ERCC1公司
核苷酸切除修复
顺铂
DNA修复
DNA损伤
医学
重组酶
癌症研究
化疗
肿瘤科
基因
生物
内科学
DNA
遗传学
重组
作者
Rafael Rosella,Manuel Cobo,Dolores Isla,José Miguel Sánchez,Miquel Tarón,Giuseppe Altavilla,Mariacarmela Santarpía,Teresa Morán,Sílvia Catot,Olatz Etxaniza
出处
期刊:Lung Cancer
[Elsevier]
日期:2005-12-01
卷期号:50: S33-S40
被引量:42
标识
DOI:10.1016/s0169-5002(05)81571-5
摘要
Cisplatin-based chemotherapy has long been the cornerstone of non-small cell lung cancer (NSCLC) management. However, median survival rarely exceeds 1 year. The identification of molecular markers can help to predict response, leading to a broad implementation of the new concept of customized chemotherapy. ERCC1 is an excision nuclease within the nucleotide excision repair pathway that forms a heterodimer with XPE As a unit, they execute the 5' incision into the DNA strand relative to the site of DNA damage. The 5' excision is the last of several steps that are specific to excision of a platinum DNA lesion. In mouse models, normal ERCC1 function is critical to normal aging and brain development. Numerous studies indicate that ERCC1 influences the repair of platinum DNA damage. We report here our accumulated experience of ERCC1 mRNA expression and outcome in cisplatin-treated NSCLC patients and the preliminary confirmatory data on a prospective ERCC1 mRNA customized docetaxel-cisplatin trial, in which low ERCC1 mRNA levels in the tumor correlate with significantly better response. ERCC1 is one of several proteins involved in the repairosome, where other DNA repair genes, such as BRCA1, are also central to cisplatin resistance.
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