Author
Listed:
- Wei Cao
(Zhengzhou Central Hospital Affiliated Zhengzhou University)
- Hayan Lee
(School of Medicine)
- Wei Wu
(University of California San Francisco
University of California San Francisco)
- Aubhishek Zaman
(University of California San Francisco
University of California San Francisco)
- Sean McCorkle
(Brookhaven National Laboratory)
- Ming Yan
(Zhengzhou University)
- Justin Chen
(School of Medicine)
- Qinghe Xing
(Fudan University)
- Nasa Sinnott-Armstrong
(School of Medicine)
- Hongen Xu
(Zhengzhou University)
- M. Reza Sailani
(School of Medicine)
- Wenxue Tang
(Zhengzhou University)
- Yuanbo Cui
(Zhengzhou Central Hospital Affiliated Zhengzhou University)
- Jia liu
(Zhengzhou Central Hospital Affiliated Zhengzhou University)
- Hongyan Guan
(Zhengzhou Central Hospital Affiliated Zhengzhou University)
- Pengju Lv
(Zhengzhou Central Hospital Affiliated Zhengzhou University)
- Xiaoyan Sun
(Zhengzhou Central Hospital Affiliated Zhengzhou University)
- Lei Sun
(Zhengzhou Central Hospital Affiliated Zhengzhou University)
- Pengli Han
(Zhengzhou Central Hospital Affiliated Zhengzhou University)
- Yanan Lou
(Zhengzhou Central Hospital Affiliated Zhengzhou University)
- Jing Chang
(Jiangsu Mai Jian Biotechnology Development Company)
- Jinwu Wang
(Linzhou Cancer Hospital)
- Yuchi Gao
(Annoroad Gene Company)
- Jiancheng Guo
(Zhengzhou University)
- Gundolf Schenk
(University of California San Francisco)
- Alan Hunter Shain
(University of California San Francisco)
- Fred G. Biddle
(University of Calgary)
- Eric Collisson
(University of California San Francisco
University of California San Francisco)
- Michael Snyder
(School of Medicine)
- Trever G. Bivona
(University of California San Francisco
University of California San Francisco)
Abstract
Epigenetic landscapes can shape physiologic and disease phenotypes. We used integrative, high resolution multi-omics methods to delineate the methylome landscape and characterize the oncogenic drivers of esophageal squamous cell carcinoma (ESCC). We found 98% of CpGs are hypomethylated across the ESCC genome. Hypo-methylated regions are enriched in areas with heterochromatin binding markers (H3K9me3, H3K27me3), while hyper-methylated regions are enriched in polycomb repressive complex (EZH2/SUZ12) recognizing regions. Altered methylation in promoters, enhancers, and gene bodies, as well as in polycomb repressive complex occupancy and CTCF binding sites are associated with cancer-specific gene dysregulation. Epigenetic-mediated activation of non-canonical WNT/β-catenin/MMP signaling and a YY1/lncRNA ESCCAL-1/ribosomal protein network are uncovered and validated as potential novel ESCC driver alterations. This study advances our understanding of how epigenetic landscapes shape cancer pathogenesis and provides a resource for biomarker and target discovery.
Suggested Citation
Wei Cao & Hayan Lee & Wei Wu & Aubhishek Zaman & Sean McCorkle & Ming Yan & Justin Chen & Qinghe Xing & Nasa Sinnott-Armstrong & Hongen Xu & M. Reza Sailani & Wenxue Tang & Yuanbo Cui & Jia liu & Hong, 2020.
"Multi-faceted epigenetic dysregulation of gene expression promotes esophageal squamous cell carcinoma,"
Nature Communications, Nature, vol. 11(1), pages 1-19, December.
Handle:
RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-020-17227-z
DOI: 10.1038/s41467-020-17227-z
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