Kadmon D
Scott Department of Urology, Baylor College of Medicine, Houston, Texas 77030.
J Cell Biochem Suppl. 1992;16H:122-7. doi: 10.1002/jcb.240501228.
The polyamines are normal cell constituents considered to have an important role in the regulation of proliferation and differentiation. DFMO is an irreversible, enzyme-activated, suicide inhibitor of ornithine decarboxylase (ODC), the enzyme responsible for the first and rate-limiting step in mammalian polyamine synthesis. Preliminary data show that DFMO inhibits tumor cell growth in vitro and in vivo, and that it demonstrates chemopreventive activity in a variety of animal tumors. The prostate contains some of the highest concentrations of polyamines and of polyamine-synthetic enzymes (including ODC) in the mammalian organism. ODC activity in the prostate was shown to be more susceptible to DFMO inhibition than in other organs. We have found the ODC activity of the Dunning R3327 rat prostatic carcinomas to be as sensitive to inhibition by DFMO as the normal rat prostate. Furthermore, DFMO was inhibitory to the growth of the tumor both in vitro and in vivo. Given the slow growth rate and long latency period of human prostate cancer and the preliminary DFMO data, we suggest that clinical trials to evaluate the chemopreventive potential of DFMO in prostatic carcinoma deserve serious consideration.
多胺是正常细胞成分,被认为在细胞增殖和分化的调节中起重要作用。二氟甲基鸟氨酸(DFMO)是鸟氨酸脱羧酶(ODC)的一种不可逆的、酶激活的自杀性抑制剂,ODC是哺乳动物多胺合成的第一步及限速步骤所涉及的酶。初步数据表明,DFMO在体外和体内均能抑制肿瘤细胞生长,并且在多种动物肿瘤中显示出化学预防活性。在哺乳动物机体中,前列腺含有一些浓度最高的多胺和多胺合成酶(包括ODC)。结果显示,前列腺中的ODC活性比其他器官更容易受到DFMO抑制。我们发现,邓宁R3327大鼠前列腺癌的ODC活性对DFMO抑制的敏感性与正常大鼠前列腺一样。此外,DFMO在体外和体内均能抑制肿瘤生长。鉴于人类前列腺癌生长缓慢、潜伏期长以及DFMO的初步数据,我们认为,评估DFMO在前列腺癌中化学预防潜力的临床试验值得认真考虑。