Vlodavsky Israel, Elkin Michael, Abboud-Jarrous Ghada, Levi-Adam Flonia, Fuks Liat, Shafat Itay, Ilan Neta
Cancer and Vascular Biology Research Center, Bruce Rappaport Faculty of Medicine, Technion, Haifa, Israel.
Connect Tissue Res. 2008;49(3):207-10. doi: 10.1080/03008200802143281.
Mammalian heparanase, an endoglycosidase-degrading heparan sulfate, is synthesized as a latent 65 kDa precursor that undergoes proteolytic processing, primarily by cathepsin-L, yielding 8 kDa and 50 kDa subunits that heterodimerize to form a highly active enzyme. Enhanced heparanase expression in human tumors correlates with metastatic potential, tumor vascularity, and reduced postoperative survival of cancer patients, attributed to enzymatic and nonenzymatic activities of the heparanase protein. Urinary and plasma levels of heparanase are elevated in cancer patients and suppressed in response to effective anticancer treatments. These observations and the anticancerous effect of heparanase gene silencing and of heparanase-inhibiting molecules suggest that the enzyme is a promising target for anticancer drug development.
哺乳动物乙酰肝素酶是一种降解硫酸乙酰肝素的内切糖苷酶,最初以65 kDa的潜在前体形式合成,该前体主要通过组织蛋白酶L进行蛋白水解加工,产生8 kDa和50 kDa的亚基,这两个亚基异源二聚化形成一种高活性酶。人类肿瘤中乙酰肝素酶表达增强与转移潜能、肿瘤血管生成以及癌症患者术后生存率降低相关,这归因于乙酰肝素酶蛋白的酶活性和非酶活性。癌症患者尿液和血浆中乙酰肝素酶水平升高,而有效的抗癌治疗可使其降低。这些观察结果以及乙酰肝素酶基因沉默和乙酰肝素酶抑制分子的抗癌作用表明,该酶是抗癌药物开发的一个有前景的靶点。