Actions of derivatives of dehydroaltenusin, a new mammalian DNA polymerase α-specific inhibitor

被引:17
作者
Kamisuki, S
Murakami, C
Ohta, K
Yoshida, H
Sugawara, F
Sakaguchi, K
Mizushina, Y [1 ]
机构
[1] Kobe Gakuin Univ, Dept Nutr Sci, Lab Food & Nutr Sci, Nishi Ku, Kobe, Hyogo 6512180, Japan
[2] Sci Univ Tokyo, Fac Sci & Technol, Dept Appl Biol Sci, Noda, Chiba 2788510, Japan
[3] Kobe Gakuin Univ, High Technol Res Ctr, Nishi Ku, Kobe, Hyogo 6512180, Japan
关键词
DNA polymerase alpha; dehydroaltenusin; enzyme inhibitor; DNA replication; cytotoxicity; cell proliferation; apoptosis;
D O I
10.1016/S0006-2952(01)00912-1
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Dehydroaltenusin was found to be an inhibitor of mammalian DNA polymerase alpha (pot. alpha) in vitro, but did not influence the activities of the other replicative DNA polymerases including even other vertebrate pot. alpha. In this study, we purified or synthesized various slightly modified derivatives of dehydroaltenusin, and using them, investigated the relationship between the chemical structure and the inhibitory effects, and the in vitro and in vivo effects of dehydroaltenusin to determine to what extent the pol. alpha activity inhibition influences cell proliferation. Most of the derivatives lost the enzyme species-specific inhibitory effect, suggesting that dehydroaltenusin is three-dimensionally inserted into a pocket present only in mammalian pot. alpha. Dehydroaltenusin inhibited the cell proliferation of the human gastric cancer cell line NUGC-3 by arresting the cells at G1/S-phase, and prevented the incorporation of thymidine into the cells, indicating that it blocks the primary step of in vivo DNA replication by inhibiting pot. alpha. This compound also induced apoptosis of the cells. Dehydroaltenusin is a mammalian pot. alpha-specific inhibitor useful in both of in vivo and in vitro experiments. (C) 2002 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:421 / 427
页数:7
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