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SHR Neuro Krebs Kardio Lipid Stoffw Microb

Rinner, B; Gandolfi, G; Meditz, K; Frisch, MT; Wagner, K; Ciarrocchi, A; Torricelli, F; Koivuniemi, R; Niklander, J; Liegl-Atzwanger, B; Lohberger, B; Heitzer, E; Ghaffari-Tabrizi-Wizsy, N; Zweytick, D; Zalaudek, I.
MUG-Mel2, a novel highly pigmented and well characterized NRAS mutated human melanoma cell line.
Sci Rep. 2017; 7(1):2098-2098 Doi: 10.1038/s41598-017-02197-y [OPEN ACCESS]
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Führende Autor*innen der Med Uni Graz
Rinner Beate
Co-Autor*innen der Med Uni Graz
Ghaffari Tabrizi-Wizsy Nassim
Heitzer Ellen
Liegl-Atzwanger Bernadette
Lohberger Birgit
Meditz Katharina
Melcher Marie-Therese
Wagner Karin
Zalaudek Iris
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Abstract:
NRAS mutation in melanoma has been associated with aggressive tumor biology and poor prognosis. Although targeted therapy has been tested for NRAS mutated melanoma, response rates still appear much weaker, than in BRAF mutated melanoma. While plenty of cell lines exist, however, only few melanogenic cell lines retain their in vivo characteristics. In this work we present an intensively pigmented and well-characterized cell line derived from a highly aggressive NRAS mutated cutaneous melanoma, named MUG-Mel2. We present the clinical course, unique morphology, angiogenic properties, growth characteristics using in vivo experiments and 3D cell culture, and results of the exome gene sequencing of an intensively pigmented melanogenic cell line MUG-Mel2, derived from a cutaneous metastasis of an aggressive NRAS p. Q61R mutated melanoma. Amongst several genetic alterations, mutations in GRIN2A, CREBP, PIK3C2G, ATM, and ATR were present. These mutations, known to reinforce DNA repair problems in melanoma, might serve as potential treatment targets. The aggressive and fast growing behavior in animal models and the obtained phenotype in 3D culture reveal a perfect model for research in the field of NRAS mutated melanoma.
Find related publications in this database (using NLM MeSH Indexing)
Cell Culture Techniques - methods
Cell Line, Tumor -
Cells, Cultured -
GTP Phosphohydrolases - genetics
Humans -
Male -
Melanoma - genetics
Melanoma - metabolism
Melanoma - pathology
Membrane Proteins - genetics
Middle Aged -
Mutation, Missense -
Skin Neoplasms - genetics
Skin Neoplasms - metabolism
Skin Neoplasms - pathology
Skin Pigmentation -

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