Sood Ashita
Centre for Computational Biology and Bioinformatics, Central University of Himachal Pradesh, Dharamsala, India.
Immunol Res. 2025 Jun 9;73(1):91. doi: 10.1007/s12026-025-09648-z.
The cGAS-STING pathway is a critical signaling mechanism in the innate immune system for sensing cytosolic DNA and subsequently facilitating antiviral responses. Cyclic GMP-AMP synthase (cGAS) recognizes both foreign and self-DNA in the cytosol, resulting in the formation of 2'3'-cyclic GMP-AMP. STING is activated by the cyclic dinucleotide and drives the production of type I interferons as well as pro-inflammatory cytokines. Generating an inflammatory response through the cGAS-STING pathway is critical for antiviral defense, and this cascade also has been involved in the regulation of autophagy, cellular senescence, and other diseases. Defects in this pathway can result in autoimmunity, chronic inflammation, or increased cancer susceptibility. The molecular mechanisms underlying this pathway, its regulatory factors, and how it may contribute to diseases such as systemic lupus erythematosus (SLE), rheumatoid arthritis, and certain cancers were reviewed. This review further covers the therapeutic approaches to this system, such as agonists for cancer treatment and antagonists for autoimmune diseases.
cGAS-STING通路是天然免疫系统中一种关键的信号传导机制,用于感知胞质DNA并随后促进抗病毒反应。环状GMP-AMP合酶(cGAS)识别胞质中的外源和自身DNA,导致2'3'-环状GMP-AMP的形成。STING被环状二核苷酸激活,并驱动I型干扰素以及促炎细胞因子的产生。通过cGAS-STING通路产生炎症反应对抗病毒防御至关重要,并且该级联反应还参与了自噬、细胞衰老和其他疾病的调节。该通路的缺陷可导致自身免疫、慢性炎症或癌症易感性增加。本文综述了该通路的分子机制、其调节因子以及它如何导致系统性红斑狼疮(SLE)、类风湿性关节炎和某些癌症等疾病。本综述还进一步涵盖了针对该系统的治疗方法,例如用于癌症治疗的激动剂和用于自身免疫性疾病的拮抗剂。