Cargando…

MUG-Mel2, a novel highly pigmented and well characterized NRAS mutated human melanoma cell line

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Rinner, Beate, Gandolfi, Greta, Meditz, Katharina, Frisch, Marie-Therese, Wagner, Karin, Ciarrocchi, Alessia, Torricelli, Federica, Koivuniemi, Raili, Niklander, Johanna, Liegl-Atzwanger, Bernadette, Lohberger, Birgit, Heitzer, Ellen, Ghaffari-Tabrizi-Wizsy, Nassim, Zweytick, Dagmar, Zalaudek, Iris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5437015/
https://www.ncbi.nlm.nih.gov/pubmed/28522871
http://dx.doi.org/10.1038/s41598-017-02197-y
_version_ 1783237504211615744
author Rinner, Beate
Gandolfi, Greta
Meditz, Katharina
Frisch, Marie-Therese
Wagner, Karin
Ciarrocchi, Alessia
Torricelli, Federica
Koivuniemi, Raili
Niklander, Johanna
Liegl-Atzwanger, Bernadette
Lohberger, Birgit
Heitzer, Ellen
Ghaffari-Tabrizi-Wizsy, Nassim
Zweytick, Dagmar
Zalaudek, Iris
author_facet Rinner, Beate
Gandolfi, Greta
Meditz, Katharina
Frisch, Marie-Therese
Wagner, Karin
Ciarrocchi, Alessia
Torricelli, Federica
Koivuniemi, Raili
Niklander, Johanna
Liegl-Atzwanger, Bernadette
Lohberger, Birgit
Heitzer, Ellen
Ghaffari-Tabrizi-Wizsy, Nassim
Zweytick, Dagmar
Zalaudek, Iris
author_sort Rinner, Beate
collection PubMed
description 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.
format Online
Article
Text
id pubmed-5437015
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-54370152017-05-19 MUG-Mel2, a novel highly pigmented and well characterized NRAS mutated human melanoma cell line Rinner, Beate Gandolfi, Greta Meditz, Katharina Frisch, Marie-Therese Wagner, Karin Ciarrocchi, Alessia Torricelli, Federica Koivuniemi, Raili Niklander, Johanna Liegl-Atzwanger, Bernadette Lohberger, Birgit Heitzer, Ellen Ghaffari-Tabrizi-Wizsy, Nassim Zweytick, Dagmar Zalaudek, Iris Sci Rep Article 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. Nature Publishing Group UK 2017-05-18 /pmc/articles/PMC5437015/ /pubmed/28522871 http://dx.doi.org/10.1038/s41598-017-02197-y Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Rinner, Beate
Gandolfi, Greta
Meditz, Katharina
Frisch, Marie-Therese
Wagner, Karin
Ciarrocchi, Alessia
Torricelli, Federica
Koivuniemi, Raili
Niklander, Johanna
Liegl-Atzwanger, Bernadette
Lohberger, Birgit
Heitzer, Ellen
Ghaffari-Tabrizi-Wizsy, Nassim
Zweytick, Dagmar
Zalaudek, Iris
MUG-Mel2, a novel highly pigmented and well characterized NRAS mutated human melanoma cell line
title MUG-Mel2, a novel highly pigmented and well characterized NRAS mutated human melanoma cell line
title_full MUG-Mel2, a novel highly pigmented and well characterized NRAS mutated human melanoma cell line
title_fullStr MUG-Mel2, a novel highly pigmented and well characterized NRAS mutated human melanoma cell line
title_full_unstemmed MUG-Mel2, a novel highly pigmented and well characterized NRAS mutated human melanoma cell line
title_short MUG-Mel2, a novel highly pigmented and well characterized NRAS mutated human melanoma cell line
title_sort mug-mel2, a novel highly pigmented and well characterized nras mutated human melanoma cell line
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5437015/
https://www.ncbi.nlm.nih.gov/pubmed/28522871
http://dx.doi.org/10.1038/s41598-017-02197-y
work_keys_str_mv AT rinnerbeate mugmel2anovelhighlypigmentedandwellcharacterizednrasmutatedhumanmelanomacellline
AT gandolfigreta mugmel2anovelhighlypigmentedandwellcharacterizednrasmutatedhumanmelanomacellline
AT meditzkatharina mugmel2anovelhighlypigmentedandwellcharacterizednrasmutatedhumanmelanomacellline
AT frischmarietherese mugmel2anovelhighlypigmentedandwellcharacterizednrasmutatedhumanmelanomacellline
AT wagnerkarin mugmel2anovelhighlypigmentedandwellcharacterizednrasmutatedhumanmelanomacellline
AT ciarrocchialessia mugmel2anovelhighlypigmentedandwellcharacterizednrasmutatedhumanmelanomacellline
AT torricellifederica mugmel2anovelhighlypigmentedandwellcharacterizednrasmutatedhumanmelanomacellline
AT koivuniemiraili mugmel2anovelhighlypigmentedandwellcharacterizednrasmutatedhumanmelanomacellline
AT niklanderjohanna mugmel2anovelhighlypigmentedandwellcharacterizednrasmutatedhumanmelanomacellline
AT lieglatzwangerbernadette mugmel2anovelhighlypigmentedandwellcharacterizednrasmutatedhumanmelanomacellline
AT lohbergerbirgit mugmel2anovelhighlypigmentedandwellcharacterizednrasmutatedhumanmelanomacellline
AT heitzerellen mugmel2anovelhighlypigmentedandwellcharacterizednrasmutatedhumanmelanomacellline
AT ghaffaritabriziwizsynassim mugmel2anovelhighlypigmentedandwellcharacterizednrasmutatedhumanmelanomacellline
AT zweytickdagmar mugmel2anovelhighlypigmentedandwellcharacterizednrasmutatedhumanmelanomacellline
AT zalaudekiris mugmel2anovelhighlypigmentedandwellcharacterizednrasmutatedhumanmelanomacellline