Genome-Wide and Gene-Specific Epigenomic Platforms for Hepatocellular Carcinoma Biomarker Development Trials. (16th April 2014)
- Record Type:
- Journal Article
- Title:
- Genome-Wide and Gene-Specific Epigenomic Platforms for Hepatocellular Carcinoma Biomarker Development Trials. (16th April 2014)
- Main Title:
- Genome-Wide and Gene-Specific Epigenomic Platforms for Hepatocellular Carcinoma Biomarker Development Trials
- Authors:
- Michailidi, Christina
Soudry, Ethan
Brait, Mariana
Maldonado, Leonel
Jaffe, Andrew
Ili-Gangas, Carmen
Brebi-Mieville, Priscilla
Perez, Jimena
Kim, Myoung Sook
Zhong, Xiaoli
Yang, Quiang
Valle, Blanca
Meltzer, Stephen J.
Torbenson, Michael
Esteller, Manel
Sidransky, David
Guerrero-Preston, Rafael - Other Names:
- Zhao Ronghua Academic Editor.
- Abstract:
- Abstract : The majority of the epigenomic reports in hepatocellular carcinoma have focused on identifying novel differentially methylated drivers or passengers of the oncogenic process. Few reports have considered the technologies in place for clinical translation of newly identified biomarkers. The aim of this study was to identify epigenomic technologies that need only a small number of samples to discriminate HCC from non-HCC tissue, a basic requirement for biomarker development trials. To assess that potential, we used quantitative Methylation Specific PCR, oligonucleotide tiling arrays, and Methylation BeadChip assays. Concurrent global DNA hypomethylation, gene-specific hypermethylation, and chromatin alterations were observed as a hallmark of HCC. A global loss of promoter methylation was observed in HCC with the Illumina BeadChip assays and the Nimblegen oligonucleotide arrays. HCC samples had lower median methylation peak scores and a reduced number of significant promoter-wide methylated probes. Promoter hypermethylation of RASSF1A, SSBP2, and B4GALT1 quantified by qMSP had a sensitivity ranging from 38% to 52%, a specificity of 100%, and an AUC from 0.58 to 0.75. A panel combining these genes with HCC risk factors had a sensitivity of 87%, a specificity of 100%, and an AUC of 0.91.
- Is Part Of:
- Gastroenterology research and practice. Volume 2014(2014)
- Journal:
- Gastroenterology research and practice
- Issue:
- Volume 2014(2014)
- Issue Display:
- Volume 2014, Issue 2014 (2014)
- Year:
- 2014
- Volume:
- 2014
- Issue:
- 2014
- Issue Sort Value:
- 2014-2014-2014-0000
- Page Start:
- Page End:
- Publication Date:
- 2014-04-16
- Subjects:
- Gastroenterology -- Periodicals
Digestive organs -- Diseases -- Periodicals
616.33005 - Journal URLs:
- https://www.hindawi.com/journals/grp/ ↗
- DOI:
- 10.1155/2014/597164 ↗
- Languages:
- English
- ISSNs:
- 1687-6121
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library HMNTS - ELD Digital store
- Ingest File:
- 16853.xml