Targeting the eicosanoid pathway in non-small-cell lung cancer

被引:12
|
作者
Horn, Leora [1 ]
Backlund, Michael [1 ]
Johnson, David H. [1 ]
机构
[1] Vanderbilt Univ, Sch Med, Vanderbilt Ingram Canc Ctr, Div Hematol & Med Oncol, Nashville, TN 37232 USA
关键词
cyclooxygenase-2; eicosanoids; non-small-cell lung cancer; prostaglandin E-2; GROWTH-FACTOR RECEPTOR; PROSTAGLANDIN-E SYNTHASE-1; MAJOR URINARY METABOLITE; PHASE-III TRIAL; SELECTIVE CYCLOOXYGENASE-2 INHIBITOR; VINORELBINE PLUS CISPLATIN; 15-HYDROXYPROSTAGLANDIN DEHYDROGENASE; PROGNOSTIC-SIGNIFICANCE; MESENCHYMAL TRANSITION; COLORECTAL-CANCER;
D O I
10.1517/14728220902915567
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Multiple lines of evidence suggest that cyclooxygenase-2 (COX-2) upregulation is an early event in the development of non-small-cell lung cancer. Preclinical data indicate tumors with upregulation of COX-2 synthesize high levels of prostaglandin E-2 (PGE(2)), which in turn are associated with increased production of proangiogenic factors and enhanced metastatic potential. These findings indicate that an increase in COX-2 expression may play a significant role in the development and growth of lung cancers and possibly with the acquisition of an invasive and metastatic phenotype. Consequently, inhibitors of COX-2 are being studied for their chemopreventative and therapeutic effects in individuals at high risk for lung cancer and patients with established cancers.
引用
收藏
页码:675 / 688
页数:14
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