Molecular and Clinical Analysis of Predictive Biomarkers in Non-Small-Cell Lung Cancer

被引:10
|
作者
Passaro, A. [1 ]
Palazzo, A. [1 ]
Trenta, P. [1 ]
Mancini, M. L. [1 ]
Morano, F. [1 ]
Cortesi, E. [1 ]
机构
[1] Univ Roma La Sapienza, Div Med Oncol, I-00161 Rome, Italy
关键词
ALK; BRCA1; c-MET; EGFR; ERCC1; KRAS; NSCLC; predictive biomarkers; EPIDERMAL-GROWTH-FACTOR; MESSENGER-RNA EXPRESSION; GENE COPY NUMBER; CISPLATIN PLUS GEMCITABINE; RECEPTOR TYROSINE KINASE; EML4-ALK FUSION GENE; PHASE-III TRIAL; THYMIDYLATE SYNTHASE; THERAPEUTIC-TARGET; ERCC1; EXPRESSION;
D O I
10.2174/092986712801661149
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Non-small-cell lung cancer (NSCLC) is the leading cause of cancer-specific death in the USA and Europe. Over the last two decades, the pathogenetic mechanisms and the molecular alterations of NSCLC have been investigated more intensively, a number of potential therapeutic targets have been identified and new agents against specific molecular targets have been introduced in the treatment of NSCLC. Acquired abnormalities in the genes encoding RAS, p53, KRAS, EGFR and ALK, are particularly important in this field. Whenever targetable mutations are not found, the research of other genetic abnormalities can be useful to personalize chemotherapy. The attention has been focused, in particular, on the endonuclease excision repair cross-complementing1 and BRCA1 status. The use of antimetabolite drugs and the level of expression of their cellular targets seem to be correlated and influence the clinical efficacy of those agents. This review will focus on the role of predictive biomarkers for the treatment of non-small cell lung cancer.
引用
收藏
页码:3689 / 3700
页数:12
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