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Ras/Raf信号传导与新兴药物治疗靶点。

Ras/Raf signalling and emerging pharmacotherapeutic targets.

作者信息

Kolch Walter

机构信息

The Beatson Institute for Cancer Research, Cancer Research UK Beatson Laboratories, Garscube Estate, Glasgow, UK.

出版信息

Expert Opin Pharmacother. 2002 Jun;3(6):709-18. doi: 10.1517/14656566.3.6.709.

Abstract

The Ras-Raf-MEK-ERK pathway is a ubiquitously expressed signalling module that regulates the proliferation, differentiation and survival of cells. This pathway features several oncogenes and is deregulated in approximately 30% of all human cancers. Thus, it has emerged as a prime target for antitumour therapy. Drugs targeting Ras, Raf or MEK are currently in clinical trials. They comprise vaccines, isoprenylation inhibitors, antisense compounds and kinase inhibitors. Most are remarkably well tolerated and some show promising efficacy. However, it is not clear which components of this pathway should be targeted and how maximum efficacy can be achieved. This paper reviews the current efforts with an emphasis on new mechanistic and conceptual approaches.

摘要

Ras-Raf-MEK-ERK信号通路是一种广泛表达的信号传导模块,可调节细胞的增殖、分化和存活。该信号通路包含多个癌基因,在大约30%的人类癌症中失调。因此,它已成为抗肿瘤治疗的主要靶点。目前,针对Ras、Raf或MEK的药物正在进行临床试验。这些药物包括疫苗、异戊二烯化抑制剂、反义化合物和激酶抑制剂。大多数药物耐受性良好,有些显示出有前景的疗效。然而,尚不清楚该信号通路的哪些组分应作为靶点以及如何实现最大疗效。本文综述了当前的研究工作,重点介绍了新的机制和概念方法。

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