4.8 Article

Complex impact of DNA methylation on transcriptional dysregulation across 22 human cancer types

期刊

NUCLEIC ACIDS RESEARCH
卷 48, 期 5, 页码 2287-2302

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OXFORD UNIV PRESS
DOI: 10.1093/nar/gkaa041

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资金

  1. National Key R&D Program of China [2018YFC2000100]
  2. National Natural Science Foundation of China [61873075, 31871338, 31970646]
  3. Heilongjiang Touyan Innovation Team Program
  4. Natural Science Foundation for Distinguished Young Scholars of Heilongjiang Province [JQ2019C004]

向作者/读者索取更多资源

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, pancancer 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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