Molecular Pharmacology Group, Institute of Neuroscience and Psychology, College of Medical, Veterinary and Life Sciences, University of Glasgow Glasgow, UK.
Front Endocrinol (Lausanne). 2011 Nov 9;2:68. doi: 10.3389/fendo.2011.00068. eCollection 2011.
G protein-coupled receptors (GPCRs) remain the best studied class of cell surface receptors and the most tractable family of proteins for novel small molecule drug discovery. Despite this, a considerable number of GPCRs remain poorly characterized and in a significant number of cases, endogenous ligand(s) that activate them remain undefined or are of questionable physiological relevance. GPR35 was initially discovered over a decade ago but has remained an "orphan" receptor. Recent publications have highlighted novel ligands, both endogenously produced and synthetic, which demonstrate significant potency at this receptor. Furthermore, evidence is accumulating which highlights potential roles for GPR35 in disease and therefore, efforts to characterize GPR35 more fully and develop it as a novel therapeutic target in conditions that range from diabetes and hypertension to asthma are increasing. Recently identified ligands have shown marked species selective properties, indicating major challenges for future drug development. As we begin to understand these issues, the continuing efforts to identify novel agonist and antagonist ligands for GPR35 will help to decipher its true physiological relevance; translating multiple assay systems in vitro, to animal disease systems in vivo and finally to man.
G 蛋白偶联受体(GPCRs)仍然是研究最为透彻的细胞表面受体类别,也是新型小分子药物发现中最易于处理的蛋白质家族。尽管如此,仍有相当数量的 GPCRs 特征描述不足,在许多情况下,激活它们的内源性配体仍未确定或具有可疑的生理相关性。GPR35 最初是在十多年前发现的,但一直是一个“孤儿”受体。最近的出版物强调了新型配体,包括内源性和合成的配体,这些配体在该受体上具有显著的效力。此外,越来越多的证据表明 GPR35 在疾病中的潜在作用,因此,人们越来越努力地更全面地描述 GPR35,并将其开发为从糖尿病和高血压到哮喘等疾病的新型治疗靶点。最近确定的配体显示出明显的物种选择性特性,这表明未来药物开发面临重大挑战。随着我们开始理解这些问题,继续努力为 GPR35 鉴定新型激动剂和拮抗剂配体将有助于阐明其真正的生理相关性;将多种体外检测系统转化为体内动物疾病系统,最终转化为人类。