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新型DNA聚合酶抑制剂组——合成磺基喹喔啉基酰基甘油的研究:对细胞增殖的抑制作用

Studies on a novel DNA polymerase inhibitor group, synthetic sulfoquinovosylacylglycerols: inhibitory action on cell proliferation.

作者信息

Ohta K, Hanashima S, Mizushina Y, Yamazaki T, Saneyoshi M, Sugawara F, Sakaguchi K

机构信息

Department of Applied Biological Science, Faculty of Science and Technology, Science University of Tokyo, Chiba-ken 278-8510, Noda, Japan.

出版信息

Mutat Res. 2000 May 8;467(2):139-52. doi: 10.1016/s1383-5718(00)00028-0.

DOI:10.1016/s1383-5718(00)00028-0
PMID:10838201
Abstract

Some chemically synthesized sulfoquinovosylmonoacylglycerols (SQMG)-sulfoquinovosyldiacylglycerols (SQDG) have been reported to selectively and strongly inhibit the activities of mammalian DNA polymerases alpha and beta in vitro. In this study, using human cancer cell lines, we investigated the effects of SQMG-SQDG on the DNA polymerase in the cells. In the presence of n-decane, the IC(50) values on cell growth were approximately 1-5 microM for SQMG and about 0.3-1 microM for SQDG. The values were almost the same as the in vitro enzyme inhibitory levels. The cell lines were arrested in early S-phase by SQMG-SQDG at the concentrations of 0.1-4.7 microM in a manner dependent on incubation time, suggesting that SQMG-SQDG blocked the primary step of DNA replication by inhibiting DNA polymerase, possibly alpha-type. We also demonstrated the localization of SQMG in the cell using the fluorescent SQMG analog, SQMGalpha-NBDD, which was synthesized in our laboratory. SQMGalpha-NBDD was localized in the nucleus and on the nuclear surface, but the binding site seemed not to be the DNA/chromatin, suggesting that the SQMG-SQDG might interact with molecules located close to the DNA/chromatin and on the nuclear surface. These results suggested a correlation between the in vitro biochemical action of the SQMG-SQDGs and their intracellular mode of action.

摘要

据报道,一些化学合成的磺基喹喔啉单酰甘油(SQMG)-磺基喹喔啉二酰甘油(SQDG)在体外能选择性且强烈地抑制哺乳动物DNA聚合酶α和β的活性。在本研究中,我们使用人类癌细胞系,研究了SQMG-SQDG对细胞中DNA聚合酶的影响。在正癸烷存在的情况下,SQMG对细胞生长的IC(50)值约为1-5微摩尔,SQDG约为0.3-1微摩尔。这些值与体外酶抑制水平几乎相同。在0.1-4.7微摩尔浓度下,SQMG-SQDG能以依赖孵育时间的方式使细胞系停滞在S期早期,这表明SQMG-SQDG通过抑制DNA聚合酶(可能是α型)阻断了DNA复制的第一步。我们还使用在我们实验室合成的荧光SQMG类似物SQMGα-NBDD证明了SQMG在细胞中的定位。SQMGα-NBDD定位于细胞核和核表面,但结合位点似乎不是DNA/染色质,这表明SQMG-SQDG可能与位于DNA/染色质附近和核表面的分子相互作用。这些结果表明SQMG-SQDG的体外生化作用与其细胞内作用模式之间存在相关性。

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