Matrix metalloproteinase 9 (MMP9) in wound healing of diabetic foot ulcer: Molecular target and structure-based drug design

Q1 Medicine
Maywan Hariono, Sri H. Yuliani, Enade P. Istyastono, Florentinus D.O. Riswanto, Christophorus F. Adhipandito
{"title":"Matrix metalloproteinase 9 (MMP9) in wound healing of diabetic foot ulcer: Molecular target and structure-based drug design","authors":"Maywan Hariono,&nbsp;Sri H. Yuliani,&nbsp;Enade P. Istyastono,&nbsp;Florentinus D.O. Riswanto,&nbsp;Christophorus F. Adhipandito","doi":"10.1016/j.wndm.2018.05.003","DOIUrl":null,"url":null,"abstract":"<div><p>Matrix Metalloproteinase 9 (MMP9) is one of the many zinc-dependent endopeptidases found in the body, which is also involved in delaying wound healing by degrading extracellular matrices associated with normal tissue remodelling processes. In Diabetic Foot Ulcer (DFU), this protein is highly expressed especially at the stage where wound healing is poor. Currently, MMP9 is becoming one of the interesting targets in the discovery and development of MMP inhibitors, mainly in cancer treatment. There are at least 18 MMP9 crystal structures that are available in protein data bank (PDB) which can be utilised for structure based drug design. This review will discuss the role of MMP9 in wound healing associated with DFU at molecular level, followed by the recent progress of MMP9 inhibitors that have been identified in the last two decades.</p></div>","PeriodicalId":38278,"journal":{"name":"Wound Medicine","volume":"22 ","pages":"Pages 1-13"},"PeriodicalIF":0.0000,"publicationDate":"2018-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.wndm.2018.05.003","citationCount":"29","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Wound Medicine","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2213909517300721","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 29

Abstract

Matrix Metalloproteinase 9 (MMP9) is one of the many zinc-dependent endopeptidases found in the body, which is also involved in delaying wound healing by degrading extracellular matrices associated with normal tissue remodelling processes. In Diabetic Foot Ulcer (DFU), this protein is highly expressed especially at the stage where wound healing is poor. Currently, MMP9 is becoming one of the interesting targets in the discovery and development of MMP inhibitors, mainly in cancer treatment. There are at least 18 MMP9 crystal structures that are available in protein data bank (PDB) which can be utilised for structure based drug design. This review will discuss the role of MMP9 in wound healing associated with DFU at molecular level, followed by the recent progress of MMP9 inhibitors that have been identified in the last two decades.

Abstract Image

基质金属蛋白酶9 (MMP9)在糖尿病足溃疡创面愈合中的作用:分子靶点和基于结构的药物设计
基质金属蛋白酶9 (Matrix Metalloproteinase 9, MMP9)是体内发现的众多锌依赖性内肽酶之一,它也参与通过降解与正常组织重塑过程相关的细胞外基质来延缓伤口愈合。在糖尿病足溃疡(DFU)中,这种蛋白高度表达,特别是在伤口愈合不良的阶段。目前,MMP9正成为MMP抑制剂发现和开发的有趣靶点之一,主要用于癌症治疗。蛋白质数据库(PDB)中至少有18个MMP9晶体结构可用于基于结构的药物设计。本文将在分子水平上讨论MMP9在DFU相关伤口愈合中的作用,以及在过去二十年中发现的MMP9抑制剂的最新进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Wound Medicine
Wound Medicine Medicine-Surgery
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信