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人类癌症中的 RAS 突变:精准医学中的作用。

RAS mutations in human cancers: Roles in precision medicine.

机构信息

Department of Molecular Cellular Oncology and Microbiology, Tokyo Medical and Dental University, 1-5-45 Yushima, Bunkyo-ku, Tokyo 113-8549 Japan.

DiSTABiF, Dipartimento di Scienze e Tecnologie Ambientali, Biologiche e Farmaceutiche, Seconda Università di Napoli, via Vivaldi 43, Caserta 81100 Italy.

出版信息

Semin Cancer Biol. 2019 Dec;59:23-35. doi: 10.1016/j.semcancer.2019.06.007. Epub 2019 Jun 27.

Abstract

Ras proteins play a crucial role as a central component of the cellular networks controlling a variety of signaling pathways that regulate growth, proliferation, survival, differentiation, adhesion, cytoskeletal rearrangements and motility of a cell. Almost, 4 decades passed since Ras research was started and ras genes were originally discovered as retroviral oncogenes. Later on, mutations of the human RAS genes were linked to tumorigenesis. Genetic analyses found that RAS is one of the most deregulated oncogenes in human cancers. In this review, we summarize the pioneering works which allowed the discovery of RAS oncogenes, the finding of frequent mutations of RAS in various human cancers, the role of these mutations in tumorigenesis and mutation-activated signaling networks. We further describe the importance of RAS mutations in personalized or precision medicine particularly in molecular targeted therapy, as well as their use as diagnostic and prognostic markers as therapeutic determinants in human cancers.

摘要

Ras 蛋白作为细胞网络的核心组成部分,在控制多种信号通路中发挥着关键作用,这些信号通路调节细胞的生长、增殖、存活、分化、黏附、细胞骨架重排和运动。自 Ras 研究开始以来,已经过去了将近 40 年,ras 基因最初被发现是逆转录病毒致癌基因。后来,人类 RAS 基因的突变与肿瘤发生有关。遗传分析发现,RAS 是人类癌症中最失调的致癌基因之一。在这篇综述中,我们总结了促成 Ras 致癌基因发现的开创性工作,发现 RAS 基因在各种人类癌症中经常发生突变,这些突变在肿瘤发生中的作用以及突变激活的信号网络。我们进一步描述了 RAS 突变在个性化或精准医学中的重要性,特别是在分子靶向治疗中,以及它们作为人类癌症中诊断和预后标志物以及治疗决定因素的用途。

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