Update on the molecular biology of malignant mesothelioma

被引:77
|
作者
Lee, Amie Y. [1 ]
Raz, Dan J. [1 ]
He, Biad [1 ]
Jablons, David M. [1 ]
机构
[1] Univ Calif San Francisco, Dept Surg, Div Cardiothorac Surg, San Francisco, CA 94143 USA
关键词
mesothelioma; VEGF; EGFR; p16(INK4A); p14(ARF); Wnt; bcl-2; genes;
D O I
10.1002/cncr.22552
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Malignant mesothelioma (MM) is a highly aggressive tumor with a very poor prognosis. The disease is largely unresponsive to conventional chemotherapy or radiotherapy, and most patients die within 10-17 months of the first symptoms. Novel, more effective therapeutic strategies are needed for this inexorably fatal disease. Improvement in our understanding of the molecular biology of MM has identified promising new candidates for targeted treatments. In this review the key molecular signaling pathways, including vascular endothelial growth factor (VEGF), epidermal growth factor (EGF), Wnt, and the cell cycle control genes p53, pRb, and bcl-2 that appear to play an important role in the pathogenesis of MM are explored.
引用
收藏
页码:1454 / 1461
页数:8
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