Weber G
Clin Biochem. 1983 Feb;16(1):57-63. doi: 10.1016/s0009-9120(83)94432-6.
In cancer cells, a marked imbalance in the enzymic pattern of purine metabolism is linked with transformation and/or progression. In chemically-induced, transplantable hepatomas in rat, the specific activities of the anabolic enzymes, IMP dehydrogenase, GMP synthetase, adenylosuccinate synthetase, adenylosuccinase, AMP deaminase and amidophosphoribosyltransferase, increased to 13.5-, 3.7-, 3.1-, 1.8-, 5.5- and 2.8-fold, respectively, of those in normal liver. Activities of the catabolic enzymes, inosine phosphorylase, xanthine oxidase and uricase, decreased to 19, 10 and 4%, respectively. This enzymic imbalance was specific to hepatic neoplasia, since no similar pattern was observed in differentiating or regenerating liver. Most enzymic alterations were present also in chemically- and virus-induced animal tumors, in human kidney, liver and colon carcinomas, and in human colon carcinoma xenografts. The molecular correlation concept applies to purine biochemistry and an important segment of neoplastic gene expression was identified in the behavior of key purine-metabolizing enzymes.
在癌细胞中,嘌呤代谢酶模式的显著失衡与细胞转化和/或进展相关。在化学诱导的大鼠可移植肝癌中,合成代谢酶(肌苷酸脱氢酶、鸟苷酸合成酶、腺苷酸琥珀酸合成酶、腺苷酸琥珀酸裂解酶、AMP脱氨酶和氨甲酰磷酸核糖基转移酶)的比活性分别增加至正常肝脏的13.5倍、3.7倍、3.1倍、1.8倍、5.5倍和2.8倍。分解代谢酶(肌苷磷酸化酶、黄嘌呤氧化酶和尿酸酶)的活性分别降至19%、10%和4%。这种酶失衡是肝脏肿瘤所特有的,因为在分化或再生的肝脏中未观察到类似模式。大多数酶改变也存在于化学和病毒诱导的动物肿瘤、人类肾癌、肝癌和结肠癌以及人结肠癌异种移植瘤中。分子相关概念适用于嘌呤生物化学,并且在关键嘌呤代谢酶的行为中确定了肿瘤基因表达的一个重要部分。