GPR78 promotes lung cancer cell migration and metastasis by activation of Gαq-Rho GTPase pathway

被引:22
作者
Dong, Dan-Dan [1 ]
Zhou, Hui [2 ]
Li, Gao [3 ]
机构
[1] Sichuan Acad Med Sci, Sichuan Prov Peoples Hosp, Dept Pathol, Chengdu 610072, Sichuan, Peoples R China
[2] Cent S Univ, Xiangya Sch Med, Affiliated Canc Hosp, Dept Thorac Med, Changsha 410013, Hunan, Peoples R China
[3] Hainan Gen Hosp, Thorac Surg, Haikou 570311, Hainan, Peoples R China
关键词
GPR78; Lung cancer; Metastasis; Rho GTPase; PROTEIN-COUPLED RECEPTORS; RAC1 SIGNALING PATHWAYS; ACTIN CYTOSKELETON; FAMILY GTPASES; GPCRS; GPR56; MOTILITY; ADHESION; INVASION;
D O I
10.5483/BMBRep.2016.49.11.133
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
GPR78 is an orphan G-protein coupled receptor (GPCR) that is predominantly expressed in human brain tissues. Currently, the function of GPR78 is unknown. This study revealed that GPR78 was expressed in lung cancer cells and functioned as a novel regulator of lung cancer cell migration and metastasis. We found that knockdown of GPR78 in lung cancer cells suppressed cell migration. Moreover, GPR78 modulated the formation of actin stress fibers in A549 cells, in a RhoA-and Rac1-dependent manner. At the molecular level, GPR78 regulated cell motility through the activation of G alpha q-RhoA/Rac1 pathway. We further demonstrated that in vivo, the knockdown of GPR78 inhibited lung cancer cell metastasis. These findings suggest that GPR78 is a novel regulator for lung cancer metastasis and may serve as a potential drug target against metastatic human lung cancer.
引用
收藏
页码:623 / 628
页数:6
相关论文
共 25 条
[1]   G protein-coupled receptors stimulation and the control of cell migration [J].
Cotton, Mathieu ;
Claing, Audrey .
CELLULAR SIGNALLING, 2009, 21 (07) :1045-1053
[2]   Roles of Rho-family GTPases in cell polarisation and directional migration [J].
Fukata, M ;
Nakagawa, M ;
Kaibuchi, K .
CURRENT OPINION IN CELL BIOLOGY, 2003, 15 (05) :590-597
[3]   mTORC1 and mTORC2 Regulate EMT, Motility, and Metastasis of Colorectal Cancer via RhoA and Rac1 Signaling Pathways [J].
Gulhati, Pat ;
Bowen, Kanika A. ;
Liu, Jianyu ;
Stevens, Payton D. ;
Rychahou, Piotr G. ;
Chen, Min ;
Lee, Eun Y. ;
Weiss, Heidi L. ;
O'Connor, Kathleen L. ;
Gao, Tianyan ;
Evers, B. Mark .
CANCER RESEARCH, 2011, 71 (09) :3246-3256
[4]   Rho GTPases and the actin cytoskeleton [J].
Hall, A .
SCIENCE, 1998, 279 (5350) :509-514
[5]   Rho family GTPases [J].
Hall, Alan .
BIOCHEMICAL SOCIETY TRANSACTIONS, 2012, 40 :1378-1382
[6]   Biochemical and pharmacological control of the multiplicity of coupling at G-protein-coupled receptors [J].
Hermans, E .
PHARMACOLOGY & THERAPEUTICS, 2003, 99 (01) :25-44
[7]   Characterization of GPR56 protein and its suppressed expression in human pancreatic cancer cells [J].
Huang, Yue ;
Fan, Jun ;
Yang, Jing ;
Zhu, Guo-Zhang .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 2008, 308 (1-2) :133-139
[8]   Orphan G protein-coupled receptor GPR56 regulates neural progenitor cell migration via a Gα12/13 and rho pathway [J].
Iguchi, Tokuichi ;
Sakata, Kensei ;
Yoshizaki, Kotaro ;
Tago, Kenji ;
Mizuno, Norikazu ;
Itoh, Hiroshi .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2008, 283 (21) :14469-14478
[9]   Proteasome involvement in the degradation of the Gq family of Gα subunits [J].
Johansson, BB ;
Minsaas, L ;
Aragay, AM .
FEBS JOURNAL, 2005, 272 (20) :5365-5377
[10]   Tissue distribution and functional analyses of the constitutively active orphan G protein coupled receptors, GPR26 and GPR78 [J].
Jones, Philip G. ;
Nawoschik, Stanley P. ;
Sreekumar, Kodangattil ;
Uveges, Albert J. ;
Tseng, Eugene ;
Zhang, Lynn ;
Johnson, Jeremy ;
He, Lan ;
Paulsen, Janet E. ;
Bates, Brian ;
Pausch, Mark H. .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 2007, 1770 (06) :890-901