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Insulin receptor activation in solitary fibrous tumours

  • Y. Li
  • , Q. Chang
  • , B. P. Rubin
  • , C. D.M. Fletcher
  • , T. W. Morgan
  • , S. J. Metzer
  • , D. J. Sugarbaker
  • , J. A. Fletcher
  • , S. Xiao*
  • *Corresponding author for this work
  • Brigham and Women’s Hospital

Research output: Contribution to journalArticlepeer-review

Abstract

Solitary fibrous tumours (SFTs) are known to overexpress insulin-like growth factor 2 (IGF-2). The down-stream oncogenic pathways of IGF-2, however, are not clear. Here we report uniform activation of the insulin receptor (IR) pathway in SFTs, which are mesenchymal tumours frequently associated with hypoglycaemia. Whereas the IR and its downstream signalling pathways were constitutively activated in SFTs, insulin-like growth factor 1 receptor (IGF-1R) was not expressed in these tumours. We also find that SFT cells secrete IGF-2 and proliferate in serum-free medium, consistent with an IGF-2/IR autocrine loop. The aetiological relevance of IGF-2 is supported by expression of IR-A, the IR isoform with high affinity for IGF-2, in all SFTs. Our studies suggest that IR activation plays an oncogenic role in SFTs.

Original languageEnglish
Pages (from-to)550-554
Number of pages5
JournalJournal of Pathology
Volume211
Issue number5
DOIs
StatePublished - Apr 2007
Externally publishedYes

Keywords

  • IGF-2
  • Insulin receptor
  • Solitary fibrous tumour

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