@article{oai:repo.qst.go.jp:00043040,
 author = {Takahashi, Sentaro and Sato, Hiroshi and Kubota, Yoshihisa and S., Bedford Joel and Okayasu, Ryuichi and 高橋 千太郎 and 佐藤 宏 and 久保田 善久 and 岡安 隆一},
 journal = {Toxicology},
 month = {},
 note = {DNA double strand breaks (DSBs), induced by gamma-irradiation in Chinese hamster ovary cells, were used to examine whether antimony compounds affect the repair of DNA damage. The cells were first incubated with antimony trichloride or antimony potassium tartrate (both Sb(III)) for 2 h, and then irradiated with gamma-rays at a dose of 40 Gy. The DNA DSB was quantified with pulsed field gel electrophoresis immediately after irradiation (non-repair group) as well as at 30 min post-irradiation (repair group). The degree of repair inhibition was determined by the differences in the amount of DNA DSB between non-repair and repair groups. Both antimony compounds inhibited repair of DNA DSB in a dose dependent manner. In trichloride, 0.2 mM antimony significantly inhibited the rejoining of DSB, while 0.4 mM was necessary in potassium antimony tartrate. The mean lethal doses, D0, for the treatment with antimony trichloride and antimony potassium tartrate, were approximately 0.21 and 0.12 mM, respectively. This indicates that the repair inhibition by antimony trichloride occurred in the dose range near D0, but the antimony potassium tartrate inhibited the repair at doses where most cells lost their proliferating ability. This is the first report to indicate that antimony compounds may inhibit the repair of radiation-induced DNA DSB.},
 pages = {249--256},
 title = {Inhibition of DNA-double strand break repair by antimony compounds},
 volume = {180},
 year = {2002}
}