基质金属蛋白酶
血管生成
细胞外基质
炎症
化学
转移
药物输送
金属蛋白酶
伤口愈合
基质金属蛋白酶抑制剂
癌症研究
细胞生物学
金属蛋白酶组织抑制剂
癌症
免疫学
生物化学
生物
医学
内科学
有机化学
作者
Chenyun Zhang,Gan Jiang,Xiaoling Gao
标识
DOI:10.1021/acs.bioconjchem.3c00266
摘要
Matrix metalloproteinases (MMPs) are a class of endopeptidases that are dependent on zinc and facilitate the degradation of extracellular matrix (ECM) proteins, thereby playing pivotal parts in human physiology and pathology. MMPs regulate normal tissue and cellular functions, including tissue development, remodeling, angiogenesis, bone formation, and wound healing. Several diseases, including cancer, inflammation, cardiovascular diseases, and nervous system disorders, have been linked to dysregulated expression of specific MMP subtypes, which can promote tumor progression, metastasis, and inflammation. Various MMP-responsive drug delivery and release systems have been developed by harnessing cleavage activities and overexpression of MMPs in affected regions. Herein, we review the structure, substrates, and physiological and pathological functions of various MMPs and highlight the strategies for designing MMP-responsive nanoparticles to improve the targeting efficiency, penetration, and protection of therapeutic payloads.
科研通智能强力驱动
Strongly Powered by AbleSci AI