The Journal of Dermatology · 2006 · 12 citations · 17 references
MedicineCell BiologyDermatologyCutaneous OncologyTumor MicroenvironmentTumor ProgressionBasal Cell CarcinomaCancer-associated FibroblastsExtracellular MatrixNeoplastic Skin LesionsSkin TumorsDermal Host DefenseDermal-epidermal InteractionsEpidermal CellsFibroblast CultureMatrix Metalloproteinase Gene ExpressionMatrix Metalloproteinase Gene RegulationMatrix Metalloproteinase ModulationMatrix Metalloproteinases
To address whether matrix metalloproteinase (MMP)-2 expression by mesenchymal fibroblasts may be differentially modulated by interactions with normal or malignant epidermal cells, we set up a fibroblast co-culture model separately with keratinocytes, basal cell carcinoma cells and melanoma cells. Real-time reverse transcription polymerase chain reaction (RT-PCR) and gelatin zymography were used to detect and quantify the expression of MMP-2 by these different kinds of cells. In independent cultures, MMP-2 was highly expressed by fibroblasts and melanoma cells constitutively, but barely expressed by keratinocytes and basal cell carcinoma (BCC) cells. MMP-2 expression by fibroblasts was downregulated in co-cultures with keratinocytes or BCC cells, but not with melanoma cells. These results indicate that epidermal-mesenchymal interactions are important modulators for MMP-2 expression by cutaneous cells and suggest a host-defense mechanism against the tumor progression of BCC.
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Reduced angiogenesis and tumor progression in gelatinase A-deficient mice.
Takeshi Itoh, Masatoshi Tanioka, Hiroki Yoshida et al. · PubMed · 1998 · 878 citations
Medicine, Cancer Biology, Oncology +15
Interstitial collagenases as markers of tumor progression.
Constance Brinckerhoff, Joni L. Rutter, Ulrike Benbow · PubMed · 2000 · 335 citations