Raymond Jérémy H, Aktary Zackie, Larue Lionel, Delmas Véronique
Institut Curie, Université PSL, CNRS UMR3347, Inserm U1021, Normal and Pathological Development of Melanocytes, 91400 Orsay, France.
Université Paris-Saclay, CNRS UMR3347, Inserm U1021, Signalisation Radiobiologie et Cancer, 91400 Orsay, France.
Cancers (Basel). 2022 Jan 29;14(3):706. doi: 10.3390/cancers14030706.
G-protein-coupled receptors (GPCRs) serve prominent roles in melanocyte lineage physiology, with an impact at all stages of development, as well as on mature melanocyte functions. GPCR ligands are present in the skin and regulate melanocyte homeostasis, including pigmentation. The role of GPCRs in the regulation of pigmentation and, consequently, protection against external aggression, such as ultraviolet radiation, has long been established. However, evidence of new functions of GPCRs directly in melanomagenesis has been highlighted in recent years. GPCRs are coupled, through their intracellular domains, to heterotrimeric G-proteins, which induce cellular signaling through various pathways. Such signaling modulates numerous essential cellular processes that occur during melanomagenesis, including proliferation and migration. GPCR-associated signaling in melanoma can be activated by the binding of paracrine factors to their receptors or directly by activating mutations. In this review, we present melanoma-associated alterations of GPCRs and their downstream signaling and discuss the various preclinical models used to evaluate new therapeutic approaches against GPCR activity in melanoma. Recent striking advances in our understanding of the structure, function, and regulation of GPCRs will undoubtedly broaden melanoma treatment options in the future.
G蛋白偶联受体(GPCRs)在黑素细胞谱系生理学中发挥着重要作用,对黑素细胞发育的各个阶段以及成熟黑素细胞的功能均有影响。GPCR配体存在于皮肤中,可调节黑素细胞稳态,包括色素沉着。长期以来,GPCRs在调节色素沉着以及抵御紫外线等外部侵害方面的作用已得到证实。然而,近年来,GPCRs直接在黑色素瘤发生过程中的新功能证据受到了关注。GPCRs通过其细胞内结构域与异源三聚体G蛋白偶联,后者通过各种途径诱导细胞信号传导。这种信号传导调节黑色素瘤发生过程中出现的众多重要细胞过程,包括增殖和迁移。黑色素瘤中与GPCR相关的信号传导可通过旁分泌因子与其受体结合或直接通过激活突变来激活。在本综述中,我们介绍了与黑色素瘤相关的GPCRs改变及其下游信号传导,并讨论了用于评估针对黑色素瘤中GPCR活性的新治疗方法的各种临床前模型。我们对GPCRs的结构、功能和调节的理解最近取得的显著进展无疑将在未来拓宽黑色素瘤的治疗选择。