Shanghai Key Laboratory of Regulatory Biology, The Institute of Biomedical Sciences and School of Life Sciences, East China Normal University, Shanghai, 200241, China.
Curr Top Med Chem. 2019;19(16):1464-1483. doi: 10.2174/1568026619666190628115644.
The great clinical success of chimeric antigen receptor T cell (CAR-T) and PD-1/PDL-1 inhibitor therapies suggests the drawing of a cancer immunotherapy age. However, a considerable proportion of cancer patients currently receive little benefit from these treatment modalities, indicating that multiple immunosuppressive mechanisms exist in the tumor microenvironment. In this review, we mainly discuss recent advances in small molecular regulators targeting G Protein-Coupled Receptors (GPCRs) that are associated with oncology immunomodulation, including chemokine receptors, purinergic receptors, prostaglandin E receptor EP4 and opioid receptors. Moreover, we outline how they affect tumor immunity and neoplasia by regulating immune cell recruitment and modulating tumor stromal cell biology. We also summarize the data from recent clinical advances in small molecular regulators targeting these GPCRs, in combination with immune checkpoints blockers, such as PD-1/PDL-1 and CTLA4 inhibitors, for cancer treatments.
嵌合抗原受体 T 细胞(CAR-T)和 PD-1/PDL-1 抑制剂治疗的巨大临床成功表明癌症免疫治疗时代的到来。然而,目前相当一部分癌症患者从这些治疗方式中获益甚微,这表明肿瘤微环境中存在多种免疫抑制机制。在这篇综述中,我们主要讨论了针对与肿瘤免疫调节相关的 G 蛋白偶联受体(GPCR)的小分子调节剂的最新进展,包括趋化因子受体、嘌呤能受体、前列腺素 E 受体 EP4 和阿片受体。此外,我们还概述了它们如何通过调节免疫细胞募集和调节肿瘤基质细胞生物学来影响肿瘤免疫和肿瘤发生。我们还总结了针对这些 GPCR 的小分子调节剂与免疫检查点抑制剂(如 PD-1/PDL-1 和 CTLA4 抑制剂)联合用于癌症治疗的最新临床进展数据。