論文

査読有り
2009年

Novel Function of Transcription Factor ATF5: Blockade of p53-dependent Apoptosis Induced by Ionizing Irradiation

CELL STRUCTURE AND FUNCTION
  • Takeshi Nishioka
  • ,
  • Yusuke Miyai
  • ,
  • Hisashi Haga
  • ,
  • Kazushige Kawabata
  • ,
  • Hiroki Shirato
  • ,
  • Akihiro Homma
  • ,
  • Kenichiro Shibata
  • ,
  • Motoaki Yasuda

34
1
開始ページ
17
終了ページ
22
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1247/csf.08041
出版者・発行元
JAPAN SOC CELL BIOLOGY

Purpose: To find a new molecule that affects p53-dependent radiosensitivity.Methods and Materials: A mouse sarcoma cell line, QRsP(p53+/+), was used. From this cell line, we established a radiosensitive clone and a radioresistant one. Colony assay, p53 gene transfer, a luciferase assay for p53 and p21, animal transplantation experiment, and DNA array analyses were performed.Results: Microarray showed marked reduction of a transcription factor, ATF5, both in vitro and in vivo for the radiosensitive clone. Interestingly, flow cytometric analysis demonstrated marked apoptosis for the radiosensitive clone by p53 cloned adenovirus infection. Luciferase reporter assay revealed that ATF5 suppressed the transactivational activity of p53 and p63. By ATF5 gene transfer, the radiosensitive clone regained resistance to both ionizing-radiation and Ad-p53 infection-induced cell death. Surprisingly, time-lapse cell migration observation revealed greater cell motility for ATF5-transfected radiosensitive clone.Conclusions: It seems likely that ATF5 is a potent repressor of p53 and elevated expression of ATF5 in a tumor may relate to enhanced malignant phenotypes, such as radioresistance or greater cell motility.

リンク情報
DOI
https://doi.org/10.1247/csf.08041
CiNii Articles
http://ci.nii.ac.jp/naid/40017160761
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000267879000003&DestApp=WOS_CPL
ID情報
  • DOI : 10.1247/csf.08041
  • ISSN : 0386-7196
  • eISSN : 1347-3700
  • CiNii Articles ID : 40017160761
  • Web of Science ID : WOS:000267879000003

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