Nm23-H1 的激活通过氧化还原调控抑制乳腺癌转移。

Activation of Nm23-H1 to suppress breast cancer metastasis via redox regulation.

机构信息

College of Pharmacy and Graduate School of Pharmaceutical Sciences, Ewha Womans University, Seoul, South Korea.

出版信息

Exp Mol Med. 2021 Mar;53(3):346-357. doi: 10.1038/s12276-021-00575-1. Epub 2021 Mar 22.

Abstract

Non-metastatic protein 23 H1 (Nm23-H1), a housekeeping enzyme, is a nucleoside diphosphate kinase-A (NDPK-A). It was the first identified metastasis suppressor protein. Nm23-H1 prolongs disease-free survival and is associated with a good prognosis in breast cancer patients. However, the molecular mechanisms underlying the role of Nm23-H1 in biological processes are still not well understood. This is a review of recent studies focusing on controlling NDPK activity based on the redox regulation of Nm23-H1, structural, and functional changes associated with the oxidation of cysteine residues, and the relationship between NDPK activity and cancer metastasis. Further understanding of the redox regulation of the NDPK function will likely provide a new perspective for developing new strategies for the activation of NDPK-A in suppressing cancer metastasis.

摘要

非转移性蛋白 23 H1(Nm23-H1),一种管家酶,是核苷二磷酸激酶-A(NDPK-A)。它是第一个被鉴定出的转移抑制蛋白。Nm23-H1 延长无病生存期,并与乳腺癌患者的良好预后相关。然而,Nm23-H1 在生物过程中发挥作用的分子机制仍不清楚。这是一篇综述,重点介绍了基于 Nm23-H1 的氧化还原调控、与半胱氨酸残基氧化相关的结构和功能变化以及 NDPK 活性与癌症转移之间的关系,来控制 NDPK 活性的最新研究。进一步了解 NDPK 功能的氧化还原调控可能为开发新的策略提供新的视角,以激活 NDPK-A 抑制癌症转移。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0eb/8080780/bec6b85b9cf3/12276_2021_575_Fig1_HTML.jpg

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