Isodiospyrin as a novel human DNA topoisomerase I inhibitor

Chun Yuan Ting, Chia Tse Hsu, Hsiang Ting Hsu, Jin Shan Su, Tzong Yueh Chen, Woan Yuh Tarn, Yao Haur Kuo, Jacqueline Whang-Peng, Leroy F. Liu, Jaulang Hwang

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52 引文 斯高帕斯(Scopus)

摘要

Isodiospyrin is a natural product from the plant Diospyros morrisiana, which consists of an asymmetrical 1,2-binaphthoquinone chromophore. Isodiospyrin exhibits cytotoxic activity to tumor cell lines but very little is known about its cellular target and mechanism of action. Unlike the prototypic human topoisomerase I (htopo I) poison camptothecin, isodiospyrin does not induce htopo I-DNA covalent complexes. However, isodiospyrin antagonizes camptothecin-induced, htopo I-mediated DNA cleavage. Binding analysis indicated that isodiospyrin binds htopo I but not DNA. These results suggest that isodiospyrin inhibits htopo I by direct binding to htopo I, which limits htopo I access to the DNA substrate. Furthermore, isodiospyrin exhibits strong inhibitory effect on the kinase activity of htopo I toward splicing factor 2/alternate splicing factor in the absence of DNA. Thus, these findings have important implications on naphthoquinone and its derivatives' cellular mode of actions, i.e. these novel DNA topoisomerase I inhibitors can prevent both DNA relaxation and kinase activities of htopo I.
原文英語
頁(從 - 到)1981-1991
頁數11
期刊Biochemical Pharmacology
66
發行號10
DOIs
出版狀態已發佈 - 十一月 15 2003
對外發佈Yes

ASJC Scopus subject areas

  • Pharmacology

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