Hepatocellular carcinoma displays distinct DNA methylation signatures with potential as clinical predictors.

<h4>Background</h4>Hepatocellular carcinoma (HCC) is characterized by late detection and fast progression, and it is believed that epigenetic disruption may be the cause of its molecular and clinicopathological heterogeneity. A better understanding of the global deregulation of methylati...

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Main Authors: Hector Hernandez-Vargas, Marie-Pierre Lambert, Florence Le Calvez-Kelm, Géraldine Gouysse, Sandrine McKay-Chopin, Sean V Tavtigian, Jean-Yves Scoazec, Zdenko Herceg
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2010-03-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20305825/?tool=EBI
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author Hector Hernandez-Vargas
Marie-Pierre Lambert
Florence Le Calvez-Kelm
Géraldine Gouysse
Sandrine McKay-Chopin
Sean V Tavtigian
Jean-Yves Scoazec
Zdenko Herceg
author_facet Hector Hernandez-Vargas
Marie-Pierre Lambert
Florence Le Calvez-Kelm
Géraldine Gouysse
Sandrine McKay-Chopin
Sean V Tavtigian
Jean-Yves Scoazec
Zdenko Herceg
author_sort Hector Hernandez-Vargas
collection DOAJ
description <h4>Background</h4>Hepatocellular carcinoma (HCC) is characterized by late detection and fast progression, and it is believed that epigenetic disruption may be the cause of its molecular and clinicopathological heterogeneity. A better understanding of the global deregulation of methylation states and how they correlate with disease progression will aid in the design of strategies for earlier detection and better therapeutic decisions.<h4>Methods and findings</h4>We characterized the changes in promoter methylation in a series of 30 HCC tumors and their respective surrounding tissue and identified methylation signatures associated with major risk factors and clinical correlates. A wide panel of cancer-related gene promoters was analyzed using Illumina bead array technology, and CpG sites were then selected according to their ability to classify clinicopathological parameters. An independent series of HCC tumors and matched surrounding tissue was used for validation of the signatures. We were able to develop and validate a signature of methylation in HCC. This signature distinguished HCC from surrounding tissue and from other tumor types, and was independent of risk factors. However, aberrant methylation of an independent subset of promoters was associated with tumor progression and etiological risk factors (HBV or HCV infection and alcohol consumption). Interestingly, distinct methylation of an independent panel of gene promoters was strongly correlated with survival after cancer therapy.<h4>Conclusion</h4>Our study shows that HCC tumors exhibit specific DNA methylation signatures associated with major risk factors and tumor progression stage, with potential clinical applications in diagnosis and prognosis.
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spelling doaj.art-389baa5725c54169a07b5d9e17960c622022-12-21T23:09:40ZengPublic Library of Science (PLoS)PLoS ONE1932-62032010-03-0153e974910.1371/journal.pone.0009749Hepatocellular carcinoma displays distinct DNA methylation signatures with potential as clinical predictors.Hector Hernandez-VargasMarie-Pierre LambertFlorence Le Calvez-KelmGéraldine GouysseSandrine McKay-ChopinSean V TavtigianJean-Yves ScoazecZdenko Herceg<h4>Background</h4>Hepatocellular carcinoma (HCC) is characterized by late detection and fast progression, and it is believed that epigenetic disruption may be the cause of its molecular and clinicopathological heterogeneity. A better understanding of the global deregulation of methylation states and how they correlate with disease progression will aid in the design of strategies for earlier detection and better therapeutic decisions.<h4>Methods and findings</h4>We characterized the changes in promoter methylation in a series of 30 HCC tumors and their respective surrounding tissue and identified methylation signatures associated with major risk factors and clinical correlates. A wide panel of cancer-related gene promoters was analyzed using Illumina bead array technology, and CpG sites were then selected according to their ability to classify clinicopathological parameters. An independent series of HCC tumors and matched surrounding tissue was used for validation of the signatures. We were able to develop and validate a signature of methylation in HCC. This signature distinguished HCC from surrounding tissue and from other tumor types, and was independent of risk factors. However, aberrant methylation of an independent subset of promoters was associated with tumor progression and etiological risk factors (HBV or HCV infection and alcohol consumption). Interestingly, distinct methylation of an independent panel of gene promoters was strongly correlated with survival after cancer therapy.<h4>Conclusion</h4>Our study shows that HCC tumors exhibit specific DNA methylation signatures associated with major risk factors and tumor progression stage, with potential clinical applications in diagnosis and prognosis.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20305825/?tool=EBI
spellingShingle Hector Hernandez-Vargas
Marie-Pierre Lambert
Florence Le Calvez-Kelm
Géraldine Gouysse
Sandrine McKay-Chopin
Sean V Tavtigian
Jean-Yves Scoazec
Zdenko Herceg
Hepatocellular carcinoma displays distinct DNA methylation signatures with potential as clinical predictors.
PLoS ONE
title Hepatocellular carcinoma displays distinct DNA methylation signatures with potential as clinical predictors.
title_full Hepatocellular carcinoma displays distinct DNA methylation signatures with potential as clinical predictors.
title_fullStr Hepatocellular carcinoma displays distinct DNA methylation signatures with potential as clinical predictors.
title_full_unstemmed Hepatocellular carcinoma displays distinct DNA methylation signatures with potential as clinical predictors.
title_short Hepatocellular carcinoma displays distinct DNA methylation signatures with potential as clinical predictors.
title_sort hepatocellular carcinoma displays distinct dna methylation signatures with potential as clinical predictors
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20305825/?tool=EBI
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