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A rare coincidence of different types of driver mutations among uterine leiomyomas (UL)
Mutations of mediator subcomplex 12 (MED12) and of high mobility group protein AT-hook 2 (HMGA2) are driver mutations in uterine leiomyomas (UL) that have not been observed to coexist in one tumor and even rarely coexist in different UL tumors of one patient. Here we describe a patient who underwent...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4604635/ https://www.ncbi.nlm.nih.gov/pubmed/26468330 http://dx.doi.org/10.1186/s13039-015-0177-9 |
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author | Holzmann, Carsten Markowski, Dominique Nadine Bartnitzke, Sabine Koczan, Dirk Helmke, Burkhard Maria Bullerdiek, Jörn |
author_facet | Holzmann, Carsten Markowski, Dominique Nadine Bartnitzke, Sabine Koczan, Dirk Helmke, Burkhard Maria Bullerdiek, Jörn |
author_sort | Holzmann, Carsten |
collection | PubMed |
description | Mutations of mediator subcomplex 12 (MED12) and of high mobility group protein AT-hook 2 (HMGA2) are driver mutations in uterine leiomyomas (UL) that have not been observed to coexist in one tumor and even rarely coexist in different UL tumors of one patient. Here we describe a patient who underwent hysterectomy because of multiple leiomyomas which were studied by cytogenetics, MED12 hotspot sequencing, and copy number variation arrays. Two of the UL tumors had different HMGA2 rearrangements not detected by G-banding. Two UL tumors had deletions of the long arm of chromosome 3, in one case associated with a MED12 mutation. Both deletions lead to the loss of MED12L showing strong similarity with MED12. It remains to be determined if this gene can play a role in leiomyomagenesis independent of MED12. In summary, the patient presented exhibits an unusual coincidence of different driver mutations among her leiomyomas. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13039-015-0177-9) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4604635 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-46046352015-10-15 A rare coincidence of different types of driver mutations among uterine leiomyomas (UL) Holzmann, Carsten Markowski, Dominique Nadine Bartnitzke, Sabine Koczan, Dirk Helmke, Burkhard Maria Bullerdiek, Jörn Mol Cytogenet Case Report Mutations of mediator subcomplex 12 (MED12) and of high mobility group protein AT-hook 2 (HMGA2) are driver mutations in uterine leiomyomas (UL) that have not been observed to coexist in one tumor and even rarely coexist in different UL tumors of one patient. Here we describe a patient who underwent hysterectomy because of multiple leiomyomas which were studied by cytogenetics, MED12 hotspot sequencing, and copy number variation arrays. Two of the UL tumors had different HMGA2 rearrangements not detected by G-banding. Two UL tumors had deletions of the long arm of chromosome 3, in one case associated with a MED12 mutation. Both deletions lead to the loss of MED12L showing strong similarity with MED12. It remains to be determined if this gene can play a role in leiomyomagenesis independent of MED12. In summary, the patient presented exhibits an unusual coincidence of different driver mutations among her leiomyomas. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13039-015-0177-9) contains supplementary material, which is available to authorized users. BioMed Central 2015-10-14 /pmc/articles/PMC4604635/ /pubmed/26468330 http://dx.doi.org/10.1186/s13039-015-0177-9 Text en © Holzmann et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Holzmann, Carsten Markowski, Dominique Nadine Bartnitzke, Sabine Koczan, Dirk Helmke, Burkhard Maria Bullerdiek, Jörn A rare coincidence of different types of driver mutations among uterine leiomyomas (UL) |
title | A rare coincidence of different types of driver mutations among uterine leiomyomas (UL) |
title_full | A rare coincidence of different types of driver mutations among uterine leiomyomas (UL) |
title_fullStr | A rare coincidence of different types of driver mutations among uterine leiomyomas (UL) |
title_full_unstemmed | A rare coincidence of different types of driver mutations among uterine leiomyomas (UL) |
title_short | A rare coincidence of different types of driver mutations among uterine leiomyomas (UL) |
title_sort | rare coincidence of different types of driver mutations among uterine leiomyomas (ul) |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4604635/ https://www.ncbi.nlm.nih.gov/pubmed/26468330 http://dx.doi.org/10.1186/s13039-015-0177-9 |
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