Isodiospyrin as a novel human DNA topoisomerase I inhibitor

  • Biochem Pharmacol. 2003 Nov 15;66(10):1981-91. doi: 10.1016/j.bcp.2003.07.003.
Chun-Yuan Ting  1 ,  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
Affiliations
  • 1. Institute of Biochemistry, School of Life Science, National Yang Ming University, Taipei, Taiwan.
Abstract

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.

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