GPCRs: Emerging anti-cancer drug targets

被引:130
作者
Gutierrez, Ainhoa Nieto [1 ]
McDonald, Patricia H. [1 ]
机构
[1] Scripps Res Inst, Dept Mol Med, 130 Scripps Way, Jupiter, FL 33458 USA
关键词
GPCR; Signalling; Cancer; Drug targets; Drug discovery; PROTEIN-COUPLED RECEPTORS; GROWTH-FACTOR RECEPTOR; BREAST-CANCER; LYSOPHOSPHATIDIC ACID; SPHINGOSINE; 1-PHOSPHATE; SIGNALING PATHWAYS; CELL-PROLIFERATION; BETA-ARRESTIN; FUNCTIONAL SELECTIVITY; MYOCARDIAL-INFARCTION;
D O I
10.1016/j.cellsig.2017.09.005
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
G protein-coupled receptors (GPCRs) constitute the largest and most diverse protein family in the human genome with over 800 members identified to date. They play critical roles in numerous cellular and physiological processes, including cell proliferation, differentiation, neurotransmission, development and apoptosis. Consequently, aberrant receptor activity has been demonstrated in numerous disorders/diseases, and as a result GPCRs have become the most successful drug target class in pharmaceuticals treating a wide variety of indications such as pain, inflammation, neurobiological and metabolic disorders. Many independent studies have also demonstrated a key role for GPCRs in tumourigenesis, establishing their involvement in cancer initiation, progression, and metastasis. Given the growing appreciation of the role(s) that GPCRs play in cancer pathogenesis, it is surprising to note that very few GPCRs have been effectively exploited in pursuit of anti-cancer therapies. The present review provides a broad overview of the roles that various GPCRs play in cancer growth and development, highlighting the potential of pharmacologically modulating these receptors for the development of novel anti-cancer therapeutics.
引用
收藏
页码:65 / 74
页数:10
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