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    L. Feuerer, S. Lamm, I. Henz, Melanie Kappelmann-Fenzl, S. Haferkamp, S. Meierjohann, C. Hellerbrand, S. Kuphal, A. Bosserhoff

    Role of MIA (melanoma inhibitory activity) in melanocyte senescence

    Pigment Cell & Melanoma Research, no. First Published: 06 June 2019


    DOI: 10.1111/pcmr.12801

    Abstract anzeigen

    The protein MIA is known to be expressed in melanoma and to support melanoma progression. Interestingly, previous studies also observed the expression of MIA in nevi. Concentrating on these findings, we revealed that MIA expression is correlated with a senescent state in melanocytes. Induction of replicative or oncogene‐induced senescence resulted in increased MIA expression in vitro. Notably, MIA‐knockdown in senescent melanocytes reduced the percentage of senescence‐associated beta‐Gal‐positive cells and enhanced proliferation. Using the melanoma mouse model Tg(Grm1), MIA‐deficient mice supported the impact of MIA on senescence by showing a significantly earlier tumor onset compared to controls. In melanocytes, MIA‐knockdown led to a downregulation of the cell cycle inhibitor p21 in vitro and in vivo. In contrast, after induction of hTERT in human melanoma cells, p21 regulation by MIA was lost. In summary, our data show for the first time that MIA is a regulator of cellular senescence in human and murine melanocytes.