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EB 病毒潜伏膜蛋白 1 通过抑制维 A 酸受体-β₂表达克服全反式维 A 酸诱导的细胞凋亡。

Epstein-Barr Virus latent membrane protein 1 overcomes all-trans retinoic acid-induced apoptosis by inhibiting retinoic acid receptor-β₂ expression.

机构信息

Department of Microbiology, College of Natural Sciences, Pusan National University, Busan 609-735, Republic of Korea.

出版信息

Biochem Biophys Res Commun. 2012 Jun 29;423(2):313-8. doi: 10.1016/j.bbrc.2012.05.118. Epub 2012 May 30.

Abstract

Nasopharyngeal carcinoma is closely associated with infection with Epstein-Barr Virus (EBV); however, the mechanism is still unclear. Here, we report that the EBV oncoprotein, latent membrane protein 1 (LMP1), suppresses apoptotic cell death provoked by all-trans retinoic acid (ATRA) in NPC cells. For this purpose, LMP1 downregulated levels of Bak whilst it upregulated levels of Bcl2, lowering the ratio of Bak to Bcl2. In addition, LMP1 suppressed ATRA-mediated activation of Caspase 9, Caspase 3, and PARP but not Caspase 8 in Ad-AH cells, suggesting that LMP1 acts by blocking the activation of intrinsic apoptosis pathway by ATRA. These effects were almost completely abolished when levels of retinoic acid receptor-β(2) (RAR-β(2)) in the LMP1-expressing cells were recovered by either exogenous gene expression or treatment with a universal DNMT inhibitor, 5-Aza-2'dC, indicating that LMP1 executes its antiapoptotic effects by downregulating levels of RAR-β(2) via DNA methylation.

摘要

鼻咽癌与 Epstein-Barr 病毒(EBV)感染密切相关,但具体机制尚不清楚。在这里,我们报告 EBV 癌蛋白潜伏膜蛋白 1(LMP1)可抑制全反式维甲酸(ATRA)诱导的 NPC 细胞凋亡。为此,LMP1 下调 Bak 的水平,同时上调 Bcl2 的水平,降低 Bak 与 Bcl2 的比值。此外,LMP1 抑制 Ad-AH 细胞中 ATRA 介导的 Caspase 9、Caspase 3 和 PARP 的激活,但不抑制 Caspase 8,表明 LMP1 通过阻断 ATRA 诱导的内在细胞凋亡途径的激活而起作用。当通过外源基因表达或用通用的 DNA 甲基转移酶抑制剂 5-Aza-2'dC 处理恢复 LMP1 表达细胞中的视黄酸受体-β(2)(RAR-β(2))水平时,这些作用几乎完全被消除,表明 LMP1 通过 DNA 甲基化下调 RAR-β(2)水平来执行其抗凋亡作用。

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