Devy Laetitia, Dransfield Daniel T
Merck Serono S.A., 9 Chemin des Mines, Case postale 54, 1211 Geneva 20, Switzerland.
Biochem Res Int. 2011;2011:191670. doi: 10.1155/2011/191670. Epub 2010 Oct 28.
MMP intervention strategies have met with limited clinical success due to severe toxicities. In particular, treatment with broad-spectrum MMP-inhibitors (MMPIs) caused musculoskeletal pain and inflammation. Selectivity may be essential for realizing the clinical potential of MMPIs. Here we review discoveries pinpointing membrane-bound MMPs as mediators of mechanisms underlying cancer and inflammation and as possible therapeutic targets for prevention/treatment of these diseases. We discuss strategies to target these therapeutic proteases using highly selective inhibitory agents (i.e., human blocking antibodies) against individual membrane-bound MMPs.
由于严重的毒性,基质金属蛋白酶(MMP)干预策略在临床上取得的成功有限。特别是,使用广谱MMP抑制剂(MMPIs)进行治疗会引起肌肉骨骼疼痛和炎症。选择性对于实现MMPIs的临床潜力可能至关重要。在这里,我们回顾了一些发现,这些发现确定膜结合MMPs是癌症和炎症潜在机制的介质,也是预防/治疗这些疾病的可能治疗靶点。我们讨论了使用针对单个膜结合MMPs的高度选择性抑制剂(即人源阻断抗体)来靶向这些治疗性蛋白酶的策略。