Himelstein B P, Canete-Soler R, Bernhard E J, Dilks D W, Muschel R J
Division of Oncology, Children's Hospital of Philadelphia, PA 19104, USA.
Invasion Metastasis. 1994;14(1-6):246-58.
Many enzymes capable of proteolytic degradation of extracellular matrix and basement membranes have been implicated in tumor progression, including the matrix metalloproteinases, cathepsins, plasminogen activators, and heparanase. Matrix metalloproteinases, a family of zinc-dependent proteases, participate in several steps in tumor progression, including invasion, metastasis, and angiogenesis. In this review, we will give a brief overview of this protease family, and we will review in vitro and in vivo evidence implicating a particular metalloproteinase, the 92-kD type IV collagenase/gelatinase (MMP-9 or gelatinase B), as well as other metalloproteinases, in cancer progression. Finally, using recent studies from our laboratory, we will demonstrate the importance of both tumor cell and host stromal cell production of MMP-9 in tumor progression.
许多能够蛋白水解降解细胞外基质和基底膜的酶与肿瘤进展有关,包括基质金属蛋白酶、组织蛋白酶、纤溶酶原激活剂和乙酰肝素酶。基质金属蛋白酶是一类锌依赖性蛋白酶,参与肿瘤进展的多个步骤,包括侵袭、转移和血管生成。在本综述中,我们将简要概述这个蛋白酶家族,并回顾体外和体内证据,这些证据表明一种特定的金属蛋白酶,即92-kD IV型胶原酶/明胶酶(MMP-9或明胶酶B)以及其他金属蛋白酶与癌症进展有关。最后,利用我们实验室最近的研究,我们将证明肿瘤细胞和宿主基质细胞产生MMP-9在肿瘤进展中的重要性。