脱氧胞苷
吉西他滨
体内
抗代谢物
癌症研究
脱氧胞苷激酶
白血病
细胞培养
生物活性
体外
化学
内科学
癌症
生物
医学
生物化学
遗传学
生物技术
作者
Larry W. Hertel,G B Boder,Julian S. Kroin,Sharon M. Rinzel,Gerald A. Poore,Glen C. Todd,Gerald B. Grindey
出处
期刊:PubMed
[National Institutes of Health]
日期:1990-07-15
卷期号:50 (14): 4417-22
被引量:683
摘要
A new pyrimidine antimetabolite, 2',2'-difluorodeoxycytidine, Gemcitabine (LY188011, dFdCyd) has been synthesized and evaluated in experimental tumor models. dFdCyd is a very potent and specific deoxycytidine analogue. The concentration required for 50% inhibition of growth is 1 ng/ml in the CCRF-CEM human leukemia cell culture assay. Concurrent addition of deoxycytidine to the cell culture system provides about a 1000-fold decrease in biological activity. The inhibition of growth of human leukemia cells in culture led to the in vivo evaluation of this compound as a potential oncolytic agent. Maximal activity in vivo was seen with dFdCyd when administered on an every third day schedule. 1-beta-D-Arabinofuranosylcytosine, administered on a daily for 10-day schedule, was directly compared to dFdCyd in this evaluation. dFdCyd demonstrated good to excellent antitumor activity in eight of the eight murine tumor models evaluated. 1-beta-D-Arabinofuranosylcytosine was substantially less active or had no activity in these same tumor models. This in vivo activity against murine solid tumors supports the conclusion that dFdCyd is an excellent candidate for clinical trials in the treatment of cancer.
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