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Fibroblasts enhance the invasive capacity of melanoma cells in vitro.

Abstract
In previous experiments we have shown an enhanced expression of matrix metalloproteinase-1 (MMP-1) in fibroblasts obtained from the border of invasive melanoma in comparison to fibroblasts more distant from the tumour. In the study reported here we sought to determine whether melanoma-derived soluble factors are responsible for the stimulation of MMP-1 expression in fibroblasts. By real-time PCR and enzyme-linked immunosorbent assays, we demonstrated that the stimulation of fibroblasts with melanoma cell conditioned medium led to an increased expression of MMP-1 mRNA as well as MMP-1 protein, whereas melanoma cells themselves did not produce detectable amounts of MMP-1 protein. Basic fibroblast growth factor (bFGF) was detected as an important factor responsible for the enhanced expression of MMP-1 by fibroblasts after stimulation with melanoma cell conditioned medium. In a three-dimensional in vitro invasion assay, we demonstrated that fibroblasts are essential for melanoma cell invasion into a collagen I matrix. These findings support the hypothesis that stromal fibroblasts assist the invasion of melanoma cells through the extracellular matrix by producing elevated amounts of proteolytic enzymes after interaction with soluble factors (e.g. bFGF).
AuthorsE Wandel, A Raschke, G Hildebrandt, J Eberle, R Dummer, U Anderegg, A Saalbach
JournalArchives of dermatological research (Arch Dermatol Res) Vol. 293 Issue 12 Pg. 601-8 (Feb 2002) ISSN: 0340-3696 [Print] Germany
PMID11875642 (Publication Type: Journal Article)
Chemical References
  • Collagen Type I
  • Culture Media, Conditioned
  • Gels
  • RNA, Messenger
  • Fibroblast Growth Factor 2
  • Matrix Metalloproteinase 1
Topics
  • Cells, Cultured
  • Collagen Type I
  • Culture Media, Conditioned (pharmacology)
  • Fibroblast Growth Factor 2 (genetics, physiology)
  • Fibroblasts (physiology)
  • Gels
  • Humans
  • Matrix Metalloproteinase 1 (biosynthesis)
  • Melanoma (pathology)
  • Neoplasm Invasiveness
  • RNA, Messenger (metabolism)

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