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ATM-dependent hyper-radiosensitivity in mammalian cells irradiated by heavy irons.
https://repo.qst.go.jp/records/45704
https://repo.qst.go.jp/records/45704ae9a91fc-9ae2-4367-b928-d70d339fac18
| Item type | 学術雑誌論文 / Journal Article(1) | |||||
|---|---|---|---|---|---|---|
| 公開日 | 2009-12-28 | |||||
| タイトル | ||||||
| タイトル | ATM-dependent hyper-radiosensitivity in mammalian cells irradiated by heavy irons. | |||||
| 言語 | ||||||
| 言語 | eng | |||||
| 資源タイプ | ||||||
| 資源タイプ識別子 | http://purl.org/coar/resource_type/c_6501 | |||||
| 資源タイプ | journal article | |||||
| アクセス権 | ||||||
| アクセス権 | metadata only access | |||||
| アクセス権URI | http://purl.org/coar/access_right/c_14cb | |||||
| 著者 |
XUE, Lian
× XUE, Lian× Yu, Dong× Furusawa, Yoshiya× Cao, JianPing× Okayasu, Ryuichi× Fan, SaiJun× 薛 蓮× 于 冬× 古澤 佳也× 岡安 隆一 |
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| 抄録 | ||||||
| 内容記述タイプ | Abstract | |||||
| 内容記述 | PURPOSE: Low-dose hyper-radiosensitivity (HRS) and the later appearing radioresistance (termed induced radioresistance [IRR]) was mainly studied in low linear energy transfer (LET) radiation with survival observation. The aim of this study was to find out whether equivalent hypersensitivity occurred in high LET radiation, and the roles of ataxia telangiectasia mutated (ATM) kinase. METHODS AND MATERIALS: Survival and mutation were measured by clonogenic assay and HPRT mutation assay. ATM Ser1981 activation was detected by Western blotting and immunofluorescent staining. Pretreatment of specific ATM inhibitor (10 microM KU55933) and activator (20 microg/mL chloroquine) before carbon radiation were adopted to explore the involvement of ATM. The roles of ATM were also investigated in its G2/M checkpoint function with histone H3 phosphorylation analysis and flow cytometric assay, and DNA double strand break (DSB) repair function measured using gamma-H2AX foci assay. RESULTS: HRS/IRR was observed with survival and mutation in normal human skin fibroblast cells by carbon ions, while impaired in cells with intrinsic ATM deficiency or normal cells modified with specific ATM activator or inhibitor before irradiation. The dose-response pattern of ATM kinase activation was concordant with the transition from HRS to IRR. The ATM-dependent "early" G2 checkpoint arrest and DNA DSB repair efficiency could explain the difference between HRS and IRR. CONCLUSIONS: These data demonstrate that the HRS/IRR by carbon ion radiation is an ATM-dependent phenomenon in the cellular response to DNA damage. | |||||
| 書誌情報 |
International Journal of Radiation Oncology Biology Physics 巻 75, 号 1, p. 235-243, 発行日 2009-09 |
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| ISSN | ||||||
| 収録物識別子タイプ | ISSN | |||||
| 収録物識別子 | 0360-3016 | |||||
