Journal of Radiation Research
Online ISSN : 1349-9157
Print ISSN : 0449-3060
Oncology
Beclin1-induced Autophagy Abrogates Radioresistance of Lung Cancer Cells by Suppressing Osteopontin
Seung-Hee CHANGArash MINAI-TEHRANIJi-Young SHINSungjin PARKJi-Eun KIMKyeong-Nam YUSeong-Ho HONGChoong-Man HONGKee-Ho LEEGeorge R BECK JrMyung-Haing CHO
著者情報
ジャーナル オープンアクセス

2012 年 53 巻 3 号 p. 422-432

詳細
抄録
Osteopontin (OPN) serves as an indicator of resistance to radiotherapy. However, the role of OPN in the development of acquired radioresistance in human lung cancer cells has not yet been fully elucidated. Therefore, the potential importance of OPN as a marker of lung cancer with a potential significant role in the development of radioresistance against repeated radiotherapy has prompted us to define the pathways by which OPN regulates lung cancer cell growth. In addition, autophagy has been reported to play a key role in the radiosensitization of cancer cells. Here, we report that increased OPN expression through induction of nuclear p53 following irradiation was inhibited by exogenous beclin-1 (BECN1). Our results clearly show that BECN1 gene expression led to induction of autophagy and inhibition of cancer cell growth and angiogenesis. Our results suggest that the induction of autophagy abrogated the radioresistance of the cancer cells. Interestingly, we showed that knockdown of OPN by lentivirus-mediated shRNA induced the autophagy of human lung cancer cell. Taken together, these results suggest that OPN and BECN1 can be molecular targets for overcoming radioresistance by controlling autophagy.
著者関連情報

この記事は最新の被引用情報を取得できません。

© 2012 by Journal of Radiation Research Editorial Committee
前の記事 次の記事
feedback
Top