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Down's syndrome suppression of tumour growth and the role of the calcineurin inhibitor DSCR1.

The incidence of many cancer types is significantly reduced in individuals with Down's syndrome, and it is thought that this broad cancer protection is conferred by the increased expression of one or more of the 231 supernumerary genes on the extra copy of chromosome 21. One such gene is Down's syndrome candidate region-1 (DSCR1, also known as RCAN1), which encodes a protein that suppresses vascular endothelial growth factor (VEGF)-mediated angiogenic signalling by the calcineurin pathway. Here we show that DSCR1 is increased in Down's syndrome tissues and in a mouse model of Down's syndrome. Furthermore, we show that the modest increase in expression afforded by a single extra transgenic copy of Dscr1 is sufficient to confer significant suppression of tumour growth in mice, and that such resistance is a consequence of a deficit in tumour angiogenesis arising from suppression of the calcineurin pathway. We also provide evidence that attenuation of calcineurin activity by DSCR1, together with another chromosome 21 gene Dyrk1a, may be sufficient to markedly diminish angiogenesis. These data provide a mechanism for the reduced cancer incidence in Down's syndrome and identify the calcineurin signalling pathway, and its regulators DSCR1 and DYRK1A, as potential therapeutic targets in cancers arising in all individuals.

Pubmed ID: 19458618

Authors

  • Baek KH
  • Zaslavsky A
  • Lynch RC
  • Britt C
  • Okada Y
  • Siarey RJ
  • Lensch MW
  • Park IH
  • Yoon SS
  • Minami T
  • Korenberg JR
  • Folkman J
  • Daley GQ
  • Aird WC
  • Galdzicki Z
  • Ryeom S

Journal

Nature

Publication Data

June 25, 2009

Associated Grants

  • Agency: NCI NIH HHS, Id: R01 CA118374
  • Agency: NCI NIH HHS, Id: R01 CA118374-01A2
  • Agency: Howard Hughes Medical Institute, Id:

Mesh Terms

  • Animals
  • Calcineurin
  • Catechols
  • Cells, Cultured
  • Disease Models, Animal
  • Down Syndrome
  • Endothelial Cells
  • Gene Dosage
  • Humans
  • Inositol
  • Intracellular Signaling Peptides and Proteins
  • Mice
  • Mice, Transgenic
  • Muscle Proteins
  • Protein-Serine-Threonine Kinases
  • Protein-Tyrosine Kinases