Anti-EGFR and ErbB-2 antibodies attenuate cyclooxygenase-2 expression and cooperatively inhibit survival of human colon cancer cells

被引:16
|
作者
Half, Elizabeth
Sun, Yunjie
Sinicrope, Frank A.
机构
[1] Univ Texas, MD Anderson Canc Ctr, Dept Gastrointestinal Med & Nutr, Houston, TX 77030 USA
[2] Mayo Clin, Coll Med, Div Gastroenterol & Hepatol, Rochester, MN 55905 USA
[3] Mayo Clin, Coll Med, Div Oncol, Rochester, MN 55905 USA
关键词
EGFR; ErbB-2; COX-2; NS-398; cetuximab; trastuzumab;
D O I
10.1016/j.canlet.2006.11.020
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cyclooxygenase-2 (COX-2) is a transcriptional target and downstream effector of the ErbB-1 (EGFR) and ErbB-2 signaling pathways. We found that anti-EGFR and anti-ErbB-2 antibodies inhibited ERK phosphorylation and downregulated COX-2 protein expression in HCA-7 human colon carcinoma cells. Both antibodies also augmented the cytotoxic effects of the selective COX-2 inhibitor, NS-398. Inhibition of EGFR and ErbB-2 attenuated cell growth by increasing cell death, and the antibody combination suppressed cell growth to a greater extent than did either antibody alone. In conclusion, EGFR and ErbB-2 regulate ERK-mediated COX-2 expression and their selective inhibition enhanced NS-398-induced cell death. Cooperative inhibition of cell growth by EGFR and ErbB-2 blockade suggests the therapeutic potential of targeting multiple ErbB receptors. (C) 2006 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:237 / 246
页数:10
相关论文
共 50 条
  • [1] Potential role of ERBB-2 and cyclooxygenase-2 expression in human colon carcinomas.
    Antonacopoulou, A.
    Tsamandas, A.
    Skopa, C.
    Bonikos, D.
    Kalofonos, H.
    JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (18) : 172S - 172S
  • [2] The potential role of ERBB-2 and cyclooxygenase-2 expression in human colon carcinoma and risk conditions
    Tsamandas, AC
    Ravazoula, P
    Kourelis, T
    Kalogeropoulou, C
    Petsas, T
    Kardamakis, D
    Bonikos, D
    Kalofonos, H
    LABORATORY INVESTIGATION, 2003, 83 (01) : 135A - 135A
  • [3] The potential role of ERBB-2 and cyclooxygenase-2 expression in human colon carcinoma and risk conditions
    Tsamandas, AC
    Ravazoula, P
    Kourelis, T
    Kalogeropoulou, C
    Petsas, T
    Kardamakis, D
    Bonikos, D
    Kalofonos, H
    MODERN PATHOLOGY, 2003, 16 (01) : 135A - 135A
  • [4] ErbB4 promotes cyclooxygenase-2 expression and cell survival in colon epithelial cells
    Frey, Mark R.
    Hilliard, Valda C.
    Mullane, Matthew T.
    Polk, D. Brent
    LABORATORY INVESTIGATION, 2010, 90 (10) : 1415 - 1424
  • [5] Cyclooxygenase-2 expression in human colon cancer cells increases metastatic potential
    Tsujii, M
    Kawano, S
    DuBois, RN
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (07) : 3336 - 3340
  • [6] EGFR/HER-2 receptor blockade attenuate ERK-mediated cyclooxygenase-2 expression and augment NSAID-induced apoptosis in human colon cancer cells
    Half, E
    Freeburg, E
    Sun, Y
    Sinicrope, F
    GASTROENTEROLOGY, 2005, 128 (04) : A479 - A479
  • [7] Somatostatin modulates both cyclooxygenase-2 expression and proliferation in human colon cancer cells
    Colucci, R
    Blandizzi, C
    Tanini, M
    Ghisu, N
    Breschi, MC
    Del Tacca, M
    GASTROENTEROLOGY, 2003, 124 (04) : A100 - A100
  • [8] ERBB-2 overexpression and cyclooxygenase-2 up-regulation in human cholangiocarcinoma and risk conditions
    Endo, K
    Yoon, BI
    Pairojkul, C
    Demetris, AJ
    Sirica, AE
    HEPATOLOGY, 2002, 36 (02) : 439 - 450
  • [9] Reduction of intracellular pH inhibits constitutive expression of cyclooxygenase-2 in human colon cancer cells
    Pirkebner, D
    Fuetsch, M
    Wittmann, W
    Weiss, H
    Haller, T
    Schramek, H
    Margreiter, R
    Amberger, A
    JOURNAL OF CELLULAR PHYSIOLOGY, 2004, 198 (02) : 295 - 301
  • [10] Chrysin induces apoptosis in different cyclooxygenase-2 (COX-2) expression human colon cancer cells
    Chen, J-N
    Wu, M-S
    Lien, G-S
    Chen, Y-F
    Cheng, Y-S
    Chen, Y-C
    JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2009, 24 : A77 - A77