Cargando…

Multi-dimensional genomic analysis of myoepithelial carcinoma identifies prevalent oncogenic gene fusions

Myoepithelial carcinoma (MECA) is an aggressive salivary gland cancer with largely unknown genetic features. Here we comprehensively analyze molecular alterations in 40 MECAs using integrated genomic analyses. We identify a low mutational load, and high prevalence (70%) of oncogenic gene fusions. Mo...

Descripción completa

Detalles Bibliográficos
Autores principales: Dalin, Martin G., Katabi, Nora, Persson, Marta, Lee, Ken-Wing, Makarov, Vladimir, Desrichard, Alexis, Walsh, Logan A., West, Lyndsay, Nadeem, Zaineb, Ramaswami, Deepa, Havel, Jonathan J., Kuo, Fengshen, Chadalavada, Kalyani, Nanjangud, Gouri J., Ganly, Ian, Riaz, Nadeem, Ho, Alan L., Antonescu, Cristina R., Ghossein, Ronald, Stenman, Göran, Chan, Timothy A., Morris, Luc G. T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5662567/
https://www.ncbi.nlm.nih.gov/pubmed/29084941
http://dx.doi.org/10.1038/s41467-017-01178-z
_version_ 1783274654560944128
author Dalin, Martin G.
Katabi, Nora
Persson, Marta
Lee, Ken-Wing
Makarov, Vladimir
Desrichard, Alexis
Walsh, Logan A.
West, Lyndsay
Nadeem, Zaineb
Ramaswami, Deepa
Havel, Jonathan J.
Kuo, Fengshen
Chadalavada, Kalyani
Nanjangud, Gouri J.
Ganly, Ian
Riaz, Nadeem
Ho, Alan L.
Antonescu, Cristina R.
Ghossein, Ronald
Stenman, Göran
Chan, Timothy A.
Morris, Luc G. T.
author_facet Dalin, Martin G.
Katabi, Nora
Persson, Marta
Lee, Ken-Wing
Makarov, Vladimir
Desrichard, Alexis
Walsh, Logan A.
West, Lyndsay
Nadeem, Zaineb
Ramaswami, Deepa
Havel, Jonathan J.
Kuo, Fengshen
Chadalavada, Kalyani
Nanjangud, Gouri J.
Ganly, Ian
Riaz, Nadeem
Ho, Alan L.
Antonescu, Cristina R.
Ghossein, Ronald
Stenman, Göran
Chan, Timothy A.
Morris, Luc G. T.
author_sort Dalin, Martin G.
collection PubMed
description Myoepithelial carcinoma (MECA) is an aggressive salivary gland cancer with largely unknown genetic features. Here we comprehensively analyze molecular alterations in 40 MECAs using integrated genomic analyses. We identify a low mutational load, and high prevalence (70%) of oncogenic gene fusions. Most fusions involve the PLAG1 oncogene, which is associated with PLAG1 overexpression. We find FGFR1-PLAG1 in seven (18%) cases, and the novel TGFBR3-PLAG1 fusion in six (15%) cases. TGFBR3-PLAG1 promotes a tumorigenic phenotype in vitro, and is absent in 723 other salivary gland tumors. Other novel PLAG1 fusions include ND4-PLAG1; a fusion between mitochondrial and nuclear DNA. We also identify higher number of copy number alterations as a risk factor for recurrence, independent of tumor stage at diagnosis. Our findings indicate that MECA is a fusion-driven disease, nominate TGFBR3-PLAG1 as a hallmark of MECA, and provide a framework for future diagnostic and therapeutic research in this lethal cancer.
format Online
Article
Text
id pubmed-5662567
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-56625672017-11-01 Multi-dimensional genomic analysis of myoepithelial carcinoma identifies prevalent oncogenic gene fusions Dalin, Martin G. Katabi, Nora Persson, Marta Lee, Ken-Wing Makarov, Vladimir Desrichard, Alexis Walsh, Logan A. West, Lyndsay Nadeem, Zaineb Ramaswami, Deepa Havel, Jonathan J. Kuo, Fengshen Chadalavada, Kalyani Nanjangud, Gouri J. Ganly, Ian Riaz, Nadeem Ho, Alan L. Antonescu, Cristina R. Ghossein, Ronald Stenman, Göran Chan, Timothy A. Morris, Luc G. T. Nat Commun Article Myoepithelial carcinoma (MECA) is an aggressive salivary gland cancer with largely unknown genetic features. Here we comprehensively analyze molecular alterations in 40 MECAs using integrated genomic analyses. We identify a low mutational load, and high prevalence (70%) of oncogenic gene fusions. Most fusions involve the PLAG1 oncogene, which is associated with PLAG1 overexpression. We find FGFR1-PLAG1 in seven (18%) cases, and the novel TGFBR3-PLAG1 fusion in six (15%) cases. TGFBR3-PLAG1 promotes a tumorigenic phenotype in vitro, and is absent in 723 other salivary gland tumors. Other novel PLAG1 fusions include ND4-PLAG1; a fusion between mitochondrial and nuclear DNA. We also identify higher number of copy number alterations as a risk factor for recurrence, independent of tumor stage at diagnosis. Our findings indicate that MECA is a fusion-driven disease, nominate TGFBR3-PLAG1 as a hallmark of MECA, and provide a framework for future diagnostic and therapeutic research in this lethal cancer. Nature Publishing Group UK 2017-10-30 /pmc/articles/PMC5662567/ /pubmed/29084941 http://dx.doi.org/10.1038/s41467-017-01178-z 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
