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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.
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页码:237 / 246
页数:10
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