Integrative analysis of DNA methylation and gene expression reveals hepatocellular carcinoma-specific diagnostic biomarkers

Abstract Background Hepatocellular carcinoma (HCC) is the one of the most common cancers and lethal diseases in the world. DNA methylation alteration is frequently observed in HCC and may play important roles in carcinogenesis and diagnosis. Methods Using the TCGA HCC dataset, we classified HCC pati...

Full description

Bibliographic Details
Main Authors: Jinming Cheng, Dongkai Wei, Yuan Ji, Lingli Chen, Liguang Yang, Guang Li, Leilei Wu, Ting Hou, Lu Xie, Guohui Ding, Hong Li, Yixue Li
Format: Article
Language:English
Published: BMC 2018-05-01
Series:Genome Medicine
Subjects:
Online Access:http://link.springer.com/article/10.1186/s13073-018-0548-z
_version_ 1818242704082993152
author Jinming Cheng
Dongkai Wei
Yuan Ji
Lingli Chen
Liguang Yang
Guang Li
Leilei Wu
Ting Hou
Lu Xie
Guohui Ding
Hong Li
Yixue Li
author_facet Jinming Cheng
Dongkai Wei
Yuan Ji
Lingli Chen
Liguang Yang
Guang Li
Leilei Wu
Ting Hou
Lu Xie
Guohui Ding
Hong Li
Yixue Li
author_sort Jinming Cheng
collection DOAJ
description Abstract Background Hepatocellular carcinoma (HCC) is the one of the most common cancers and lethal diseases in the world. DNA methylation alteration is frequently observed in HCC and may play important roles in carcinogenesis and diagnosis. Methods Using the TCGA HCC dataset, we classified HCC patients into different methylation subtypes, identified differentially methylated and expressed genes, and analyzed cis- and trans-regulation of DNA methylation and gene expression. To find potential diagnostic biomarkers for HCC, we screened HCC-specific CpGs by comparing the methylation profiles of 375 samples from HCC patients, 50 normal liver samples, 184 normal blood samples, and 3780 samples from patients with other cancers. A logistic regression model was constructed to distinguish HCC patients from normal controls. Model performance was evaluated using three independent datasets (including 327 HCC samples and 122 normal samples) and ten newly collected biopsies. Results We identified a group of patients with a CpG island methylator phenotype (CIMP) and found that the overall survival of CIMP patients was poorer than that of non-CIMP patients. Our analyses showed that the cis-regulation of DNA methylation and gene expression was dominated by the negative correlation, while the trans-regulation was more complex. More importantly, we identified six HCC-specific hypermethylated sites as potential diagnostic biomarkers. The combination of six sites achieved ~ 92% sensitivity in predicting HCC, ~ 98% specificity in excluding normal livers, and ~ 98% specificity in excluding other cancers. Compared with previously published methylation markers, our markers are the only ones that can distinguish HCC from other cancers. Conclusions Overall, our study systematically describes the DNA methylation characteristics of HCC and provides promising biomarkers for the diagnosis of HCC.
first_indexed 2024-12-12T13:49:27Z
format Article
id doaj.art-d5b2e3c7a4944d15adbad2e449b00955
institution Directory Open Access Journal
issn 1756-994X
language English
last_indexed 2024-12-12T13:49:27Z
publishDate 2018-05-01
publisher BMC
record_format Article
series Genome Medicine
spelling doaj.art-d5b2e3c7a4944d15adbad2e449b009552022-12-22T00:22:36ZengBMCGenome Medicine1756-994X2018-05-0110111110.1186/s13073-018-0548-zIntegrative analysis of DNA methylation and gene expression reveals hepatocellular carcinoma-specific diagnostic biomarkersJinming Cheng0Dongkai Wei1Yuan Ji2Lingli Chen3Liguang Yang4Guang Li5Leilei Wu6Ting Hou7Lu Xie8Guohui Ding9Hong Li10Yixue Li11Department of Bioinformatics and Biostatistics, School of Life Sciences and Biotechnology, Shanghai Jiao Tong UniversityBasepair biotechnology Co. LTDDepartment of Pathology, Zhongshan Hospital, Fudan UniversityDepartment of Pathology, Zhongshan Hospital, Fudan UniversityKey Lab of Computational Biology, CAS-MPG Partner Institute for Computational Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of SciencesBasepair biotechnology Co. LTDDepartment of Bioinformatics and Biostatistics, School of Life Sciences and Biotechnology, Shanghai Jiao Tong UniversityKey Lab of Computational Biology, CAS-MPG Partner Institute for Computational Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of SciencesShanghai Center for Bioinformation Technology, Shanghai Academy of Science and TechnologyKey Lab of Computational Biology, CAS-MPG Partner Institute for Computational Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of SciencesKey Lab of Computational Biology, CAS-MPG Partner Institute for Computational Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of SciencesDepartment of Bioinformatics and Biostatistics, School of Life Sciences and Biotechnology, Shanghai Jiao Tong UniversityAbstract Background Hepatocellular