Sun Changfa, Wang Bochu, Hao Shilei
Key Laboratory of Biorheological Science and Technology, Ministry of Education, College of Bioengineering, Chongqing University, Chongqing, China.
Front Immunol. 2022 Mar 21;13:837230. doi: 10.3389/fimmu.2022.837230. eCollection 2022.
A2A receptors (A2AR), a typical GPCR with a high affinity for adenosine, was expressed in many immune cells, such as regulatory T cells, cytotoxic T cells, macrophages, etc. Adenosine binding to the A2AR receptor activates the typical G protein and triggers the cAMP/PKA/CREB pathway. The adenosine-A2AR pathway plays an important role in protecting normal organs and tissues from the autoimmune response of immune cells. However, many solid tumors hijack the adenosine-A2AR pathway by promoting adenosine accumulation. The activation of the A2AR pathway inhibited the immune response of immune cells and then promotes the immune escape of tumor cells in the tumor microenvironment. Recently, both animal experiments and clinical trials indicated that blocking the adenosine pathway can inhibit the progression of a variety of solid tumors. In addition, it is encouraging that A2AR blockade combined with CAR T cells therapy showed better anti-tumor efficacy. Therefore, this review will discuss the role of the adenosine-A2AR pathway in the tumor microenvironment and summarize recent advances of A2AR-cancer related studies.
A2A受体(A2AR)是一种对腺苷具有高亲和力的典型G蛋白偶联受体(GPCR),在许多免疫细胞中表达,如调节性T细胞、细胞毒性T细胞、巨噬细胞等。腺苷与A2AR受体结合会激活典型的G蛋白并触发cAMP/PKA/CREB信号通路。腺苷 - A2AR信号通路在保护正常器官和组织免受免疫细胞的自身免疫反应方面发挥着重要作用。然而,许多实体瘤通过促进腺苷积累来利用腺苷 - A2AR信号通路。A2AR信号通路的激活会抑制免疫细胞的免疫反应,进而促进肿瘤微环境中肿瘤细胞的免疫逃逸。最近,动物实验和临床试验均表明,阻断腺苷信号通路可以抑制多种实体瘤的进展。此外,令人鼓舞的是,A2AR阻断与嵌合抗原受体(CAR)T细胞疗法联合使用显示出更好的抗肿瘤疗效。因此,本综述将讨论腺苷 - A2AR信号通路在肿瘤微环境中的作用,并总结A2AR与癌症相关研究的最新进展。