Shigesawa A, Onoda N, Chung Y S, Yano Y, Otani S, Fukushima S, Sowa M
First Department of Surgery, Osaka City University Medical School, Osaka 545, Japan.
Oncol Rep. 1998 Jan-Feb;5(1):125-9. doi: 10.3892/or.5.1.125.
Spermidine/spermine N1-acetyltransferase (SSAT), rate-limiting enzyme of polyamine interconversion, has been demonstrated to play an important role in malignant transformation of cells. We examined the involvement of altered polyamine metabolism in the colonic carcinogenesis, using 1,2-dimethylhydrazine (DMH)-induced rat colon tumor model. Following findings were obtained: i) Ornithine decarboxylase demonstrated high activity from the early phase in colon mucosa, and increased significantly in tumors. ii) Spermidine and spermine levels gradually elevated in DMH-treated mucosa, while putrescine increased significantly in tumor tissues. iii) SSAT activity increased gradually in DMH-treated colon mucosa, which preceded elevation of tissue putrescine level, and coincided with tumor development. In conclusion, elevation of putrescine level and induction of SSAT activity are suggested to have a close association in colonic carcinogenesis.
亚精胺/精胺N1 - 乙酰基转移酶(SSAT)是多胺相互转化的限速酶,已被证明在细胞恶性转化中起重要作用。我们使用1,2 - 二甲基肼(DMH)诱导的大鼠结肠癌模型,研究了多胺代谢改变在结肠癌发生中的作用。获得了以下结果:i)鸟氨酸脱羧酶在结肠黏膜早期就表现出高活性,在肿瘤中显著增加。ii)在DMH处理的黏膜中,亚精胺和精胺水平逐渐升高,而腐胺在肿瘤组织中显著增加。iii)在DMH处理的结肠黏膜中,SSAT活性逐渐增加,这先于组织腐胺水平的升高,并与肿瘤发展一致。总之,腐胺水平的升高和SSAT活性的诱导在结肠癌发生中可能密切相关。