Cyclooxygenase-2 and epidermal growth factor receptor: Pharmacologic targets for chemoprevention

被引:349
作者
Dannenberg, AJ
Lippman, SM
Mann, JR
Subbaramaiah, K
DuBois, RN
机构
[1] Vanderbilt Ingram Canc Ctr, Nashville, TN 37232 USA
[2] Cornell Univ, Weill Med Coll, Dept Med, New York, NY USA
[3] Univ Texas, MD Anderson Canc Ctr, Dept Clin Canc Prevent, Houston, TX USA
[4] Univ Texas, MD Anderson Canc Ctr, Dept Thorac Head & Neck Med Oncol, Houston, TX USA
[5] Vanderbilt Univ, Med Ctr, Dept Med, Nashville, TN USA
[6] Vanderbilt Univ, Med Ctr, Dept Canc Biol, Nashville, TN USA
[7] Vanderbilt Univ, Med Ctr, Dept Cell & Dev Biol, Nashville, TN USA
关键词
D O I
10.1200/JCO.2005.09.112
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Understanding the mechanisms underlying carcinogenesis provides insights that are necessary for the development of therapeutic strategies to prevent cancer. Chemoprevention, the use of drugs or natural substances to inhibit carcinogenesis, is a rapidly evolving aspect of cancer research. Evidence is presented that cyclooxygenase-2 (COX-2) and epidermal growth factor receptor (EGFR) are potential pharmacologic targets to prevent cancer. In this paper, we review key data implicating a causal relationship between COX-2, EGFR and carcinogenesis and possible mechanisms of action. We discuss evidence of crosstalk between COX-2 and EGFR in order to strengthen the rationale for combination chemoprevention, and review plans for a clinical trial that will evaluate the concept of combination chemoprevention targeting COX-2 and EGFR.
引用
收藏
页码:254 / 266
页数:13
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