G protein-coupled receptors as promising cancer targets

被引:99
作者
Liu, Ying [1 ]
An, Su [1 ]
Ward, Richard [2 ]
Yang, Yang [1 ]
Guo, Xiao-Xi [1 ]
Li, Wei [3 ]
Xu, Tian-Rui [1 ]
机构
[1] Kunming Univ Sci & Technol, Fac Life Sci & Technol, Kunming 650500, Yunnan, Peoples R China
[2] Univ Glasgow, Coll Med Vet & Life Sci, Inst Mol Cell & Syst Biol, Mol Pharmacol Grp, Glasgow G12 8QQ, Lanark, Scotland
[3] Peoples Hosp Yunnan Prov, Dept Urol, Kidney Canc Res Diag & Translat Technol Ctr Yunna, Kunming 650032, Yunnan, Peoples R China
关键词
GPCR; Cancer; GPR30; Mutation; Activation; GASTRIN-RELEASING-PEPTIDE; GROWTH-FACTOR RECEPTOR; II TYPE-1 RECEPTOR; LYSOPHOSPHATIDIC ACID RECEPTOR; CONVERTING-ENZYME-INHIBITORS; RENIN-ANGIOTENSIN-SYSTEM; MELANOCORTIN; RECEPTOR; FAMILIAL GLUCOCORTICOID DEFICIENCY; MUSCARINIC ACETYLCHOLINE-RECEPTOR; LUTEINIZING-HORMONE RECEPTOR;
D O I
10.1016/j.canlet.2016.03.031
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
G protein-coupled receptors (GPCRs) regulate an array of fundamental biological processes, such as growth, metabolism and homeostasis. Specifically, GPCRs are involved in cancer initiation and progression. However, compared with the involvement of the epidermal growth factor receptor in cancer, that of GPCRs have been largely ignored. Recent findings have implicated many GPCRs in tumorigenesis, tumor progression, invasion and metastasis. Moreover, GPCRs contribute to the establishment and maintenance of a microenvironment which is permissive for tumor formation and growth, including effects upon surrounding blood vessels, signaling molecules and the extracellular matrix. Thus, GPCRs are considered to be among the most useful drug targets against many solid cancers. Development of selective ligands targeting GPCRs may provide novel and effective treatment strategies against cancer and some anticancer compounds are now in clinical trials. Here, we focus on tumor related GPCRs, such as G protein coupled receptor 30, the lysophosphatidic acid receptor, angiotensin receptors 1 and 2, the sphingosine 1-phosphate receptors and gastrin releasing peptide receptor. We also summarize their tissue distributions, activation and roles in tumorigenesis and discuss the potential use of GPCR agonists and antagonists in cancer therapy. (C) 2016 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:226 / 239
页数:14
相关论文
共 329 条
[1]   Activation of mechanosensitive ion channel TRPV4 normalizes tumor vasculature and improves cancer therapy [J].
Adapala, R. K. ;
Thoppil, R. J. ;
Ghosh, K. ;
Cappelli, H. C. ;
Dudley, A. C. ;
Paruchuri, S. ;
Keshamouni, V. ;
Klagsbrun, M. ;
Meszaros, J. G. ;
Chilian, W. M. ;
Ingber, D. E. ;
Thodeti, C. K. .
ONCOGENE, 2016, 35 (03) :314-322
[2]   Expression of P2X7 Receptor Increases In Vivo Tumor Growth [J].
Adinolfi, Elena ;
Raffaghello, Lizzia ;
Giuliani, Anna Lisa ;
Cavazzini, Luigi ;
Capece, Marina ;
Chiozzi, Paola ;
Bianchi, Giovanna ;
Kroemer, Guido ;
Pistoia, Vito ;
Di Virgilio, Francesco .
CANCER RESEARCH, 2012, 72 (12) :2957-2969
[3]   RETRACTED: G-Protein-Coupled Receptor 30 and Estrogen Receptor-α Are Involved in the Proliferative Effects Induced by Atrazine in Ovarian Cancer Cells (Retracted article. See vol. 122, pg. A42, 2014) [J].
Albanito, Lidia ;
Lappano, Rosamaria ;
Madeo, Antonio ;
Chimento, Adele ;
Prossnitz, Eric R. ;
Cappello, Anna Rita ;
Dolce, Vincenza ;
Abonante, Sergio ;
Pezzi, Vincenzo ;
Maggiolini, Marcello .
ENVIRONMENTAL HEALTH PERSPECTIVES, 2008, 116 (12) :1648-1655
[4]  
Allergan Inc, 2012, NOV COMP REC MOD THE
[5]  
Allergan Inc, 2012, NOV OX DER SPHING 1
[6]  
Allergan Inc, 2011, NOV COMP REC MOD THE
[7]   A novel evolutionarily conserved domain of cell-adhesion GPCRs mediates autoproteolysis [J].
Arac, Demet ;
Boucard, Antony A. ;
Bolliger, Marc F. ;
Nguyen, Jenna ;
Soltis, S. Michael ;
Suedhof, Thomas C. ;
Brunger, Axel T. .
EMBO JOURNAL, 2012, 31 (06) :1364-1378
[8]  
Arafat HA, 2007, J AM COLL SURGEONS, V204, P1005
[9]   Antihypertensives as novel antineoplastics: Angiotensin-I-converting enzyme inhibitors and angiotensin II type 1 receptor blockers in pancreatic ductal adenocarcinoma - Discussion [J].
Brennan, Murray F. ;
Riall, Taylor S. ;
Nealon, William H. ;
Arafat, Hwyda A. .
JOURNAL OF THE AMERICAN COLLEGE OF SURGEONS, 2007, 204 (05) :1005-1006
[10]   Angiotensin-induced EGF receptor transactivation inhibits insulin signaling in C9 hepatic cells [J].
Arellano-Plancarte, Araceli ;
Hernandez-Aranda, Judith ;
Catt, Kevin J. ;
Olivares-Reyes, J. Alberto .
BIOCHEMICAL PHARMACOLOGY, 2010, 79 (05) :733-745