Abstract

BackgroundWhile hepatitis B and C viral infection have been suppressed, non-B non-C hepatocellular carcinoma (NBNC-HCC) is considered to be rising in incidence terms in some developed countries where prevalence of those viral infections among HCC patients had been very high (such as Japan, Korea, and Italy). To elucidate critical molecular changes in NBNC-HCC, we integrated three large datasets relating to comprehensive array-based analysis of genome-wide DNA methylation (N = 43 pairs) and mRNA/miRNA expression (N = 15, and 24 pairs, respectively) via statistical modeling.ResultsHierarchical clustering of DNA methylation in miRNA coding regions clearly distinguished NBNC-HCC tissue samples from relevant background tissues, revealing a remarkable tumor-specific hypomethylation cluster. In addition, miRNA clusters were extremely hypomethylated in tumor samples (median methylation change for non-clustered miRNAs: -2.3%, clustered miRNAs: -24.6%). The proportion of CpGs hypomethylated in more than 90% of the samples was 55.9% of all CpGs within miRNA clusters, and the peak methylation level was drastically shifted from 84% to 39%. Following statistical adjustment, the difference in methylation levels within miRNA coding regions was positively associated with their expression change. Receiver operating characteristic (ROC) analysis revealed a great discriminatory ability in respect to cluster-miRNA methylation. Moreover, miRNA methylation change was negatively correlated with corresponding target gene expression amongst conserved and highly matched miRNA sites.ConclusionsWe observed a drastic negative shift of methylation levels in miRNA cluster regions. Changes in methylation status of miRNAs were more indicative of target gene expression and pathological diagnosis than respective miRNA expression changes, suggesting the importance of genome-wide miRNA methylation for tumor development. Our study dynamically summarized global miRNA hypomethylation and its genome-wide scale consequence in NBNC-HCC.Electronic supplementary materialThe online version of this article (doi:10.1186/s12943-016-0514-6) contains supplementary material, which is available to authorized users.

Highlights

  • While hepatitis B and C viral infection have been suppressed, non-B non-C hepatocellular carcinoma (NBNC-Hepatocellular carcinoma (HCC)) is considered to be rising in incidence terms in some developed countries where prevalence of those viral infections among HCC patients had been very high

  • While hepatitis B virus (HBV) and C virus (HCV) infection have been suppressed with development of public health measures and medical treatment, non-B non-C hepatocellular carcinoma (NBNC-HCC) is rising in incidence terms in Japan [2,3,4]

  • Differences in methylome state between NBNC-HCC tumor tissues and non-tumor background tissues Tissues from a total of 43 patients were used for this study, including 13 (30.2%) females and 30 (69.8%) males

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Summary

Introduction

While hepatitis B and C viral infection have been suppressed, non-B non-C hepatocellular carcinoma (NBNC-HCC) is considered to be rising in incidence terms in some developed countries where prevalence of those viral infections among HCC patients had been very high (such as Japan, Korea, and Italy). In terms of molecular oncology, altered epigenetic regulation is known to be an important contributory factor in tumor development. Epigenetic marks such as DNA methylation patterns are observed to be significantly different between cancer and non-cancer tissues, and a number of studies have indicated various cancerspecific epigenetic characteristics for every cancer type [6, 7]. Whether there are external “epimutagens” in other tumors including NBNC-HCC is an important research question

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