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Early inhibition of DNA synthesis in the developing rat cerebral cortex by the purine analogues olomoucine and roscovitine.

作者信息

Yakisich J S, Sidén A, Idoyaga Vargas V, Eneroth P, Cruz M

机构信息

Clinical Research Center, Karolinska Institute, Novum, Sweden.

出版信息

Biochem Biophys Res Commun. 1998 Feb 24;243(3):674-7. doi: 10.1006/bbrc.1998.8157.

DOI:10.1006/bbrc.1998.8157
PMID:9500988
Abstract

The effects of the cyclin-dependent kinase (CDK) inhibitors olomoucine and roscovitine on DNA synthesis were studied using short time incubation (30-90 minutes). Both purine analogues at concentrations from 1-100 microM decreased the DNA synthesis of rat brain cortex in a dose-dependent manner and the maximum effect occurred within 30 min of incubation. Staurosporine, another potent CDK inhibitor did not affect the DNA synthesis in the concentration range 1-250 nM. These results indicate that olomoucine and roscovitine block DNA synthesis by a mechanism independent of CDK inhibition. We propose that the cellular effects of olomuocine and roscovitine on the cell cycle are at least in part due to this early inhibitory effect on DNA synthesis.

摘要

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1
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引用本文的文献

1
Strong inhibition of replicative DNA synthesis in the developing rat cerebral cortex and glioma cells by roscovitine.罗克洛文强烈抑制发育中的大鼠大脑皮层和神经胶质瘤细胞的复制性 DNA 合成。
Invest New Drugs. 2010 Jun;28(3):299-305. doi: 10.1007/s10637-009-9254-4. Epub 2009 Apr 24.