表达作为结直肠癌进展的标志物
Oncology. 2017;92(2):115-124. doi: 10.1159/000452281. Epub 2016 Dec 17.
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Intracellular STING inactivation sensitizes breast cancer cells to genotoxic agents.
结直肠癌中癌相关成纤维细胞对肿瘤细胞中cGAS/STING表达的下调作用
Sci Rep. 2025 Jun 2;15(1):19234. doi: 10.1038/s41598-025-03924-6.
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Progress Update on STING Agonists as Vaccine Adjuvants.作为疫苗佐剂的STING激动剂的进展更新
Vaccines (Basel). 2025 Mar 31;13(4):371. doi: 10.3390/vaccines13040371.
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Dendritic cell maturation in cancer.癌症中的树突状细胞成熟
Nat Rev Cancer. 2025 Apr;25(4):225-248. doi: 10.1038/s41568-024-00787-3. Epub 2025 Feb 7.
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High levels of tumor cell-intrinsic STING signaling are associated with increased infiltration of CD8 T cells in dMMR/MSI-H gastric cancer.高水平的肿瘤细胞固有 STING 信号与 dMMR/MSI-H 胃癌中 CD8 T 细胞浸润增加有关。
Sci Rep. 2024 Sep 6;14(1):20859. doi: 10.1038/s41598-024-71974-3.
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Loss of the DNA repair protein, polynucleotide kinase/phosphatase, activates the type 1 interferon response independent of ionizing radiation.DNA 修复蛋白多核苷酸激酶/磷酸酶缺失会激活 I 型干扰素反应,而与电离辐射无关。
Nucleic Acids Res. 2024 Sep 9;52(16):9630-9653. doi: 10.1093/nar/gkae654.
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Activation of STING requires palmitoylation at the Golgi.STING 的激活需要在高尔基体上进行棕榈酰化。
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