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

Nat Commun. 2012 Apr 17:3:783. doi: 10.1038/ncomms1786.

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Hypoxia / radiation effects
  • Cell Line, Tumor
  • Cell Movement / radiation effects
  • Cell Survival / radiation effects
  • Humans
  • Hypoxia-Inducible Factor 1 / metabolism*
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Neoplasms / blood supply
  • Neoplasms / metabolism
  • Neoplasms / physiopathology*
  • Neoplasms / radiotherapy*
  • Radiation Tolerance
  • Tumor Cells, Cultured / cytology
  • Tumor Cells, Cultured / metabolism
  • Xenograft Model Antitumor Assays

Substances

  • Hypoxia-Inducible Factor 1