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Hotspots of MLV integration in the hematopoietic tumor genome

Extensive research has been performed regarding the integration sites of murine leukemia retrovirus (MLV) for the identification of proto-oncogenes. To date, the overlap of mutations within specific oligonucleotides across different tumor genomes has been regarded as a rare event; however, a recent...

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Autores principales: Tsuruyama, T, Hiratsuka, T, Yamada, N
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5340798/
https://www.ncbi.nlm.nih.gov/pubmed/27721401
http://dx.doi.org/10.1038/onc.2016.285
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author Tsuruyama, T
Hiratsuka, T
Yamada, N
author_facet Tsuruyama, T
Hiratsuka, T
Yamada, N
author_sort Tsuruyama, T
collection PubMed
description Extensive research has been performed regarding the integration sites of murine leukemia retrovirus (MLV) for the identification of proto-oncogenes. To date, the overlap of mutations within specific oligonucleotides across different tumor genomes has been regarded as a rare event; however, a recent study of MLV integration into the oncogene Zfp521 suggested the existence of a hotspot oligonucleotide for MLV integration. In the current review, we discuss the hotspots of MLV integration into several genes: c-Myc, Stat5a and N-myc, as well as ZFP521, as examined in tumor genomes. From this, MLV integration convergence within specific oligonucleotides is not necessarily a rare event. This short review aims to promote re-consideration of MLV integration within the tumor genome, which involves both well-known and potentially newly identified and novel mechanisms and specifications.
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spelling pubmed-53407982017-03-21 Hotspots of MLV integration in the hematopoietic tumor genome Tsuruyama, T Hiratsuka, T Yamada, N Oncogene Review Extensive research has been performed regarding the integration sites of murine leukemia retrovirus (MLV) for the identification of proto-oncogenes. To date, the overlap of mutations within specific oligonucleotides across different tumor genomes has been regarded as a rare event; however, a recent study of MLV integration into the oncogene Zfp521 suggested the existence of a hotspot oligonucleotide for MLV integration. In the current review, we discuss the hotspots of MLV integration into several genes: c-Myc, Stat5a and N-myc, as well as ZFP521, as examined in tumor genomes. From this, MLV integration convergence within specific oligonucleotides is not necessarily a rare event. This short review aims to promote re-consideration of MLV integration within the tumor genome, which involves both well-known and potentially newly identified and novel mechanisms and specifications. Nature Publishing Group 2017-03-02 2016-11-07 /pmc/articles/PMC5340798/ /pubmed/27721401 http://dx.doi.org/10.1038/onc.2016.285 Text en Copyright © 2017 The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Review
Tsuruyama, T
Hiratsuka, T
Yamada, N
Hotspots of MLV integration in the hematopoietic tumor genome
title Hotspots of MLV integration in the hematopoietic tumor genome
title_full Hotspots of MLV integration in the hematopoietic tumor genome
title_fullStr Hotspots of MLV integration in the hematopoietic tumor genome
title_full_unstemmed Hotspots of MLV integration in the hematopoietic tumor genome
title_short Hotspots of MLV integration in the hematopoietic tumor genome
title_sort hotspots of mlv integration in the hematopoietic tumor genome
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5340798/
https://www.ncbi.nlm.nih.gov/pubmed/27721401
http://dx.doi.org/10.1038/onc.2016.285
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