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Published in: Tumor Biology 11/2016

01-11-2016 | Original Article

Global methylation profiling to identify epigenetic signature of gallbladder cancer and gallstone disease

Authors: Preeti Sharma, Shushruta Bhunia, Satish S. Poojary, Dinesh S. Tekcham, Mustafa Ahmed Barbhuiya, Sanjiv Gupta, Braj Raj Shrivastav, Pramod Kumar Tiwari

Published in: Tumor Biology | Issue 11/2016

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Abstract

Promoter methylation in various tumor suppressor genes is reported to influence gallbladder carcinogenesis. Here, we aimed to identify methylation status in gallbladder cancer (GBC) by performing a comprehensive genome-wide DNA methylation profiling. The methylation status of 485,577 CpG sites were investigated using Illumina’s Infinium Human Methylation 450 BeadChip array in 24 tissues (eight each of tumor, adjacent non-tumor, and gallstone). About 33,443 differentially methylated sites (DMRs) were obtained in the whole human genome, of which 24,188 (72 %) were hypermethylated and 9255 (28 %) were hypomethylated. The data also revealed that majority of the DMRs are localized on the proximal promoter region [Transcription start sites (TSS200, TSS1500) and 5′ untranslated region (5′UTR)] and first exon. Exclusion of first exon detected a total of 10,123 (79 %) hypermethylated and 2703 (21 %) hypomethylated sites. Comparative analysis of the later with our differential proteomics data resulted in identification of 7 hypermethylated or down-regulated (e.g., FBN1, LPP, and SOD3) and 61 hypomethylated or up-regulated markers (e.g., HBE1, SNRPF, TPD52) for GBC. These genes could be further validated on the basis of their methylation/expression status in order to identify their utility to be used as biomarker/s for early diagnosis and management of GBC.
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Metadata
Title
Global methylation profiling to identify epigenetic signature of gallbladder cancer and gallstone disease
Authors
Preeti Sharma
Shushruta Bhunia
Satish S. Poojary
Dinesh S. Tekcham
Mustafa Ahmed Barbhuiya
Sanjiv Gupta
Braj Raj Shrivastav
Pramod Kumar Tiwari
Publication date
01-11-2016
Publisher
Springer Netherlands
Published in
Tumor Biology / Issue 11/2016
Print ISSN: 1010-4283
Electronic ISSN: 1423-0380
DOI
https://doi.org/10.1007/s13277-016-5355-9

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