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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
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.
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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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