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Vascular endothelial growth factor receptor-3 expression in mycosis fungoides

  • Ida Holst Pedersen
  • , Andreas Willerslev-Olsen
  • , Claudia Vetter-Kauczok
  • , Thorbjorn Krejsgaard
  • , Britt Lauenborg
  • , Katharina Luise Kopp
  • , Carsten Geisler
  • , Charlotte M. Bonefeld
  • , Qian Zhang
  • , Mariusz A. Wasik
  • , Sally Dabelsteen
  • , Anders Woetmann
  • , Jurgen C. Becker
  • , Niels Odum
  • University of Copenhagen
  • University of Würzburg
  • University of Pennsylvania
  • Graz University of Technology

Research output: Contribution to journalArticlepeer-review

27 Scopus citations

Abstract

Here, we have studied vascular endothelial growth factor receptor-3 (VEGFR-3) expression in mycosis fungoides (MF), the most common type of cutaneous T-cell lymphoma (CTCL). Immunohistochemistry revealed that in two-thirds of 34 patients, VEGFR-3 was expressed in situ by both tumor and stromal cells irrespective of the disease stage. The natural VEGFR-3 ligand, VEGF-C, partially protected malignant T-cell lines from growth inhibition by the histone deacetylase inhibitor, suberoylanilide hydroxamic acid (SAHA). Whereas the malignant T cells did not produce VEGF-C in vitro, its expression was induced during tumor formation in vivo in a xenograft mouse model of MF. In conclusion, malignant and stromal cells express high levels of VEGFR-3 in all stages of MF. Moreover, malignant T cells trigger enhanced VEGF-C expression in fibroblasts, suggesting that cross-talk between tumor and stromal cells plays a role in lymphangiogenesis and possibly disease progression.

Original languageEnglish
Pages (from-to)819-826
Number of pages8
JournalLeukemia and Lymphoma
Volume54
Issue number4
DOIs
StatePublished - Apr 2013
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Angiogenesis
  • CTCL
  • VEGF
  • VEGF-R
  • VEGFR-3

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