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肿瘤微环境中 cGAS-STING 信号通路的免疫调节及其临床应用
Authors Pu F, Chen F, Liu J, Zhang Z, Shao Z
Received 24 December 2020
Accepted for publication 19 February 2021
Published 1 March 2021 Volume 2021:14 Pages 1501—1516
DOI https://doi.org/10.2147/OTT.S298958
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 2
Editor who approved publication: Dr Leo Jen-Liang Su
Abstract: As a DNA receptor in the cytoplasm, cyclic GMP-AMP synthase (cGAS) contributes to the recognition of abnormal DNA in the cytoplasm and contributes to the stimulator of interferon genes (STING) signaling pathway. cGAS could mediate the expression of interferon-related genes, inflammatory-related factors, and downstream chemokines, thus initiating the immune response. The STING protein is a key effector downstream of the DNA receptor pathway. It is widely expressed across cell types such as immune cells, tumor cells, and stromal cells and plays a role in signal transduction for cytoplasmic DNA sensing and immunity. STING agonists, as novel agonists, are used in preclinical research and in the treatment of various tumors via clinical trials and have displayed attractive application prospects. Studying the cGAS-STING signaling pathway will deepen our understanding of tumor immunity and provide a basis for the research and development of antitumor drugs.
Keywords: cGAS, STING, innate immunity, tumor, immunotherapy, drug discovery