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      Basal and UV-induced MMP-1 expression are inhibited by p53 in human dermal fibroblasts.

      Experimental Hematology
      Adenoviridae, genetics, Benzothiazoles, pharmacology, Blotting, Western, Cells, Cultured, Dermis, cytology, metabolism, Etoposide, Fibroblasts, drug effects, radiation effects, Humans, Matrix Metalloproteinase 1, Phosphorylation, Proto-Oncogene Proteins c-fos, Proto-Oncogene Proteins c-jun, Toluene, analogs & derivatives, Transduction, Genetic, Tumor Suppressor Protein p53, physiology, Ultraviolet Rays, Young Adult

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          Abstract

          Ultraviolet (UV) triggers induction of matrix metalloproteinase-1 (MMP-1) and also induces the rapid appearance of p53 protein in the epidermis and dermal fibroblasts. However, little is known about the role of p53 on MMP-1 expression in human skin. Here, we investigated the effects of p53 on basal and UV-induced MMP-1 in human dermal fibroblasts. To verify the role of p53 on MMP-1 expression, adenoviral p53 (Ad-p53) gene was infected to human dermal fibroblasts. Our results showed that basal and UV-induced MMP-1 expression was prevented by Ad-p53. In contrast, p53 inhibitor, pifithrin-alpha augmented the UV-induced MMP-1 expression. On the other hand, p53 activator, etoposide, decreased the MMP-1 expression in both normal and p53-overexpressed cells. In addition, MMP-1 expression was not changed by etoposide and/or pifithrin-alpha in HaCaT cells, which have mutation of p53. Taken together, we suggest that p53 inhibits basal and UV-induced MMP-1 expression in human dermal fibroblasts.

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