Abstract

Hepatocellular carcinoma harbors numerous genomic and epigenomic aberrations of DNA copy numbers and DNA methylation. Transcriptomic deregulation by these aberrations plays key driver roles in heterogeneous progression of cancers. Here, we profile DNA copy numbers, DNA methylation, and messenger RNA expression levels from 64 cases of hepatocellular carcinoma specimens. We find that the frequencies of the aberrancies of the DNA copy-number-correlated (CNVcor) expression genes and the methylation-correlated expression (METcor) genes are co-regulated significantly. Multi-omics integration of the CNVcor and METcor genes reveal three prognostic subtypes of hepatocellular carcinoma, which can be validated by an independent data. The most aggressive subtype expressing stemness genes has frequent BAP1 mutations, implying its pivotal role in the aggressive tumor progression. In conclusion, our integrative analysis of genomic and epigenomic regulation provides new insights on the multi-layered pathobiology of hepatocellular carcinoma, which might be helpful in developing precision management for hepatocellular carcinoma patients.

Details

Title
Integrative analysis of genomic and epigenomic regulation of the transcriptome in liver cancer
Author
Hyun Goo Woo 1   VIAFID ORCID Logo  ; Ji-Hye Choi 1 ; Yoon, Sarah 2 ; Jee, Byul A 1 ; Cho, Eun Ju 3 ; Jeong-Hoon, Lee 3   VIAFID ORCID Logo  ; Su Jong Yu 3 ; Jung-Hwan, Yoon 3 ; Nam-Joon, Yi 4 ; Kwang-Woong, Lee 4 ; Kyung-Suk Suh 4 ; Yoon Jun Kim 3 

 Department of Physiology, Ajou University School of Medicine, Suwon, Republic of Korea; Department of Biomedical Sciences, Graduate School, Ajou University, Suwon, Republic of Korea 
 Department of Physiology, Ajou University School of Medicine, Suwon, Republic of Korea 
 Department of Internal Medicine, Liver Research Institute, Seoul National University College of Medicine, Seoul, Republic of Korea 
 Department of Surgery, Seoul National University College of Medicine, Seoul, Republic of Korea 
Pages
1-11
Publication year
2017
Publication date
Oct 2017
Publisher
Nature Publishing Group
e-ISSN
20411723
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
1949581564
Copyright
© 2017. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.