carcinoma (HCC) is the one of the most common cancers and lethal diseases in the world. DNA methylation alteration is frequently observed in HCC and may play important roles in carcinogenesis and diagnosis. Methods Using the TCGA HCC dataset, we classified HCC patients into different methylation subtypes, identified differentially methylated and expressed genes, and analyzed cis- and trans-regulation of DNA methylation and gene expression. To find potential diagnostic biomarkers for HCC, we screened HCC-specific CpGs by comparing the methylation profiles of 375 samples from HCC patients, 50 normal liver samples, 184 normal blood samples, and 3780 samples from patients with other cancers. A logistic regression model was constructed to distinguish HCC patients from normal controls. Model performance was evaluated using three independent datasets (including 327 HCC samples and 122 normal samples) and ten newly collected biopsies. Results We identified a group of patients with a CpG island methylator phenotype (CIMP) and found that the overall survival of CIMP patients was poorer than that of non-CIMP patients. Our analyses showed that the cis-regulation of DNA methylation and gene expression was dominated by the negative correlation, while the trans-regulation was more complex. More importantly, we identified six HCC-specific hypermethylated sites as potential diagnostic biomarkers. The combination of six sites achieved ~ 92% sensitivity in predicting HCC, ~ 98% specificity in excluding normal livers, and ~ 98% specificity in excluding other cancers. Compared with previously published methylation markers, our markers are the only ones that can distinguish HCC from other cancers. Conclusions Overall, our study systematically describes the DNA methylation characteristics of HCC and provides promising biomarkers for the diagnosis of HCC.http://link.springer.com/article/10.1186/s13073-018-0548-zHepatocellular carcinomaMethylationCpG island methylator phenotypeGene regulationSpecific diagnostic biomarker
spellingShingle Jinming Cheng
Dongkai Wei
Yuan Ji
Lingli Chen
Liguang Yang
Guang Li
Leilei Wu
Ting Hou
Lu Xie
Guohui Ding
Hong Li
Yixue Li
Integrative analysis of DNA methylation and gene expression reveals hepatocellular carcinoma-specific diagnostic biomarkers
Genome Medicine
Hepatocellular carcinoma
Methylation
CpG island methylator phenotype
Gene regulation
Specific diagnostic biomarker
title Integrative analysis of DNA methylation and gene expression reveals hepatocellular carcinoma-specific diagnostic biomarkers
title_full Integrative analysis of DNA methylation and gene expression reveals hepatocellular carcinoma-specific diagnostic biomarkers
title_fullStr Integrative analysis of DNA methylation and gene expression reveals hepatocellular carcinoma-specific diagnostic biomarkers
title_full_unstemmed Integrative analysis of DNA methylation and gene expression reveals hepatocellular carcinoma-specific diagnostic biomarkers
title_short Integrative analysis of DNA methylation and gene expression reveals hepatocellular carcinoma-specific diagnostic biomarkers
title_sort integrative analysis of dna methylation and gene expression reveals hepatocellular carcinoma specific diagnostic biomarkers
topic Hepatocellular carcinoma
Methylation
CpG island methylator phenotype
Gene regulation
Specific diagnostic biomarker
url http://link.springer.com/article/10.1186/s13073-018-0548-z
work_keys_str_mv AT jinmingcheng integrativeanalysisofdnamethylationandgeneexpressionrevealshepatocellularcarcinomaspecificdiagnosticbiomarkers
AT dongkaiwei integrativeanalysisofdnamethylationandgeneexpressionrevealshepatocellularcarcinomaspecificdiagnosticbiomarkers
AT yuanji integrativeanalysisofdnamethylationandgeneexpressionrevealshepatocellularcarcinomaspecificdiagnosticbiomarkers
AT linglichen integrativeanalysisofdnamethylationandgeneexpressionrevealshepatocellularcarcinomaspecificdiagnosticbiomarkers
AT liguangyang integrativeanalysisofdnamethylationandgeneexpressionrevealshepatocellularcarcinomaspecificdiagnosticbiomarkers
AT guangli integrativeanalysisofdnamethylationandgeneexpressionrevealshepatocellularcarcinomaspecificdiagnosticbiomarkers
AT leileiwu integrativeanalysisofdnamethylationandgeneexpressionrevealshepatocellularcarcinomaspecificdiagnosticbiomarkers
AT tinghou integrativeanalysisofdnamethylationandgeneexpressionrevealshepatocellularcarcinomaspecificdiagnosticbiomarkers
AT luxie integrativeanalysisofdnamethylationandgeneexpressionrevealshepatocellularcarcinomaspecificdiagnosticbiomarkers
AT guohuiding integrativeanalysisofdnamethylationandgeneexpressionrevealshepatocellularcarcinomaspecificdiagnosticbiomarkers
AT hongli integrativeanalysisofdnamethylationandgeneexpressionrevealshepatocellularcarcinomaspecificdiagnosticbiomarkers
AT yixueli integrativeanalysisofdnamethylationandgeneexpressionrevealshepatocellularcarcinomaspecificdiagnosticbiomarkers