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

Author

Listed:
  • Hiroshi Harada

    (Group of Radiation and Tumor Biology, Career-Path Promotion Unit for Young Life Scientists, Kyoto University, Yoshida Konoe-cho
    Kyoto University Graduate School of Medicine)

  • Masahiro Inoue

    (Osaka Medical Center for Cancer and Cardiovascular Diseases)

  • Satoshi Itasaka

    (Kyoto University Graduate School of Medicine)

  • Kiichi Hirota

    (Kyoto University Hospital, Kyoto University)

  • Akiyo Morinibu

    (Group of Radiation and Tumor Biology, Career-Path Promotion Unit for Young Life Scientists, Kyoto University, Yoshida Konoe-cho)

  • Kazumi Shinomiya

    (Group of Radiation and Tumor Biology, Career-Path Promotion Unit for Young Life Scientists, Kyoto University, Yoshida Konoe-cho)

  • Lihua Zeng

    (Group of Radiation and Tumor Biology, Career-Path Promotion Unit for Young Life Scientists, Kyoto University, Yoshida Konoe-cho
    Kyoto University Graduate School of Medicine
    Fourth Military Medical University, 17 Changle West Road, Xi'an, Shaanxi 710032, China.)

  • Guangfei Ou

    (Kyoto University Graduate School of Medicine)

  • Yuxi Zhu

    (Group of Radiation and Tumor Biology, Career-Path Promotion Unit for Young Life Scientists, Kyoto University, Yoshida Konoe-cho
    Kyoto University Graduate School of Medicine)

  • Michio Yoshimura

    (Kyoto University Graduate School of Medicine
    Gray Institute for Radiation Oncology and Biology, University of Oxford)

  • W. Gillies McKenna

    (Gray Institute for Radiation Oncology and Biology, University of Oxford)

  • Ruth J. Muschel

    (Gray Institute for Radiation Oncology and Biology, University of Oxford)

  • Masahiro Hiraoka

    (Kyoto University Graduate School of Medicine)

Abstract

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.

Suggested Citation

  • Hiroshi Harada & Masahiro Inoue & Satoshi Itasaka & Kiichi Hirota & Akiyo Morinibu & Kazumi Shinomiya & Lihua Zeng & Guangfei Ou & Yuxi Zhu & Michio Yoshimura & W. Gillies McKenna & Ruth J. Muschel & , 2012. "Cancer cells that survive radiation therapy acquire HIF-1 activity and translocate towards tumour blood vessels," Nature Communications, Nature, vol. 3(1), pages 1-12, January.
  • Handle: RePEc:nat:natcom:v:3:y:2012:i:1:d:10.1038_ncomms1786
    DOI: 10.1038/ncomms1786
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