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凋亡调节因子1:一种受高度调控的与RASSF1A相互作用的类BH3蛋白。

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

作者信息

Law Jennifer, Yu Victor C, Baksh Shairaz

机构信息

Department of Pediatrics, Faculty of Medicine and Dentistry, University of Alberta, 3055 Katz Group Centre for Pharmacy and Health Research, 113 Street 87 Avenue, Edmonton, AB, Canada T6G 2E1.

出版信息

Mol Biol Int. 2012;2012:536802. doi: 10.1155/2012/536802. Epub 2012 Jun 14.

DOI:10.1155/2012/536802
PMID:22745908
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3382356/
Abstract

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.

摘要

凋亡调节因子1(MOAP-1)是一种类BH3蛋白,在细胞死亡或凋亡的内在和外在模式中均发挥关键作用。MOAP-1是Ras关联结构域家族1A(RASSF1A)/MOAP-1促凋亡外在信号通路的一部分,该通路通过利用肿瘤坏死因子α(TNFα)或肿瘤坏死因子相关凋亡诱导配体(TRAIL)等死亡受体来调节凋亡,从而抑制异常生长。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而发生表观遗传沉默。MOAP-1是RASSF1A的下游效应器,可促进Bax激活和细胞死亡,并且在凋亡过程中受到高度调节。我们推测MOAP-1和RASSF1A是“凋亡检查点”的重要组成部分,直接影响细胞死亡的结果。未能调节这条促凋亡途径可能导致癌症以及其他可能疾病的出现。尽管在人类癌症中经常观察到RASSF1A表达缺失,但目前尚不清楚MOAP-1表达在致癌过程中是否也会受到影响,从而导致恶性生长失控。在本文中,我们将总结关于MOAP-1生物学作用的已知信息以及它作为RASSF1A下游效应器的作用方式。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b95/3382356/2597196b8d39/MBI2012-536802.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b95/3382356/a35fe841cf76/MBI2012-536802.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b95/3382356/7f6dbddf4850/MBI2012-536802.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b95/3382356/ebeb2b8d3043/MBI2012-536802.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b95/3382356/b1c10a7fbe0a/MBI2012-536802.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b95/3382356/2597196b8d39/MBI2012-536802.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b95/3382356/a35fe841cf76/MBI2012-536802.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b95/3382356/7f6dbddf4850/MBI2012-536802.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b95/3382356/ebeb2b8d3043/MBI2012-536802.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b95/3382356/b1c10a7fbe0a/MBI2012-536802.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b95/3382356/2597196b8d39/MBI2012-536802.005.jpg

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