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丝裂原活化蛋白激酶4激酶3(MAP4K3)通过对仅含BH3结构域蛋白的转录后调控来调节细胞死亡。

MAP4K3 modulates cell death via the post-transcriptional regulation of BH3-only proteins.

作者信息

Lam David, Dickens David, Reid Elizabeth B, Loh Samantha H Y, Moisoi Nicoleta, Martins L Miguel

机构信息

Cell Death Regulation Laboratory, Medical Research Council Toxicology Unit, Hodgkin Building, Lancaster Road, Leicester LE1 9HN, United Kingdom.

出版信息

Proc Natl Acad Sci U S A. 2009 Jul 21;106(29):11978-83. doi: 10.1073/pnas.0900608106. Epub 2009 Jul 8.

Abstract

Intracellular signal transduction networks involving protein kinases are important modulators of cell survival and cell death in multicellular organisms. Functional compromise of these networks has been linked to aberrant apoptosis in diseases such as cancer. To identify novel kinase regulators of cell death, we conducted an RNAi-based screen to identify modulators of the intrinsic apoptosis pathway. Using this approach, we identified MAP4K3 as a novel apoptosis inducer. Here, we present evidence that this pro-apoptotic kinase orchestrates activation of BAX via the concerted posttranscriptional modulation of PUMA, BAD, and BIM. Additionally, we found decreased levels of this kinase in pancreatic cancer samples, suggesting a tumor suppressor role for MAP4K3 in pancreatic tumorigenesis.

摘要

涉及蛋白激酶的细胞内信号转导网络是多细胞生物中细胞存活和细胞死亡的重要调节因子。这些网络的功能受损与癌症等疾病中的异常凋亡有关。为了鉴定细胞死亡的新型激酶调节因子,我们进行了一项基于RNA干扰的筛选,以鉴定内源性凋亡途径的调节因子。通过这种方法,我们鉴定出MAP4K3是一种新型凋亡诱导剂。在此,我们提供证据表明,这种促凋亡激酶通过对PUMA、BAD和BIM的协同转录后调节来协调BAX的激活。此外,我们发现胰腺癌样本中这种激酶的水平降低,表明MAP4K3在胰腺肿瘤发生中具有肿瘤抑制作用。

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