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KRAS 致癌基因在非小细胞肺癌中的临床治疗:一个老靶点的新视角。

KRAS oncogene in non-small cell lung cancer: clinical perspectives on the treatment of an old target.

机构信息

Department of Oncology, Clínica Universidad de Navarra, 31008, Pamplona, Spain.

Program of Solid Tumors and Biomarkers, Center for Applied Medical Research, Pamplona, Spain.

出版信息

Mol Cancer. 2018 Feb 19;17(1):33. doi: 10.1186/s12943-018-0789-x.

Abstract

Lung neoplasms are the leading cause of death by cancer worldwide. Non-small cell lung cancer (NSCLC) constitutes more than 80% of all lung malignancies and the majority of patients present advanced disease at onset. However, in the last decade, multiple oncogenic driver alterations have been discovered and each of them represents a potential therapeutic target. Although KRAS mutations are the most frequently oncogene aberrations in lung adenocarcinoma patients, effective therapies targeting KRAS have yet to be developed. Moreover, the role of KRAS oncogene in NSCLC remains unclear and its predictive and prognostic impact remains controversial. The study of the underlying biology of KRAS in NSCLC patients could help to determine potential candidates to evaluate novel targeted agents and combinations that may allow a tailored treatment for these patients. The aim of this review is to update the current knowledge about KRAS-mutated lung adenocarcinoma, including a historical overview, the biology of the molecular pathways involved, the clinical relevance of KRAS mutations as a prognostic and predictive marker and the potential therapeutic approaches for a personalized treatment of KRAS-mutated NSCLC patients.

摘要

肺癌是全球癌症死亡的主要原因。非小细胞肺癌(NSCLC)占所有肺癌的 80%以上,大多数患者在发病时已处于晚期疾病。然而,在过去十年中,已经发现了多种致癌驱动基因改变,每一种都代表了一个潜在的治疗靶点。尽管 KRAS 突变是肺腺癌患者中最常见的癌基因异常,但针对 KRAS 的有效治疗方法尚未开发。此外,KRAS 癌基因在 NSCLC 中的作用尚不清楚,其预测和预后影响仍存在争议。研究 NSCLC 患者中 KRAS 的潜在生物学特性有助于确定潜在的候选者,以评估可能为这些患者提供针对性治疗的新型靶向药物和联合治疗。本文综述的目的是更新关于 KRAS 突变肺腺癌的最新知识,包括历史概述、涉及的分子通路的生物学、KRAS 突变作为预后和预测标志物的临床相关性以及针对 KRAS 突变 NSCLC 患者进行个体化治疗的潜在治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec42/5817724/d1a051cb615f/12943_2018_789_Fig1_HTML.jpg

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