Dalin, Martin G.
Katabi, Nora
Persson, Marta
Lee, Ken-Wing
Makarov, Vladimir
Desrichard, Alexis
Walsh, Logan A.
West, Lyndsay
Nadeem, Zaineb
Ramaswami, Deepa
Havel, Jonathan J.
Kuo, Fengshen
Chadalavada, Kalyani
Nanjangud, Gouri J.
Ganly, Ian
Riaz, Nadeem
Ho, Alan L.
Antonescu, Cristina R.
Ghossein, Ronald
Stenman, Göran
Chan, Timothy A.
Morris, Luc G. T.
Multi-dimensional genomic analysis of myoepithelial carcinoma identifies prevalent oncogenic gene fusions
title Multi-dimensional genomic analysis of myoepithelial carcinoma identifies prevalent oncogenic gene fusions
title_full Multi-dimensional genomic analysis of myoepithelial carcinoma identifies prevalent oncogenic gene fusions
title_fullStr Multi-dimensional genomic analysis of myoepithelial carcinoma identifies prevalent oncogenic gene fusions
title_full_unstemmed Multi-dimensional genomic analysis of myoepithelial carcinoma identifies prevalent oncogenic gene fusions
title_short Multi-dimensional genomic analysis of myoepithelial carcinoma identifies prevalent oncogenic gene fusions
title_sort multi-dimensional genomic analysis of myoepithelial carcinoma identifies prevalent oncogenic gene fusions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5662567/
https://www.ncbi.nlm.nih.gov/pubmed/29084941
http://dx.doi.org/10.1038/s41467-017-01178-z
work_keys_str_mv AT dalinmarting multidimensionalgenomicanalysisofmyoepithelialcarcinomaidentifiesprevalentoncogenicgenefusions
AT katabinora multidimensionalgenomicanalysisofmyoepithelialcarcinomaidentifiesprevalentoncogenicgenefusions
AT perssonmarta multidimensionalgenomicanalysisofmyoepithelialcarcinomaidentifiesprevalentoncogenicgenefusions
AT leekenwing multidimensionalgenomicanalysisofmyoepithelialcarcinomaidentifiesprevalentoncogenicgenefusions
AT makarovvladimir multidimensionalgenomicanalysisofmyoepithelialcarcinomaidentifiesprevalentoncogenicgenefusions
AT desrichardalexis multidimensionalgenomicanalysisofmyoepithelialcarcinomaidentifiesprevalentoncogenicgenefusions
AT walshlogana multidimensionalgenomicanalysisofmyoepithelialcarcinomaidentifiesprevalentoncogenicgenefusions
AT westlyndsay multidimensionalgenomicanalysisofmyoepithelialcarcinomaidentifiesprevalentoncogenicgenefusions
AT nadeemzaineb multidimensionalgenomicanalysisofmyoepithelialcarcinomaidentifiesprevalentoncogenicgenefusions
AT ramaswamideepa multidimensionalgenomicanalysisofmyoepithelialcarcinomaidentifiesprevalentoncogenicgenefusions
AT haveljonathanj multidimensionalgenomicanalysisofmyoepithelialcarcinomaidentifiesprevalentoncogenicgenefusions
AT kuofengshen multidimensionalgenomicanalysisofmyoepithelialcarcinomaidentifiesprevalentoncogenicgenefusions
AT chadalavadakalyani multidimensionalgenomicanalysisofmyoepithelialcarcinomaidentifiesprevalentoncogenicgenefusions
AT nanjangudgourij multidimensionalgenomicanalysisofmyoepithelialcarcinomaidentifiesprevalentoncogenicgenefusions
AT ganlyian multidimensionalgenomicanalysisofmyoepithelialcarcinomaidentifiesprevalentoncogenicgenefusions
AT riaznadeem multidimensionalgenomicanalysisofmyoepithelialcarcinomaidentifiesprevalentoncogenicgenefusions
AT hoalanl multidimensionalgenomicanalysisofmyoepithelialcarcinomaidentifiesprevalentoncogenicgenefusions
AT antonescucristinar multidimensionalgenomicanalysisofmyoepithelialcarcinomaidentifiesprevalentoncogenicgenefusions
AT ghosseinronald multidimensionalgenomicanalysisofmyoepithelialcarcinomaidentifiesprevalentoncogenicgenefusions
AT stenmangoran multidimensionalgenomicanalysisofmyoepithelialcarcinomaidentifiesprevalentoncogenicgenefusions
AT chantimothya multidimensionalgenomicanalysisofmyoepithelialcarcinomaidentifiesprevalentoncogenicgenefusions
AT morrislucgt multidimensionalgenomicanalysisofmyoepithelialcarcinomaidentifiesprevalentoncogenicgenefusions