Cancer Center, The First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, Zhejiang, China.
Key Laboratory of Precision Diagnosis and Treatment for Hepatobiliary and Pancreatic Tumor of Zhejiang Province, Hangzhou, Zhejiang, China.
Biomed Res Int. 2018 Oct 17;2018:1823726. doi: 10.1155/2018/1823726. eCollection 2018.
Aberrant expression of G protein-coupled receptors (GPCRs) is frequently associated with tumorigenesis. G Protein-coupled receptor class C group 5 member A (GPRC5A) is a member of the GPCR superfamily, is expressed preferentially in lung tissues, and is regulated by various entities at multiple levels. GPRC5A exerts a tumor suppressive role in lung cancer and GPRC5A deletion promotes lung tumor initiation and progression. Recent advances have highlighted that GPRC5A dysregulation is found in various human cancers and is related to many tumor-associated signaling pathways, including the cyclic adenosine monophosphate (cAMP), nuclear factor (NF)-B, signal transducer and activator of transcription (STAT) 3, and focal adhesion kinase (FAK)/Src signaling. This review aimed to summarize our updated view on the biology and regulation of GPRC5A, its expression in human cancers, and the linked signaling pathways. A better comprehension of the underlying cellular and molecular mechanisms of GPRC5A will provide novel insights into its potential diagnostic and therapeutic value.
G 蛋白偶联受体(GPCRs)的异常表达常与肿瘤发生有关。G 蛋白偶联受体 C 族 5 组 A(GPRC5A)是 GPCR 超家族的一员,在肺组织中优先表达,并受多种实体在多个水平上的调控。GPRC5A 在肺癌中发挥肿瘤抑制作用,GPRC5A 缺失促进肺肿瘤的发生和进展。最近的研究进展强调,GPRC5A 的失调在各种人类癌症中都有发现,并与许多与肿瘤相关的信号通路有关,包括环磷酸腺苷(cAMP)、核因子(NF)-B、信号转导和转录激活因子(STAT)3 以及黏着斑激酶(FAK)/Src 信号通路。本综述旨在总结我们对 GPRC5A 的生物学和调控、其在人类癌症中的表达以及相关信号通路的最新认识。更好地理解 GPRC5A 的细胞和分子机制将为其潜在的诊断和治疗价值提供新的见解。