Pathogenesis of lung cancer signalling pathways: roadmap for therapies

被引:142
作者
Brambilla, E. [1 ]
Gazdar, A. [2 ]
机构
[1] Univ Grenoble 1, Inst Albert Bonniot, INSERM, CHRU Grenoble Hop Michallon,Dept Pathol,U823, F-38000 Grenoble, France
[2] Univ Texas SW Med Ctr Dallas, Dallas, TX 75390 USA
关键词
Lung cancer pathology; molecular biology; molecular genetics; molecular pathology; molecular therapy; signal pathways; GROWTH-FACTOR RECEPTOR; MITOCHONDRIAL-DNA MUTATIONS; BCL-2 FAMILY PROTEINS; GENE COPY NUMBER; SMALL-CELL; SOMATIC MUTATIONS; TYROSINE KINASE; SUSCEPTIBILITY LOCUS; PROMOTER METHYLATION; BRONCHIAL LESIONS;
D O I
10.1183/09031936.00014009
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Lung cancer is the major cancer killer worldwide, and 5-yr survival is extremely poor (<= 15%), accentuating the need for more effective therapeutic strategies. Significant advances in lung cancer biology may lead to customised therapy based on targeting specific genes and pathways. The main signalling pathways that could provide roadmaps for therapy include the following: growth promoting pathways (Epidermal Growth Factor Receptor/ARF Ras/Phosphatidyllnositol 3-Kinase), growth inhibitory pathways (p53/Rb/P14(ARF), STK11), apoptotic pathways (Bcl-2/Bax/Fas/FasL), DNA repair and immortalisation genes. Epigenetic changes in lung cancer contribute strongly to cell transformation by modifying chromatin structures and the specific expression of genes; these include DNA methylation, histone and chromatin protein modification, and micro-RNA, all of which are responsible for the silencing of tumour suppressor genes while enhancing expression of oncogenes. The genetic and epigenetic pathways involved in lung tumorigenesis differ between smokers and nonsmokers, and are tools for cancer diagnosis, prognosis, clinical follow-up and targeted therapies.
引用
收藏
页码:1485 / 1497
页数:13
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