Suppr超能文献

整合素信号衔接蛋白:癌症故事中的不只是配角。

Integrin signalling adaptors: not only figurants in the cancer story.

机构信息

Molecular Biotechnology Centre and Department of Genetics, Biology and Biochemistry, University of Torino, Via Nizza 52, Torino 10126, Italy.

出版信息

Nat Rev Cancer. 2010 Dec;10(12):858-70. doi: 10.1038/nrc2967. Epub 2010 Nov 24.

Abstract

Current evidence highlights the ability of adaptor (or scaffold) proteins to create signalling platforms that drive cellular transformation upon integrin-dependent adhesion and growth factor receptor activation. The understanding of the biological effects that are regulated by these adaptors in tumours might be crucial for the identification of new targets and the development of innovative therapeutic strategies for human cancer. In this Review we discuss the relevance of adaptor proteins in signalling that originates from integrin-mediated cell-extracellular matrix (ECM) adhesion and growth factor stimulation in the context of cell transformation and tumour progression. We specifically underline the contribution of p130 Crk-associated substrate (p130CAS; also known as BCAR1), neural precursor cell expressed, developmentally down-regulated 9 (NEDD9; also known as HEF1), CRK and the integrin-linked kinase (ILK)-pinch-parvin (IPP) complex to cancer, along with the more recently identified p140 Cas-associated protein (p140CAP; also known as SRCIN1).

摘要

目前的证据强调了衔接蛋白(或支架蛋白)在整合素依赖性黏附和生长因子受体激活后,形成信号平台以驱动细胞转化的能力。了解这些衔接蛋白在肿瘤中调控的生物学效应,对于鉴定新的靶点和开发针对人类癌症的创新性治疗策略可能至关重要。在这篇综述中,我们讨论了衔接蛋白在信号转导中的相关性,这些信号转导源于整合素介导的细胞-细胞外基质(ECM)黏附和生长因子刺激,涉及细胞转化和肿瘤进展。我们特别强调了 p130 Crk 相关底物(p130CAS;也称为 BCAR1)、神经前体细胞表达的发育下调 9(NEDD9;也称为 HEF1)、CRK 和整合素连接激酶(ILK)-夹-parvin(IPP)复合物在癌症中的作用,以及最近发现的 p140 Cas 相关蛋白(p140CAP;也称为 SRCIN1)。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验