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使用蛋白质-蛋白质相互作用抑制剂靶向粘着斑激酶

Targeting Focal Adhesion Kinase Using Inhibitors of Protein-Protein Interactions.

作者信息

Mousson Antoine, Sick Emilie, Carl Philippe, Dujardin Denis, De Mey Jan, Rondé Philippe

机构信息

Faculté de Pharmacie, Université de Strasbourg, 67401 Illkirch, France.

CNRS UMR 7021, Laboratoire de Bioimagerie et Pathologies, 67401 Illkirch, France.

出版信息

Cancers (Basel). 2018 Aug 21;10(9):278. doi: 10.3390/cancers10090278.

Abstract

Focal adhesion kinase (FAK) is a cytoplasmic non-receptor protein tyrosine kinase that is overexpressed and activated in many human cancers. FAK transmits signals to a wide range of targets through both kinase-dependant and independent mechanism thereby playing essential roles in cell survival, proliferation, migration and invasion. In the past years, small molecules that inhibit FAK kinase function have been developed and show reduced cancer progression and metastasis in several preclinical models. Clinical trials have been conducted and these molecules display limited adverse effect in patients. FAK contain multiple functional domains and thus exhibit both important scaffolding functions. In this review, we describe the major FAK interactions relevant in cancer signalling and discuss how such knowledge provide rational for the development of Protein-Protein Interactions (PPI) inhibitors.

摘要

粘着斑激酶(FAK)是一种细胞质非受体蛋白酪氨酸激酶,在许多人类癌症中过表达并被激活。FAK通过激酶依赖性和非依赖性机制将信号传递给广泛的靶点,从而在细胞存活、增殖、迁移和侵袭中发挥重要作用。在过去几年中,已开发出抑制FAK激酶功能的小分子,在多个临床前模型中显示出癌症进展和转移减缓。已经进行了临床试验,这些分子在患者中显示出有限的不良反应。FAK包含多个功能域,因此具有重要的支架功能。在本综述中,我们描述了与癌症信号传导相关的主要FAK相互作用,并讨论了这些知识如何为蛋白质-蛋白质相互作用(PPI)抑制剂的开发提供理论依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf9b/6162372/ef713e3abb3c/cancers-10-00278-g001.jpg

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