凋亡调节因子1:一个高度调控的rassf1a相互作用bh3样蛋白。

Molecular biology international Pub Date : 2012-01-01 Epub Date: 2012-06-14 DOI:10.1155/2012/536802
Jennifer Law, Victor C Yu, Shairaz Baksh
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引用次数: 20

摘要

凋亡调节因子1 (Modulator of apoptosis 1, MOAP-1)是一种bh3样蛋白,在细胞内源性和外源性死亡或凋亡模式中起关键作用。MOAP-1是Ras关联结构域家族1A (RASSF1A)/MOAP-1促凋亡外源性信号通路的一部分,通过肿瘤坏死因子α (TNFα)或tnf相关凋亡诱导配体(TRAIL)等死亡受体抑制异常生长来调节细胞凋亡。RASSF1A是一种真正的肿瘤抑制基因,在许多人类癌症中通过启动子特异性甲基化被表观遗传沉默。MOAP-1是RASSF1A的下游效应因子,促进Bax活化和细胞死亡,在细胞凋亡过程中受到高度调控。我们推测MOAP-1和RASSF1A是直接影响细胞死亡结果的“凋亡检查点”的重要元素。这种促凋亡通路的调节失败可能导致癌症和其他疾病的出现。虽然在人类癌症中经常观察到RASSF1A表达的缺失,但目前尚不清楚MOAP-1的表达是否也可能在癌变过程中受到影响,从而导致不受控制的恶性生长。在本文中,我们将总结已知的MOAP-1的生物学作用,以及它如何作为RASSF1A的下游效应物发挥作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Modulator of Apoptosis 1: A Highly Regulated RASSF1A-Interacting BH3-Like Protein.

Modulator of apoptosis 1 (MOAP-1) is a BH3-like protein that plays key roles in both the intrinsic and extrinsic modes of cell death or apoptosis. MOAP-1 is part of the Ras association domain family 1A (RASSF1A)/MOAP-1 pro-apoptotic extrinsic signaling pathway that regulates apoptosis by utilizing death receptors such as tumor necrosis factor α (TNFα) or TNF-related apoptosis-inducing ligand (TRAIL) to inhibit abnormal growth. RASSF1A is a bona fide tumor suppressor gene that is epigenetically silenced by promoter-specific methylation in numerous human cancers. MOAP-1 is a downstream effector of RASSF1A that promotes Bax activation and cell death and is highly regulated during apoptosis. We speculate that MOAP-1 and RASSF1A are important elements of an "apoptotic checkpoint" that directly influences the outcome of cell death. The failure to regulate this pro-apoptotic pathway may result in the appearance of cancer and possibly other disorders. Although loss of RASSF1A expression is frequently observed in human cancers, it is currently unknown if MOAP-1 expression may also be affected during carcinogenesis to result in uncontrolled malignant growth. In this article, we will summarize what is known about the biological role(s) of MOAP-1 and how it functions as a downstream effector to RASSF1A.

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