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サイトウ タイイチ
SAITO Taiichi
齋藤 太一 所属 医学研究科 医学研究科 (医学部医学科をご参照ください) 職種 非常勤講師 |
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| 論文種別 | 原著 |
| 言語種別 | 英語 |
| 査読の有無 | 査読あり |
| 表題 | Retinoblastoma protein prevents staurosporine-induced cell death in a retinoblastoma-defective human glioma cell line. |
| 掲載誌名 | 正式名:Pathobiology : journal of immunopathology, molecular and cellular biology 略 称:Pathobiology ISSNコード:1015-2008(Print)1015-2008(Linking) |
| 掲載区分 | 国外 |
| 巻・号・頁 | 74(1),pp.22-31 |
| 著者・共著者 | Yamasaki Fumiyuki, Kajiwara Yoshinori, Hama Seiji, Murakami Taro, Hidaka Toshikazu, Saito Taiichi, Yoshioka Hiroyuki, Sugiyama Kazuhiko, Arita Kazunori, Kurisu Kaoru |
| 発行年月 | 2007/07 |
| 概要 | OBJECTIVE:To investigate the mechanism of staurosporine-induced glioma cell death and cell cycle arrest using adenovirus-mediated gene transfection, as well as the function of retinoblastoma (Rb) and genetic instability induced by staurosporine.METHODS:Cell cycle regulation, cell death and nuclear abnormalities induced by staurosporine were examined using an adenovirus vector expressing Rb, p16 or p21 genes in human glioma cell lines.RESULTS:The Rb-defective SF-539 cell line was resistant to staurosporine compared with cell lines expressing intact Rb. SF-539 glioma cells exposed to staurosporine became multinucleated and then died. Multinucleation was prevented in SF-539 cells transfected with the Rb gene, thus decreasing the death rate of these cells.CONCLUSIONS:These results imply that enforced Rb expression protects cells from genomic instability induced by staurosporine regardless of its upstream molecular effects. |
| DOI | 10.1159/000101048 |
| 文献番号 | 17496430 |