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Complex impact of DNA methylation on transcriptional dysregulation across 22 human cancer types
Accumulating evidence has demonstrated that transcriptional regulation is affected by DNA methylation. Understanding the perturbation of DNA methylation-mediated regulation between transcriptional factors (TFs) and targets is crucial for human diseases. However, the global landscape of DNA methylati...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7049702/ https://www.ncbi.nlm.nih.gov/pubmed/32002550 http://dx.doi.org/10.1093/nar/gkaa041 |
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author | Wang, Zishan Yin, Jiaqi Zhou, Weiwei Bai, Jing Xie, Yunjin Xu, Kang Zheng, Xiangyi Xiao, Jun Zhou, Li Qi, Xiaolin Li, Yongsheng Li, Xia Xu, Juan |
author_facet | Wang, Zishan Yin, Jiaqi Zhou, Weiwei Bai, Jing Xie, Yunjin Xu, Kang Zheng, Xiangyi Xiao, Jun Zhou, Li Qi, Xiaolin Li, Yongsheng Li, Xia Xu, Juan |
author_sort | Wang, Zishan |
collection | PubMed |
description | Accumulating evidence has demonstrated that transcriptional regulation is affected by DNA methylation. Understanding the perturbation of DNA methylation-mediated regulation between transcriptional factors (TFs) and targets is crucial for human diseases. However, the global landscape of DNA methylation-mediated transcriptional dysregulation (DMTD) across cancers has not been portrayed. Here, we systematically identified DMTD by integrative analysis of transcriptome, methylome and regulatome across 22 human cancer types. Our results revealed that transcriptional regulation was affected by DNA methylation, involving hundreds of methylation-sensitive TFs (MethTFs). In addition, pan-cancer MethTFs, the regulatory activity of which is generally affected by DNA methylation across cancers, exhibit dominant functional characteristics and regulate several cancer hallmarks. Moreover, pan-cancer MethTFs were found to be affected by DNA methylation in a complex pattern. Finally, we investigated the cooperation among MethTFs and identified a network module that consisted of 43 MethTFs with prognostic potential. In summary, we systematically dissected the transcriptional dysregulation mediated by DNA methylation across cancer types, and our results provide a valuable resource for both epigenetic and transcriptional regulation communities. |
format | Online Article Text |
id | pubmed-7049702 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-70497022020-03-10 Complex impact of DNA methylation on transcriptional dysregulation across 22 human cancer types Wang, Zishan Yin, Jiaqi Zhou, Weiwei Bai, Jing Xie, Yunjin Xu, Kang Zheng, Xiangyi Xiao, Jun Zhou, Li Qi, Xiaolin Li, Yongsheng Li, Xia Xu, Juan Nucleic Acids Res Computational Biology Accumulating evidence has demonstrated that transcriptional regulation is affected by DNA methylation. Understanding the perturbation of DNA methylation-mediated regulation between transcriptional factors (TFs) and targets is crucial for human diseases. However, the global landscape of DNA methylation-mediated transcriptional dysregulation (DMTD) across cancers has not been portrayed. Here, we systematically identified DMTD by integrative analysis of transcriptome, methylome and regulatome across 22 human cancer types. Our results revealed that transcriptional regulation was affected by DNA methylation, involving hundreds of methylation-sensitive TFs (MethTFs). In addition, pan-cancer MethTFs, the regulatory activity of which is generally affected by DNA methylation across cancers, exhibit dominant functional characteristics and regulate several cancer hallmarks. Moreover, pan-cancer MethTFs were found to be affected by DNA methylation in a complex pattern. Finally, we investigated the cooperation among MethTFs and identified a network module that consisted of 43 MethTFs with prognostic potential. In summary, we systematically dissected the transcriptional dysregulation mediated by DNA methylation across cancer types, and our results provide a valuable resource for both epigenetic and transcriptional regulation communities. Oxford University Press 2020-03-18 2020-01-31 /pmc/articles/PMC7049702/ /pubmed/32002550 http://dx.doi.org/10.1093/nar/gkaa041 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Computational Biology Wang, Zishan Yin, Jiaqi Zhou, Weiwei Bai, Jing Xie, Yunjin Xu, Kang Zheng, Xiangyi Xiao, Jun Zhou, Li Qi, Xiaolin Li, Yongsheng Li, Xia Xu, Juan Complex impact of DNA methylation on transcriptional dysregulation across 22 human cancer types |
title | Complex impact of DNA methylation on transcriptional dysregulation across 22 human cancer types |
title_full | Complex impact of DNA methylation on transcriptional dysregulation across 22 human cancer types |
title_fullStr | Complex impact of DNA methylation on transcriptional dysregulation across 22 human cancer types |
title_full_unstemmed | Complex impact of DNA methylation on transcriptional dysregulation across 22 human cancer types |
title_short | Complex impact of DNA methylation on transcriptional dysregulation across 22 human cancer types |
title_sort | complex impact of dna methylation on transcriptional dysregulation across 22 human cancer types |
topic | Computational Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7049702/ https://www.ncbi.nlm.nih.gov/pubmed/32002550 http://dx.doi.org/10.1093/nar/gkaa041 |
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