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

被引:739
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
  • [1] Mammalian RGS proteins: Barbarians at the gate
    Berman, DM
    Gilman, AG
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (03) : 1269 - 1272
  • [2] COX-2: A molecular target for colorectal cancer prevention
    Brown, JR
    DuBois, RN
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (12) : 2840 - 2855
  • [3] A protein knockdown strategy to study the function of β-catenin in tumorigenesis -: art. no. 10
    Cong, F
    Zhang, JX
    Pao, W
    Zhou, PB
    Varmus, H
    [J]. BMC MOLECULAR BIOLOGY, 2003, 4
  • [4] DUAL EFFECT OF BETA-ADRENERGIC RECEPTORS ON MITOGEN-ACTIVATED PROTEIN-KINASE - EVIDENCE FOR A BETA-GAMMA-DEPENDENT ACTIVATION AND A G-ALPHA(S)-CAMP-MEDIATED INHIBITION
    CRESPO, P
    CACHERO, TG
    XU, NZ
    GUTKIND, JS
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (42) : 25259 - 25265
  • [5] DAY RN, 1989, J BIOL CHEM, V264, P431
  • [6] Differential regulation of glycogen synthase kinase 3β by insulin and Wnt signaling
    Ding, VW
    Chen, RH
    McCormick, F
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (42) : 32475 - 32481
  • [7] Phosphorylation and inactivation of glycogen synthase kinase 3 by protein kinase A
    Fang, XJ
    Yu, SX
    Lu, YL
    Bast, RC
    Woodgett, JR
    Mills, GB
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (22) : 11960 - 11965
  • [8] Phosphorylation of glycogen synthase kinase-3 and stimulation of T-cell factor signaling following activation of EP2 and EP4 prostanoid receptors by prostaglandin E2
    Fujino, H
    West, KA
    Regan, JW
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (04) : 2614 - 2619
  • [9] Hansen-Petrik MB, 2002, CANCER RES, V62, P403
  • [10] Downregulation of β-catenin by human Axin and its association with the APC tumor suppressor, β-catenin and GSK3β
    Hart, MJ
    de los Santos, R
    Albert, IN
    Rubinfeld, B
    Polakis, P
    [J]. CURRENT BIOLOGY, 1998, 8 (10) : 573 - 581