Suppr超能文献

血管生成中的基质金属蛋白酶和基质因子

Matrix metalloproteinases and matrikines in angiogenesis.

作者信息

Bellon Georges, Martiny Laurent, Robinet Arnaud

机构信息

FRE 2534 CNRS, Faculty of Medicine, IFR-53 "Biomolécules", University of Reims Champagne-Ardenne, 51 rue Cognacq Jay, 51095 Reims Cedex, France.

出版信息

Crit Rev Oncol Hematol. 2004 Mar;49(3):203-20. doi: 10.1016/j.critrevonc.2003.10.004.

Abstract

Neoangiogenesis, the formation of new blood capillaries from pre-existing vessels, plays an important role in a number of physiological and pathological processes, particularly in tumor growth and metastasis. Extracellular proteolysis by matrix metalloproteinases or other neutral proteinases is an absolute requirement for initiating tumor invasion and angiogenesis. Cryptic segments or pre-existing domains within larger proteins, most of them belonging to the extracellular matrix, can be exposed by conformational changes and/or generated by partial enzymatic hydrolysis. They can positively or negatively regulate important functions of endothelial cells including adhesion, migration, proliferation, cell survival and cell-cell interactions. Such regulations by cryptic segments and proteolytic fragments led to the concept of matricryptins and matrikines, respectively. Matrix metalloproteinases and matrikines in conjunction with other pro- or anti-angiogenic factors might act in concert at any step of the angiogenesis process. A number of matrikines have been identified as potent anti-angiogenic factors, which could provide a new alternative to anti-proteolytic strategies for the development of anti-angiogenic therapeutic molecules aimed at inhibiting tumor growth and metastasis. Some of them are currently being investigated in clinical trials.

摘要

新生血管生成,即从已有的血管形成新的毛细血管,在许多生理和病理过程中发挥着重要作用,尤其是在肿瘤生长和转移过程中。基质金属蛋白酶或其他中性蛋白酶介导的细胞外蛋白水解是启动肿瘤侵袭和血管生成的绝对必要条件。较大蛋白质中的隐蔽片段或已有的结构域,其中大多数属于细胞外基质,可通过构象变化暴露和/或通过部分酶促水解产生。它们可以正向或负向调节内皮细胞的重要功能,包括黏附、迁移、增殖、细胞存活和细胞间相互作用。这种由隐蔽片段和蛋白水解片段进行的调节分别导致了基质隐窝蛋白和基质因子的概念。基质金属蛋白酶和基质因子与其他促血管生成或抗血管生成因子可能在血管生成过程的任何步骤协同作用。许多基质因子已被确定为有效的抗血管生成因子,这可能为旨在抑制肿瘤生长和转移的抗血管生成治疗分子的开发提供一种替代抗蛋白水解策略的新方法。其中一些目前正在临床试验中进行研究。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验