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ERK5催化非依赖性功能在疾病通路中的意义。

The significance of ERK5 catalytic-independent functions in disease pathways.

作者信息

Le Nhat-Tu

机构信息

Center for Cardiovascular Regeneration, Department of Cardiovascular Sciences, Houston Methodist Research Institute, Houston, TX, United States.

出版信息

Front Cell Dev Biol. 2023 Aug 4;11:1235217. doi: 10.3389/fcell.2023.1235217. eCollection 2023.

DOI:10.3389/fcell.2023.1235217
PMID:37601096
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10436230/
Abstract

Extracellular signal-regulated kinase 5 (ERK5), also known as BMK1 or MAPK7, represents a recent addition to the classical mitogen-activated protein kinase (MAPK) family. This family includes well-known members such as ERK1/2, c-Jun N-terminal kinase (JNK), and p38 mitogen-activated protein kinase (p38 MAPK), as well as atypical MAPKs such as ERK3, ERK4, ERK7 (ERK8), and Nemo-like kinase (NLK). Comprehensive reviews available elsewhere provide detailed insights into ERK5, which interested readers can refer to for in-depth knowledge (Nithianandarajah-Jones et al., 2012; Monti et al., Cancers (Basel), 2022, 14). The primary aim of this review is to emphasize the essential characteristics of ERK5 and shed light on the intricate nature of its activation, with particular attention to the catalytic-independent functions in disease pathways.

摘要

细胞外信号调节激酶5(ERK5),也称为BMK1或MAPK7,是经典丝裂原活化蛋白激酶(MAPK)家族中的新成员。该家族包括著名成员,如ERK1/2、c-Jun氨基末端激酶(JNK)和p38丝裂原活化蛋白激酶(p38 MAPK),以及非典型MAPK,如ERK3、ERK4、ERK7(ERK8)和Nemo样激酶(NLK)。其他地方的综合综述对ERK5有详细的见解,感兴趣的读者可以参考以获取深入知识(Nithianandarajah-Jones等人,2012年;Monti等人,《癌症》(巴塞尔),2022年,14卷)。本综述的主要目的是强调ERK5的基本特征,并阐明其激活的复杂性质,特别关注其在疾病途径中的非催化依赖性功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f2b/10436230/45a6d99dd0a1/fcell-11-1235217-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f2b/10436230/11d0cd73f0d1/fcell-11-1235217-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f2b/10436230/45a6d99dd0a1/fcell-11-1235217-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f2b/10436230/11d0cd73f0d1/fcell-11-1235217-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f2b/10436230/45a6d99dd0a1/fcell-11-1235217-g002.jpg

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Circ Res. 2023 Jun 23;133(1):25-44. doi: 10.1161/CIRCRESAHA.122.322017. Epub 2023 Jun 2.
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Acute pharmacological degradation of ERK5 does not inhibit cellular immune response or proliferation.
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Cell Chem Biol. 2022 Nov 17;29(11):1630-1638.e7. doi: 10.1016/j.chembiol.2022.09.004. Epub 2022 Oct 10.
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Cell Mol Life Sci. 2022 Sep 19;79(10):524. doi: 10.1007/s00018-022-04541-6.
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ERK5 Is a Major Determinant of Chemical Sarcomagenesis: Implications in Human Pathology.ERK5是化学性肉瘤发生的主要决定因素:对人类病理学的启示。
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