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c-Met:结构、功能及治疗性抑制的潜力

c-Met: structure, functions and potential for therapeutic inhibition.

作者信息

Ma Patrick C, Maulik Gautam, Christensen James, Salgia Ravi

机构信息

Department of Medical Oncology, Lowe Center for Thoracic Oncology, Dana-Farber Cancer Institute, Brigham and Women's Hospital, and Harvard Medical School, 44 Binney Street, Boston, MA 02115, USA.

出版信息

Cancer Metastasis Rev. 2003 Dec;22(4):309-25. doi: 10.1023/a:1023768811842.

Abstract

Studies on signal transduction pathways have generated various promising molecular targets for therapeutic inhibition in cancer therapy. Receptor tyrosine kinases represent an important class of such therapeutic targets. c-Met is a receptor tyrosine kinase that has been shown to be overexpressed and/or mutated in a variety of malignancies. A number of c-Met activating mutations, many of which are located in the tyrosine kinase domain, have been detected in various solid tumors and have been implicated in invasion and metastasis of tumor cells. It is known that stimulation of c-Met via its natural ligand, hepatocyte growth factor (also known as scatter factor, HGF/SF) results in a plethora of biological and biochemical effects in the cell. Activation of c-Met signaling can lead to scattering, angiogenesis, proliferation, enhanced cell motility, invasion, and eventual metastasis. In this review, the role of c-Met dysregulation in tumor progression and metastasis is discussed in detail with particular emphasis on c-Met mutations. Moreover, we summarize current knowledge on various pathways of c-Met signal transduction, highlighting the central role in the cytoskeletal functions. In this summary is included recent data in our laboratory indicating that phosphorylation of focal adhesion proteins, such as paxillin, p125FAK, and PYK2, occurs in response to c-Met stimulation in lung cancer cells. Most importantly, current data on c-Met suggest that when mutated or overexpressed in malignant cells, c-Met would serve as an important therapeutic target.

摘要

信号转导通路的研究已产生了多种有望用于癌症治疗中进行治疗性抑制的分子靶点。受体酪氨酸激酶是这类治疗靶点中的重要一类。c-Met是一种受体酪氨酸激酶,已证实在多种恶性肿瘤中存在过表达和/或突变。在各种实体瘤中已检测到许多c-Met激活突变,其中许多位于酪氨酸激酶结构域,并且这些突变与肿瘤细胞的侵袭和转移有关。已知通过其天然配体肝细胞生长因子(也称为分散因子,HGF/SF)刺激c-Met会在细胞中产生大量生物学和生化效应。c-Met信号的激活可导致细胞分散、血管生成、增殖、细胞运动性增强、侵袭以及最终的转移。在本综述中,将详细讨论c-Met失调在肿瘤进展和转移中的作用,尤其着重于c-Met突变。此外,我们总结了关于c-Met信号转导各种途径的现有知识,强调其在细胞骨架功能中的核心作用。本综述纳入了我们实验室的最新数据,这些数据表明,在肺癌细胞中,桩蛋白、p125FAK和PYK2等粘着斑蛋白的磷酸化是对c-Met刺激的响应。最重要的是,关于c-Met的现有数据表明,当在恶性细胞中发生突变或过表达时,c-Met将成为一个重要的治疗靶点。

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