Title Identification of GPR65, a novel regulator of matrix metalloproteinases using high through-put screening
Authors Xu, Hongbo
Chen, Xiaohong
Huang, Junwei
Deng, Weiwei
Zhong, Qi
Yue, Changli
Wang, Pingzhang
Huang, Zhigang
Affiliation Capital Med Univ, Dept Otolaryngol Head & Neck Surg, Beijing Tongren Hosp, Key Lab Otolaryngol Head & Neck Surg, Beijing, Peoples R China.
Peking Univ, Key Lab Med Immunol, Sch Basic Med Sci,Minist Hlth, Dept Immunol,Hlth Sci Ctr,Ctr Human Dis Genom, Beijing 100871, Peoples R China.
Chinese Natl Human Genome Ctr CHGB Beijing, Funct Genom Grp, Beijing, Peoples R China.
Capital Med Univ, Beijing Tongren Hosp, Dept Pathol, Beijing, Peoples R China.
Keywords Matrix metalloproteinases
Gene expression regulation
High through-put screening assay
GPR65
Head and neck cancer
PROTEIN-COUPLED RECEPTORS
SQUAMOUS-CELL CARCINOMA
TUMOR MICROENVIRONMENT
CANCER
EXPRESSION
TDAG8
INVASION
HEAD
Issue Date 2013
Publisher 生物化学与生物物理学研究通讯
Citation BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS.2013,436,(1),96-103.
Abstract Matrix metalloproteinases (MMPs) are over-expressed in nearly all cancers. To study novel regulatory factors of MMP expression in head and neck cancer (HNC), we screened a total of 636 candidate genes encoding putative human transmembrane proteins using MMP promoter reporter in a dual luciferase assay system. Three genes GPR65, AXL and TNERSF10B dramatically activated the induction of MMP3 expression. The induction of MMP expression by GPR65 was further confirmed in A549 and/or FaDu cells. GPR65 mediated MMP induction under acidic conditions. The AP-1 binding site in MMP3 promoter was crucial for MMP3 induction. Moreover, the A549 cells infected by recombinant adenovirus of GPR65 showed accelerated cell invasion. In conclusion, we validate that GPR65 is vital regulatory genes upstream of MMP3, and define a novel mechanism of MMP3 regulation by proton-sensing G-protein-coupled receptors. (C) 2013 Elsevier Inc. All rights reserved.
URI http://hdl.handle.net/20.500.11897/223394
ISSN 0006-291X
DOI 10.1016/j.bbrc.2013.05.065
Indexed SCI(E)
Appears in Collections: 基础医学院

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