Department of Breast Surgery, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Int J Biol Markers. 2013 Jun 28;28(2):117-30. doi: 10.5301/jbm.5000026.
Matrix metalloproteinases (MMPs) are endopeptidases that are involved in extracellular matrix degradation. They are also implicated in a number of abnormal bioprocesses, such as tumor growth, invasion, and metastasis. Therefore, controlling MMP activities has generated considerable interest as a possible therapeutic target. The tissue inhibitors of metalloproteinases (TIMPs) are the major naturally occurring proteins that specifically inhibit MMPs and assist in maintaining the balance between extracellular matrix destruction and formation. However, TIMPs are probably not suitable for pharmacological applications due to their short half-lives in vivo. During the last few decades, synthetic MMP inhibitors (MMPIs) have undergone rapid clinical development in attempts to control MMP enzymatic activities in abnormal bioprocesses. Although studies with these agents have met with limited clinical success, the field of MMPIs is still expanding, and generation of highly effective and selective MMPIs might be a promising direction of this research area.
基质金属蛋白酶(MMPs)是参与细胞外基质降解的内肽酶。它们还与许多异常的生物过程有关,如肿瘤生长、侵袭和转移。因此,控制 MMP 的活性作为一种可能的治疗靶点引起了相当大的兴趣。基质金属蛋白酶抑制剂(TIMPs)是主要的天然存在的蛋白质,特异性抑制 MMPs,并有助于维持细胞外基质破坏和形成之间的平衡。然而,由于 TIMPs 在体内的半衰期较短,它们可能不适合用于药理学应用。在过去的几十年中,合成基质金属蛋白酶抑制剂(MMPIs)在尝试控制异常生物过程中的 MMP 酶活性方面经历了快速的临床发展。尽管这些药物的研究取得了有限的临床成功,但 MMPIs 领域仍在不断发展,生成高效和选择性的 MMPIs 可能是该研究领域的一个有前途的方向。