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磷酸肌醇 3-激酶调节亚基 p85α 通过负向调控生长因子信号转导发挥肿瘤抑制作用。

The phosphoinositide 3-kinase regulatory subunit p85alpha can exert tumor suppressor properties through negative regulation of growth factor signaling.

机构信息

Joslin Diabetes Center and Department of Pathology, Harvard Medical School, Boston, Massachusetts 02215, USA.

出版信息

Cancer Res. 2010 Jul 1;70(13):5305-15. doi: 10.1158/0008-5472.CAN-09-3399. Epub 2010 Jun 8.

DOI:10.1158/0008-5472.CAN-09-3399
PMID:20530665
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3204358/
Abstract

Phosphoinositide 3-kinase (PI3K) plays a critical role in tumorigenesis, and the PI3K p85 regulatory subunit exerts both positive and negative effects on signaling. Expression of Pik3r1, the gene encoding p85, is decreased in human prostate, lung, ovarian, bladder, and liver cancers, consistent with the possibility that p85 has tumor suppressor properties. We tested this hypothesis by studying mice with a liver-specific deletion of the Pik3r1 gene. These mice exhibited enhanced insulin and growth factor signaling and progressive changes in hepatic pathology, leading to the development of aggressive hepatocellular carcinomas with pulmonary metastases. Liver tumors that arose exhibited markedly elevated levels of phosphatidylinositol (3,4,5)-trisphosphate, along with Akt activation and decreased PTEN expression, at both the mRNA and protein levels. Together, these results substantiate the concept that the p85 subunit of PI3K has a tumor-suppressive role in the liver and possibly other tissues.

摘要

磷酸肌醇 3-激酶(PI3K)在肿瘤发生中起着关键作用,PI3K p85 调节亚基对信号传递既有正向作用,也有负向作用。编码 p85 的 Pik3r1 基因在人类前列腺癌、肺癌、卵巢癌、膀胱癌和肝癌中的表达降低,这与 p85 具有肿瘤抑制特性的可能性一致。我们通过研究肝脏特异性缺失 Pik3r1 基因的小鼠来检验这一假设。这些小鼠表现出增强的胰岛素和生长因子信号传递,并伴有肝病理的进行性变化,导致具有肺转移的侵袭性肝细胞癌的发展。出现的肝肿瘤表现出明显升高的磷脂酰肌醇(3,4,5)-三磷酸水平,以及 Akt 激活和 PTEN 表达降低,在 mRNA 和蛋白质水平上均如此。综上所述,这些结果证实了 PI3K 的 p85 亚基在肝脏中具有肿瘤抑制作用,可能在其他组织中也是如此。

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