Suppr超能文献

癌症中的PTEN/PI3K/AKT信号通路及其治疗意义

The PTEN/PI3K/AKT signalling pathway in cancer, therapeutic implications.

作者信息

Carnero Amancio, Blanco-Aparicio Carmen, Renner Oliver, Link Wolfgang, Leal Juan F M

机构信息

Experimental Therapeutics Programme, Spanish National Cancer Centre (CNIO), C/Melchor Fernandez Almagro 3, 28029 Madrid, Spain.

出版信息

Curr Cancer Drug Targets. 2008 May;8(3):187-98. doi: 10.2174/156800908784293659.

Abstract

PTEN/PI3K/AKT constitutes an important pathway regulating the signaling of multiple biological processes such as apoptosis, metabolism, cell proliferation and cell growth. PTEN is a dual protein/lipid phosphatase which main substrate is the phosphatidyl-inositol,3,4,5 triphosphate (PIP3), the product of PI3K. Increase in PIP3 recruits AKT to the membrane where it is activated by other kinases also dependent on PIP3. Many components of this pathway have been described as causal forces in cancer. PTEN activity is lost by mutations, deletions or promoter methylation silencing at high frequency in many primary and metastatic human cancers. Germ line mutations of PTEN are found in several familial cancer predisposition syndromes. Activating mutations which have been reported for PI3K and AKT, in tumours are able to confer tumourigenic properties in several cellular systems. Additionally, the binding of PI3K to oncogenic ras is essential for the transforming properties of ras. In summary, the data strongly support the view of the PTEN/PI3K/AKT pathway as an important target for drug discovery.

摘要

PTEN/PI3K/AKT构成了一条重要通路,可调节多种生物过程的信号传导,如细胞凋亡、代谢、细胞增殖和细胞生长。PTEN是一种双功能蛋白/脂质磷酸酶,其主要底物是磷脂酰肌醇-3,4,5-三磷酸(PIP3),即PI3K的产物。PIP3增加会将AKT募集到细胞膜上,在那里它会被其他同样依赖PIP3的激酶激活。该通路的许多成分已被描述为癌症的致病因素。在许多原发性和转移性人类癌症中,PTEN活性因突变、缺失或启动子甲基化沉默而高频丧失。在几种家族性癌症易感综合征中发现了PTEN的种系突变。在肿瘤中,已报道的PI3K和AKT激活突变能够在多种细胞系统中赋予致瘤特性。此外,PI3K与致癌性Ras的结合对于Ras的转化特性至关重要。总之,这些数据有力地支持了将PTEN/PI3K/AKT通路视为药物研发重要靶点的观点。

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