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去泛素化酶 OTUD3 调控 PTEN 稳定性并抑制肿瘤发生。

Deubiquitylase OTUD3 regulates PTEN stability and suppresses tumorigenesis.

机构信息

State Key Laboratory of Proteomics, Beijing Proteome Research Center, Beijing Institute of Radiation Medicine, Collaborative Innovation Center for Cancer Medicine, Beijing 100850, China.

Institute of Cancer Stem Cell, Dalian Medical University, Liaoning Province 116044, China.

出版信息

Nat Cell Biol. 2015 Sep;17(9):1169-81. doi: 10.1038/ncb3218. Epub 2015 Aug 17.

Abstract

PTEN is one of the most frequently mutated tumour suppressors and reduction in PTEN protein stability also plays a role in tumorigenesis. Although several ubiquitin ligases for PTEN have been identified, the deubiquitylase for de-polyubiquitylation and stabilization of PTEN is less defined. Here, we report OTUD3 as a deubiquitylase of PTEN. OTUD3 interacts with, de-polyubiquitylates and stabilizes PTEN. Depletion of OTUD3 leads to the activation of Akt signalling, induction of cellular transformation and cancer metastasis. OTUD3 transgenic mice exhibit higher levels of the PTEN protein and are less prone to tumorigenesis. Reduction of OTUD3 expression, concomitant with decreased PTEN abundance, correlates with human breast cancer progression. Furthermore, we identified loss-of-function OTUD3 mutations in human cancers, which either abolish OTUD3 catalytic activity or attenuate the interaction with PTEN. These findings demonstrate that OTUD3 is an essential regulator of PTEN and that the OTUD3-PTEN signalling axis plays a critical role in tumour suppression.

摘要

PTEN 是最常发生突变的肿瘤抑制因子之一,PTEN 蛋白稳定性的降低也在肿瘤发生中起作用。虽然已经鉴定出几种针对 PTEN 的泛素连接酶,但针对去泛素化和稳定 PTEN 的去泛素酶的定义较少。在这里,我们报告 OTUD3 是 PTEN 的去泛素酶。OTUD3 与 PTEN 相互作用、去泛素化并稳定 PTEN。OTUD3 的耗竭会导致 Akt 信号通路的激活、细胞转化和癌症转移的诱导。OTUD3 转基因小鼠表现出更高水平的 PTEN 蛋白,并且不易发生肿瘤形成。OTUD3 表达的减少,同时伴随着 PTEN 丰度的降低,与人类乳腺癌的进展相关。此外,我们在人类癌症中鉴定出功能丧失的 OTUD3 突变,这些突变要么消除 OTUD3 的催化活性,要么削弱与 PTEN 的相互作用。这些发现表明 OTUD3 是 PTEN 的必需调节剂,并且 OTUD3-PTEN 信号轴在肿瘤抑制中起着关键作用。

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