Cancer cells that survive radiation therapy acquire HIF-1 activity and translocate towards tumour blood vessels

被引:155
作者
Harada, Hiroshi [1 ,2 ]
Inoue, Masahiro [3 ]
Itasaka, Satoshi [2 ]
Hirota, Kiichi [4 ]
Morinibu, Akiyo [1 ]
Shinomiya, Kazumi [1 ]
Zeng, Lihua [1 ,2 ,5 ]
Ou, Guangfei [2 ]
Zhu, Yuxi [1 ,2 ]
Yoshimura, Michio [2 ,6 ]
McKenna, W. Gillies [6 ]
Muschel, Ruth J. [6 ]
Hiraoka, Masahiro [2 ]
机构
[1] Kyoto Univ, Grp Radiat & Tumor Biol, Career Path Promot Unit Young Life Scientists, Sakyo Ku, Kyoto 6068501, Japan
[2] Kyoto Univ, Grad Sch Med, Dept Radiat Oncol & Image Appl Therapy, Sakyo Ku, Kyoto 6068507, Japan
[3] Osaka Med Ctr Canc & Cardiovasc Dis, Dept Biochem, Higashinari Ku, Osaka 5378511, Japan
[4] Kyoto Univ, Dept Anesthesia, Kyoto Univ Hosp, Sakyo Ku, Kyoto 6068507, Japan
[5] Fourth Mil Med Univ, Dept Radiat Med, Xian 710032, Shaanxi, Peoples R China
[6] Univ Oxford, Gray Inst Radiat Oncol & Biol, Oxford OX3 7DQ, England
基金
日本学术振兴会;
关键词
HYPOXIA-INDUCIBLE FACTOR-1; FACTOR-I; INTERMITTENT HYPOXIA; RECOMBINASE ACTIVITY; MAMMALIAN-CELLS; CRE RECOMBINASE; FREE-RADICALS; EXPRESSION; OXYGEN; RADIOSENSITIVITY;
D O I
10.1038/ncomms1786
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Tumour recurrence frequently occurs after radiotherapy, but the characteristics, intratumoural localization and post-irradiation behaviour of radioresistant cancer cells remain largely unknown. Here we develop a sophisticated strategy to track the post-irradiation fate of the cells, which exist in perinecrotic regions at the time of radiation. Although the perinecrotic tumour cells are originally hypoxia-inducible factor 1 (HIF-1)-negative, they acquire HIF-1 activity after surviving radiation, which triggers their translocation towards tumour blood vessels. HIF-1 inhibitors suppress the translocation and decrease the incidence of post-irradiation tumour recurrence. For the first time, our data unveil the HIF-1-dependent cellular dynamics during post-irradiation tumour recurrence and provide a rational basis for targeting HIF-1 after radiation therapy.
引用
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页数:10
相关论文
共 52 条
[1]   Hypoxia-inducible factor-1α (HIF-1α) escapes O2-driven proteasomal degradation irrespective of its subcellular localization:: nucleus or cytoplasm [J].
Berra, E ;
Roux, D ;
Richard, DE ;
Pouysségur, J .
EMBO REPORTS, 2001, 2 (07) :615-620
[2]   Cell cycle kinase inhibitor expression and hypoxia-induced cell cycle arrest in human cancer cell lines [J].
Box, AH ;
Demetrick, DJ .
CARCINOGENESIS, 2004, 25 (12) :2325-2335
[3]   Hypoxia, DNA repair and genetic instability [J].
Bristow, Robert G. ;
Hill, Richard P. .
NATURE REVIEWS CANCER, 2008, 8 (03) :180-192
[4]   Exploiting tumour hypoxia in cancer treatment [J].
Brown, JM ;
William, WR .
NATURE REVIEWS CANCER, 2004, 4 (06) :437-447
[5]   Tumor hypoxia at the micro-regional level: clinical relevance and predictive value of exogenous and endogenous hypoxic cell markers [J].
Bussink, J ;
Kaanders, JHAM ;
van der Kogel, AJ .
RADIOTHERAPY AND ONCOLOGY, 2003, 67 (01) :3-15
[6]   Hypoxia, gene expression, and metastasis [J].
Chan, Denise A. ;
Giaccia, Amato J. .
CANCER AND METASTASIS REVIEWS, 2007, 26 (02) :333-339
[7]   Chronic hypoxia decreases synthesis of homologous recombination proteins to offset chemoresistance and radioresistance [J].
Chan, Norman ;
Koritzinsky, Marianne ;
Zhao, Helen ;
Bindra, Ranjit ;
Glazer, Peter M. ;
Powell, Simon ;
Belmaaza, Abdellah ;
Wouters, Brad ;
Bristow, Robert G. .
CANCER RESEARCH, 2008, 68 (02) :605-614
[8]   HIGH-EFFICIENCY TRANSFORMATION OF MAMMALIAN-CELLS BY PLASMID DNA [J].
CHEN, C ;
OKAYAMA, H .
MOLECULAR AND CELLULAR BIOLOGY, 1987, 7 (08) :2745-2752
[9]   INFLUENCE OF OXYGEN TENSION ON X-RAY-INDUCED CHROMOSOMAL DAMAGE IN EHRLICH ASCITES TUMOR CELLS IRRADIATED INVITRO AND INVIVO [J].
DESCHNER, EE ;
GRAY, LH .
RADIATION RESEARCH, 1959, 11 (01) :115-146
[10]   Cycling hypoxia and free radicals regulate angiogenesis and radiotherapy response [J].
Dewhirst, Mark W. ;
Cao, Yiting ;
Moeller, Benjamin .
NATURE REVIEWS CANCER, 2008, 8 (06) :425-437