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Identification of a small-molecule inhibitor of DNA topoisomerase II by proteomic profiling.

作者信息

Kawatani Makoto, Takayama Hiroshi, Muroi Makoto, Kimura Shinya, Maekawa Taira, Osada Hiroyuki

机构信息

Chemical Biology Core Facility, Chemical Biology Department, RIKEN Advanced Science Institute, Saitama 351-0198, Japan.

出版信息

Chem Biol. 2011 Jun 24;18(6):743-51. doi: 10.1016/j.chembiol.2011.03.012.

Abstract

BNS-22, a chemically synthesized derivative of the natural plant product GUT-70, has antiproliferative activity against human cancer cells, the mechanism of which is unknown. Here, we identify a target of BNS-22 by proteomic profiling analysis, which suggests that BNS-22 belongs to the same cluster as ICRF-193, a DNA topoisomerase II (TOP2) catalytic inhibitor. BNS-22 inhibits kinetoplast DNA decatenation that is mediated by human TOP2α and TOP2β in vitro at an IC(50) of 2.8 and 0.42 μM, respectively. BNS-22 does not affect DNA damage and antagonizes TOP2 poison-mediated DNA damage. Like ICRF-193, BNS-22 induces mitotic abnormalities, characterized by impairments in chromosome alignment and segregation, thereby causing polyploidy in HeLa cells. These results indicate that BNS-22 targets TOP2 and acts as its catalytic inhibitor.

摘要

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