创新链/学科链/研发链/产业链

新药研发前沿动态 / 医药领域趋势进展

HE Jiacheng, CHENG Zhiyuan, YANG Xinyu, XIAO Jing, ZHANG Lu, LIU Mingyao, LU Weiqiang. Clinical Research Progress of Drugs Targeting Metabolite-Sensing G Protein-Coupled Receptors for Tumor ImmunotherapyJ. Progress in Pharmaceutical Sciences, 2026, 50(8): 701-712. DOI: 10.20053/j.issn1001-5094.202604300419
Citation: HE Jiacheng, CHENG Zhiyuan, YANG Xinyu, XIAO Jing, ZHANG Lu, LIU Mingyao, LU Weiqiang. Clinical Research Progress of Drugs Targeting Metabolite-Sensing G Protein-Coupled Receptors for Tumor ImmunotherapyJ. Progress in Pharmaceutical Sciences, 2026, 50(8): 701-712. DOI: 10.20053/j.issn1001-5094.202604300419

Clinical Research Progress of Drugs Targeting Metabolite-Sensing G Protein-Coupled Receptors for Tumor Immunotherapy

  • G protein-coupled receptors (GPCRs), the largest family of transmembrane signal transducers in human genome, play pivotal regulatory roles in the initiation and progression of major diseases including cancer. Recent studies have shown that metabolitesensing GPCRs can specifically recognize and respond to various tumor-associated metabolites, thereby activating immunosuppressive signals, and further inducing tumor immune escape and drug resistance, rendering them frontier targets in the field of tumor immunotherapy. This review elucidates the mechanisms by which metabolite-sensing GPCRs represented by prostaglandin and adenosine receptors drive tumor immune escape. Meanwhile, it summarizes the key achievements in drug development and the latest clinical research progress targeting these two types of receptors, and conducts in-depth analysis of the opportunities and challenges faced by such targeting drugs in the process of clinical translation, so as to provide new perspectives and insights for the development of nextgeneration tumor immunotherapeutic agents.
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