Prostaglandin E2 promotes colon cancer cell growth through a Gs-axin-β-catenin signaling axis

被引:743
作者
Castellone, MD
Teramoto, H
Williams, BO
Druey, KM
Gutkind, JS [1 ]
机构
[1] Natl Inst Dent & Craniofacial Res, Oral & Pharyngeal Canc Branch, NIH, Bethesda, MD 20892 USA
[2] Kojin Hosp, Nagoya, Aichi 4638530, Japan
[3] Van Andel Res Inst, Lab Cell Signaling & Carcinogenesis, Grand Rapids, MI 49503 USA
[4] NIAID, Mol Signal Transduct Sect, Lab Allerg Dis, NIH, Rockville, MD 20852 USA
关键词
D O I
10.1126/science.1116221
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
How cyclooxygenase-2 (COX-2) and its proinflammatory metabolite prostaglandin E2 (PGE2) enhance colon cancer progression remains poorly understood. We show that PGE2 stimulates colon cancer cell growth through its heterotrimeric guanine nucleotide-binding protein (G protein)-coupled receptor, EP2, by a signaling route that involves the activation of phosphoinositide 3-kinase and the protein kinase Akt by free G protein beta gamma subunits and the direct association of the G protein a. subunit with the regulator of G protein signaling (RGS) domain of axin. This leads to the inactivation and release of glycogen synthase kinase 3 beta from its complex with axin, thereby relieving the inhibitory phosphorytation of beta-catenin and activating its signaling pathway. These findings may provide a molecular framework for the future evaluation of chemopreventive strategies for colorectal cancer.
引用
收藏
页码:1504 / 1510
页数:7
相关论文
共 40 条
[31]   MITOGEN INACTIVATION OF GLYCOGEN-SYNTHASE KINASE-3-BETA IN INTACT-CELLS VIA SERINE-9 PHOSPHORYLATION [J].
STAMBOLIC, V ;
WOODGETT, JR .
BIOCHEMICAL JOURNAL, 1994, 303 :701-704
[32]   G protein-coupled receptor kinase 2/Gαq/11 interaction -: A novel surface on a regulator of G protein signaling homology domain for binding Gα subunits [J].
Sterne-Marr, R ;
Tesmer, JJG ;
Day, PW ;
Stracquatanio, RP ;
Cilente, JAE ;
O'Connor, KE ;
Pronin, AN ;
Benovic, JL ;
Wedegaertner, PB .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (08) :6050-6058
[33]  
Tanabe S, 2004, METHOD ENZYMOL, V390, P285
[34]   Structure of RGS4 bound to AlF4--activated G(i alpha 1): Stabilization of the transition state for GTP hydrolysis [J].
Tesmer, JJG ;
Berman, DM ;
Gilman, AG ;
Sprang, SR .
CELL, 1997, 89 (02) :251-261
[35]   β-catenin regulates expression of cyclin D1 in colon carcinoma cells [J].
Tetsu, O ;
McCormick, F .
NATURE, 1999, 398 (6726) :422-426
[36]   Combinatorial chemoprevention of intestinal neoplasia [J].
Torrance, CJ ;
Jackson, PE ;
Montgomery, E ;
Kinzler, KW ;
Vogelstein, B ;
Wissner, A ;
Nunes, M ;
Frost, P ;
Discafani, CM .
NATURE MEDICINE, 2000, 6 (09) :1024-1028
[37]   Cancer genes and the pathways they control [J].
Vogelstein, B ;
Kinzler, KW .
NATURE MEDICINE, 2004, 10 (08) :789-799
[38]   Prostaglandin E2 enhances intestinal adenoma growth via activation of the ras-mitogen-activated protein kinase cascade [J].
Wang, DZ ;
Buchanan, FG ;
Wang, HB ;
Dey, SK ;
DuBois, RN .
CANCER RESEARCH, 2005, 65 (05) :1822-1829
[39]   RGS family members: GTPase-activating proteins for heterotrimeric G-protein alpha-subunits [J].
Watson, N ;
Linder, ME ;
Druey, KM ;
Kehrl, JH ;
Blumer, KJ .
NATURE, 1996, 383 (6596) :172-175
[40]   Crystal structure of a β-catenin/axin complex suggests a mechanism for the β-catenin destruction complex [J].
Xing, Y ;
Clements, WK ;
Kimelman, D ;
Xu, WQ .
GENES & DEVELOPMENT, 2003, 17 (22) :2753-2764