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

Author:

Wang Zishan1,Yin Jiaqi1,Zhou Weiwei1,Bai Jing1,Xie Yunjin1,Xu Kang1,Zheng Xiangyi1,Xiao Jun1,Zhou Li2,Qi Xiaolin3,Li Yongsheng134ORCID,Li Xia134ORCID,Xu Juan134

Affiliation:

1. College of Bioinformatics Science and Technology, Harbin Medical University, Harbin, China

2. Department of Nephrology, Affiliated Hospital of Chengde Medical College, Chengde, Hebei Province, China

3. Key Laboratory of Tropical Translational Medicine of Ministry of Education, Hainan Medical University, Haikou, Hainan 571199, China

4. College of Biomedical Information and Engineering, Hainan Medical University, Haikou, Hainan 570100, China

Abstract

Abstract 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.

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

Heilongjiang Touyan Innovation Team Program

Natural Science Foundation for Distinguished Young Scholars of Heilongjiang Province

Publisher

Oxford University Press (OUP)

Subject

Genetics

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