1. Academic Validation
  2. Identification of a small-molecule inhibitor of DNA topoisomerase II by proteomic profiling

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

  • Chem Biol. 2011 Jun 24;18(6):743-51. doi: 10.1016/j.chembiol.2011.03.012.
Makoto Kawatani 1 Hiroshi Takayama Makoto Muroi Shinya Kimura Taira Maekawa Hiroyuki Osada
Affiliations

Affiliation

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

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