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高迁移率族蛋白B1(HMGB1):细胞内外的治疗靶点

HMGB1 Protein: A Therapeutic Target Inside and Outside the Cell.

作者信息

Ugrinova I, Pasheva E

机构信息

"Roumen Tsanev" Institute of Molecular Biology, Bulgarian Academy of Sciences, Sofia, Bulgaria.

"Roumen Tsanev" Institute of Molecular Biology, Bulgarian Academy of Sciences, Sofia, Bulgaria.

出版信息

Adv Protein Chem Struct Biol. 2017;107:37-76. doi: 10.1016/bs.apcsb.2016.10.001. Epub 2016 Dec 2.

DOI:10.1016/bs.apcsb.2016.10.001
PMID:28215228
Abstract

High-mobility group box 1 protein (HMGB1) is a nonhistone chromosomal protein discovered more than 30 years ago. It is an abundant nuclear protein that has a dual function-in the nucleus, it binds DNA and participates in practically all DNA-dependent processes serving as an architectural factor. Outside the cell, HMGB1 plays a different role-it acts as an alarmine that activates a large number of HMGB1-"competent" cells and mediates a broad range of physiological and pathological responses. This universality makes it an attractive target for innovative therapeutic strategies in the treatment of various diseases. Here we present an overview of the major nuclear and extracellular properties of HMGB1 and describe its interaction with different molecular partners as specific receptors or inhibitors, which are important for its role as a target in multiple diseases. We highlight its pivotal role as a target for cancer treatment at two aspects: first in terms of its substantial impact on the repair capacity of cancer cells, thus affecting the effectiveness of chemotherapy with the antitumor drug cis-platinum and, second, the possibility to be targeted by microRNAs influencing different pathways of human diseases, thus making it a promising candidate for a new strategy for therapeutic interventions against various pathological conditions but mainly cancer.

摘要

高迁移率族蛋白B1(HMGB1)是30多年前发现的一种非组蛋白染色体蛋白。它是一种丰富的核蛋白,具有双重功能——在细胞核内,它结合DNA并参与几乎所有依赖DNA的过程,作为一种结构因子发挥作用。在细胞外,HMGB1发挥着不同的作用——它作为一种警报素,激活大量对HMGB1“敏感”的细胞,并介导广泛的生理和病理反应。这种通用性使其成为治疗各种疾病的创新治疗策略的一个有吸引力的靶点。在此,我们概述了HMGB1的主要核内和细胞外特性,并描述了它与不同分子伴侣(作为特异性受体或抑制剂)的相互作用,这些相互作用对于其在多种疾病中作为靶点的作用很重要。我们从两个方面强调了它作为癌症治疗靶点的关键作用:第一,就其对癌细胞修复能力的重大影响而言,从而影响抗癌药物顺铂化疗的效果;第二,它有可能被影响人类疾病不同途径的微小RNA靶向,因此使其成为针对各种病理状况(主要是癌症)的治疗干预新策略的一个有前景的候选靶点。

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