Center for Molecular Innovation , The Feinstein Institute for Medical Research , 350 Community Drive , Manhasset , New York 11030 , United States.
J Med Chem. 2018 Jun 28;61(12):5093-5107. doi: 10.1021/acs.jmedchem.7b01136. Epub 2018 Jan 5.
High mobility group box-1 (HMGb1) protein, a nuclear non-histone protein that is released or secreted from the cell in response to damage or stress, is a sentinel for the immune system that plays a critical role in cell survival/death pathways. This review highlights key features of the endogenous danger-associated molecular pattern (DAMP) protein, HMGb1 in the innate inflammatory response along with various cofactors and receptors that regulate its downstream effects. The evidence demonstrating increased levels of HMGb1 in human inflammatory diseases and conditions is presented, along with a summary of current small molecule or peptide-like antagonists proven to specifically target HMGb1. Additionally, we delineate the measures needed toward validating this protein as a clinically relevant biomarker or bioindicator and as a relevant drug target.
高迁移率族蛋白 B1(HMGb1)是一种核非组蛋白蛋白,在受到损伤或应激时从细胞中释放或分泌出来,它是免疫系统的“哨兵”,在细胞存活/死亡途径中起着关键作用。本综述强调了固有炎症反应中内源性危险相关分子模式(DAMP)蛋白 HMGb1 的关键特征,以及调节其下游效应的各种辅助因子和受体。本文介绍了在人类炎症性疾病和病症中 HMGb1 水平升高的证据,并总结了目前已被证明可特异性靶向 HMGb1 的小分子或肽样拮抗剂。此外,我们还阐述了将该蛋白作为临床相关生物标志物或生物指标以及相关药物靶点进行验证所需的措施。