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TIPE3 是胶质母细胞瘤中细胞凋亡的调节因子。

TIPE3 is a regulator of cell apoptosis in glioblastoma.

机构信息

Department of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, Hubei, 430060, PR China; Central Laboratory, Renmin Hospital of Wuhan University, Wuhan, Hubei, 430060, PR China.

Department of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, Hubei, 430060, PR China; Department of Neurosurgery, Huzhou Central Hospital, Huzhou, Zhejiang, 313000, PR China.

出版信息

Cancer Lett. 2019 Apr 1;446:1-14. doi: 10.1016/j.canlet.2018.12.019. Epub 2019 Jan 11.

Abstract

Tumor necrosis factor alpha-induced protein 8-like 3 (TIPE3) is closely related to tumourigenesis and development. However, its role in human glioblastoma (GBM) and the underlying mechanisms remain unclear. In this study, we demonstrate that TIPE3 is upregulated in GBM, and its high expression predicts poor prognosis. TIPE3 depletion induces GBM cell apoptosis both in vitro and in vivo. Mechanism studies reveal that TIPE3 inhibits p38 phosphorylation and negatively regulates the p38 MAPK pathway. TIPE3 associates with p38. The nuclear translocation of p38 is blocked by TIPE3 overexpression. And p38 phosphorylation could regulate TIPE3-mediated p38 nuclear-cytopalsmic translocation but does not affect TIPE3-p38 association. Rescue experiments confirm that TIPE3 inhibits GBM cell apoptosis via the p38 MAPK pathway. In conclusion, TIPE3 inhibits p38 phosphorylation and blocks p38 nuclear translocation. This action thus negatively regulates the p38 MAPK pathway and results in GBM cell survival.

摘要

肿瘤坏死因子-α诱导蛋白 8 样 3(TIPE3)与肿瘤的发生和发展密切相关。然而,其在人类脑胶质瘤(GBM)中的作用及其潜在机制尚不清楚。在本研究中,我们证明 TIPE3 在 GBM 中上调,其高表达预示着不良预后。TIPE3 耗竭可在体外和体内诱导 GBM 细胞凋亡。机制研究表明,TIPE3 抑制 p38 磷酸化并负调控 p38 MAPK 通路。TIPE3 与 p38 结合。TIPE3 过表达可阻断 p38 的核转位。p38 磷酸化可调节 TIPE3 介导的 p38 核质转位,但不影响 TIPE3-p38 结合。挽救实验证实,TIPE3 通过 p38 MAPK 通路抑制 GBM 细胞凋亡。总之,TIPE3 抑制 p38 磷酸化并阻止 p38 核转位。这种作用负调控 p38 MAPK 通路,导致 GBM 细胞存活。

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