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针对 NSCLC 治疗的新策略:ERCC1 和 TS 的作用。

New strategies for targeting the therapy of NSCLC: the role of ERCC1 and TS.

机构信息

Department of Clinical and Biological Sciences, University of Turin, Turin, Italy.

出版信息

Adv Med Sci. 2010;55(1):22-5. doi: 10.2478/v10039-010-0017-4.

Abstract

The evaluation of gene and protein expression profiles is a promising strategy to drive the therapeutical decision-making in non-small cell lung cancer (NSCLC). Among the several candidate genes that have been proposed, many retrospective studies have indicated excision repair cross-complementing 1 (ERCC1), an endonuclease responsible for the repair of DNA damages, as a reliable biomarker of tumor sensitivity to platinum-based agents. Moreover, the recent evidences showing the clinical efficacy of next-generation multitargeted antifolate drugs, in NSCLC, have highlighted the role of the determination of thymidylate synthase (TS) expression levels. Here is presented a brief overview of the literature regarding these two genes that are currently under prospective investigation as predictive markers of treatment efficacy in NSCLC.

摘要

基因和蛋白质表达谱的评估是一种很有前途的策略,可以推动非小细胞肺癌(NSCLC)的治疗决策。在提出的几个候选基因中,许多回顾性研究表明,切除修复交叉互补基因 1(ERCC1)是一种负责修复 DNA 损伤的内切酶,是肿瘤对铂类药物敏感性的可靠生物标志物。此外,最近的证据表明,新一代多靶点抗叶酸药物在 NSCLC 中的临床疗效,突显了确定胸苷酸合成酶(TS)表达水平的作用。本文简要综述了这两个基因的文献,目前它们作为 NSCLC 治疗效果的预测标志物正在进行前瞻性研究。

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