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Identification of a pan-cancer oncogenic microRNA superfamily anchored by a central core seed motif
MicroRNAs modulate tumorigenesis through suppression of specific genes. As many tumour types rely on overlapping oncogenic pathways, a core set of microRNAs may exist, which consistently drives or suppresses tumorigenesis in many cancer types. Here we integrate The Cancer Genome Atlas (TCGA) pan-can...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Pub. Group
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3868236/ https://www.ncbi.nlm.nih.gov/pubmed/24220575 http://dx.doi.org/10.1038/ncomms3730 |
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author | Hamilton, Mark P. Rajapakshe, Kimal Hartig, Sean M. Reva, Boris McLellan, Michael D. Kandoth, Cyriac Ding, Li Zack, Travis I. Gunaratne, Preethi H. Wheeler, David A. Coarfa, Cristian McGuire, Sean E. |
author_facet | Hamilton, Mark P. Rajapakshe, Kimal Hartig, Sean M. Reva, Boris McLellan, Michael D. Kandoth, Cyriac Ding, Li Zack, Travis I. Gunaratne, Preethi H. Wheeler, David A. Coarfa, Cristian McGuire, Sean E. |
author_sort | Hamilton, Mark P. |
collection | PubMed |
description | MicroRNAs modulate tumorigenesis through suppression of specific genes. As many tumour types rely on overlapping oncogenic pathways, a core set of microRNAs may exist, which consistently drives or suppresses tumorigenesis in many cancer types. Here we integrate The Cancer Genome Atlas (TCGA) pan-cancer data set with a microRNA target atlas composed of publicly available Argonaute Crosslinking Immunoprecipitation (AGO-CLIP) data to identify pan-tumour microRNA drivers of cancer. Through this analysis, we show a pan-cancer, coregulated oncogenic microRNA ‘superfamily’ consisting of the miR-17, miR-19, miR-130, miR-93, miR-18, miR-455 and miR-210 seed families, which cotargets critical tumour suppressors via a central GUGC core motif. We subsequently define mutations in microRNA target sites using the AGO-CLIP microRNA target atlas and TCGA exome-sequencing data. These combined analyses identify pan-cancer oncogenic cotargeting of the phosphoinositide 3-kinase, TGFβ and p53 pathways by the miR-17-19-130 superfamily members. |
format | Online Article Text |
id | pubmed-3868236 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Nature Pub. Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-38682362013-12-20 Identification of a pan-cancer oncogenic microRNA superfamily anchored by a central core seed motif Hamilton, Mark P. Rajapakshe, Kimal Hartig, Sean M. Reva, Boris McLellan, Michael D. Kandoth, Cyriac Ding, Li Zack, Travis I. Gunaratne, Preethi H. Wheeler, David A. Coarfa, Cristian McGuire, Sean E. Nat Commun Article MicroRNAs modulate tumorigenesis through suppression of specific genes. As many tumour types rely on overlapping oncogenic pathways, a core set of microRNAs may exist, which consistently drives or suppresses tumorigenesis in many cancer types. Here we integrate The Cancer Genome Atlas (TCGA) pan-cancer data set with a microRNA target atlas composed of publicly available Argonaute Crosslinking Immunoprecipitation (AGO-CLIP) data to identify pan-tumour microRNA drivers of cancer. Through this analysis, we show a pan-cancer, coregulated oncogenic microRNA ‘superfamily’ consisting of the miR-17, miR-19, miR-130, miR-93, miR-18, miR-455 and miR-210 seed families, which cotargets critical tumour suppressors via a central GUGC core motif. We subsequently define mutations in microRNA target sites using the AGO-CLIP microRNA target atlas and TCGA exome-sequencing data. These combined analyses identify pan-cancer oncogenic cotargeting of the phosphoinositide 3-kinase, TGFβ and p53 pathways by the miR-17-19-130 superfamily members. Nature Pub. Group 2013-11-13 /pmc/articles/PMC3868236/ /pubmed/24220575 http://dx.doi.org/10.1038/ncomms3730 Text en Copyright © 2013, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/ |
spellingShingle | Article Hamilton, Mark P. Rajapakshe, Kimal Hartig, Sean M. Reva, Boris McLellan, Michael D. Kandoth, Cyriac Ding, Li Zack, Travis I. Gunaratne, Preethi H. Wheeler, David A. Coarfa, Cristian McGuire, Sean E. Identification of a pan-cancer oncogenic microRNA superfamily anchored by a central core seed motif |
title | Identification of a pan-cancer oncogenic microRNA superfamily anchored by a central core seed motif |
title_full | Identification of a pan-cancer oncogenic microRNA superfamily anchored by a central core seed motif |
title_fullStr | Identification of a pan-cancer oncogenic microRNA superfamily anchored by a central core seed motif |
title_full_unstemmed | Identification of a pan-cancer oncogenic microRNA superfamily anchored by a central core seed motif |
title_short | Identification of a pan-cancer oncogenic microRNA superfamily anchored by a central core seed motif |
title_sort | identification of a pan-cancer oncogenic microrna superfamily anchored by a central core seed motif |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3868236/ https://www.ncbi.nlm.nih.gov/pubmed/24220575 http://dx.doi.org/10.1038/ncomms3730 |
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