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KRAS mutation in papillary fibroelastoma: a true cardiac neoplasm?

Primary cardiac tumours are rare and mostly benign lesions. Recent publications report that cardiac papillary fibroelastomas are the most common benign primary heart tumour, outnumbering myxomas. However, there is no consensus about their aetiology. We investigated the molecular profile of these tum...

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Autores principales: Wittersheim, Maike, Heydt, Carina, Hoffmann, Fabian, Büttner, Reinhard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5402176/
https://www.ncbi.nlm.nih.gov/pubmed/28451458
http://dx.doi.org/10.1002/cjp2.66
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author Wittersheim, Maike
Heydt, Carina
Hoffmann, Fabian
Büttner, Reinhard
author_facet Wittersheim, Maike
Heydt, Carina
Hoffmann, Fabian
Büttner, Reinhard
author_sort Wittersheim, Maike
collection PubMed
description Primary cardiac tumours are rare and mostly benign lesions. Recent publications report that cardiac papillary fibroelastomas are the most common benign primary heart tumour, outnumbering myxomas. However, there is no consensus about their aetiology. We investigated the molecular profile of these tumours using next generation sequencing in a cohort of 16 cases. Eleven of 14 (79%) analysable tumours showed mutations of the KRAS oncogene. Our results provide unambiguous evidence that a significant proportion of these lesions are genuine neoplastic tumours caused by an oncogenic driver mutation.
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spelling pubmed-54021762017-04-27 KRAS mutation in papillary fibroelastoma: a true cardiac neoplasm? Wittersheim, Maike Heydt, Carina Hoffmann, Fabian Büttner, Reinhard J Pathol Clin Res Brief Definitive Report Primary cardiac tumours are rare and mostly benign lesions. Recent publications report that cardiac papillary fibroelastomas are the most common benign primary heart tumour, outnumbering myxomas. However, there is no consensus about their aetiology. We investigated the molecular profile of these tumours using next generation sequencing in a cohort of 16 cases. Eleven of 14 (79%) analysable tumours showed mutations of the KRAS oncogene. Our results provide unambiguous evidence that a significant proportion of these lesions are genuine neoplastic tumours caused by an oncogenic driver mutation. John Wiley and Sons Inc. 2017-03-07 /pmc/articles/PMC5402176/ /pubmed/28451458 http://dx.doi.org/10.1002/cjp2.66 Text en © 2017 The Authors The Journal of Pathology: Clinical Research published by The Pathological Society of Great Britain and Ireland and John Wiley & Sons Ltd This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Brief Definitive Report
Wittersheim, Maike
Heydt, Carina
Hoffmann, Fabian
Büttner, Reinhard
KRAS mutation in papillary fibroelastoma: a true cardiac neoplasm?
title KRAS mutation in papillary fibroelastoma: a true cardiac neoplasm?
title_full KRAS mutation in papillary fibroelastoma: a true cardiac neoplasm?
title_fullStr KRAS mutation in papillary fibroelastoma: a true cardiac neoplasm?
title_full_unstemmed KRAS mutation in papillary fibroelastoma: a true cardiac neoplasm?
title_short KRAS mutation in papillary fibroelastoma: a true cardiac neoplasm?
title_sort kras mutation in papillary fibroelastoma: a true cardiac neoplasm?
topic Brief Definitive Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5402176/
https://www.ncbi.nlm.nih.gov/pubmed/28451458
http://dx.doi.org/10.1002/cjp2.66
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