Mangold U
Program in Vascular Biology, Children's Hospital, Karp Family Building, 1 Blackfan Circle, Boston, Massachusetts 02115, USA.
Cell Mol Life Sci. 2006 Sep;63(18):2095-101. doi: 10.1007/s00018-005-5583-4.
In contrast to the considerable interest in the oncogene ornithine decarboxylase (ODC) and in the family of antizymes with regard to cell proliferation and tumorigenesis, the endogenous antizyme inhibitor (AZI) has been less well studied. AZI is highly homologous to the enzyme ODC but does not possess any decarboxylase activity. Elevated ODC activity is associated with most forms of human malignancies. Antizymes bind ODC, inhibit ODC activity and promote the ubiquitin-independent degradation of ODC. Consequently they are proposed as tumor suppressors. In particular, the most studied member of the antizyme family, antizyme 1, has been demonstrated to play a role in tumor suppression. AZI inactivates all members of the antizyme family, reactivates ODC and prevents the proteolytic degradation of ODC, which may suggest a role for AZI in tumor progression.
与人们对癌基因鸟氨酸脱羧酶(ODC)以及抗酶家族在细胞增殖和肿瘤发生方面的浓厚兴趣形成对比的是,内源性抗酶抑制剂(AZI)的研究较少。AZI与酶ODC高度同源,但不具备任何脱羧酶活性。ODC活性升高与大多数人类恶性肿瘤形式相关。抗酶结合ODC,抑制ODC活性并促进ODC不依赖泛素的降解。因此,它们被认为是肿瘤抑制因子。特别是,抗酶家族中研究最多的成员抗酶1已被证明在肿瘤抑制中发挥作用。AZI使抗酶家族的所有成员失活,重新激活ODC并防止ODC的蛋白水解降解,这可能表明AZI在肿瘤进展中起作用。