Davidson Ben, Reich Reuven, Risberg Bjørn, Nesland Jahn M
Department of Pathology, University of Oslo, The Norwegian Radium Hospital, Montebello 0310 Oslo, Norway.
Arkh Patol. 2002 May-Jun;64(3):47-53.
Matrix metalloproteinases (MMP) are zinc-dependent proteolytic enzymes capable of breaking down basement membranes and most extracellular matrix (ECM) components. MMP expression and activation are carefully regulated in physiological conditions in order to prevent uncontrolled destruction of body tissues but this regulation is modified or disrupted in pathological processes, including cancer. This review presents regulatory mechanisms designed to control MMP action. These consist of direct activation and inhibition by tissue inhibitors of MMP (TIMP), signal transduction pathways mediated by adhesion molecules such as integrins and EMMPRIN, involved in activation of MMP synthesis and transcriptional control by the ETS family of transcription factors.
基质金属蛋白酶(MMP)是一类锌依赖性蛋白水解酶,能够分解基底膜和大多数细胞外基质(ECM)成分。在生理条件下,MMP的表达和激活受到严格调控,以防止身体组织不受控制的破坏,但在包括癌症在内的病理过程中,这种调控会被改变或破坏。本综述介绍了旨在控制MMP作用的调控机制。这些机制包括MMP组织抑制剂(TIMP)的直接激活和抑制、由整合素和EMMPRIN等黏附分子介导的信号转导途径,这些途径参与MMP合成的激活以及ETS转录因子家族的转录控制。