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dc.contributor.authorHan, Qiyuan
dc.contributor.authorKono, Thomas JY
dc.contributor.authorKnutson, Charles G
dc.contributor.authorParry, Nicola M
dc.contributor.authorSeiler, Christopher L
dc.contributor.authorFox, James G
dc.contributor.authorTannenbaum, Steven R
dc.contributor.authorTretyakova, Natalia Y
dc.date.accessioned2021-10-27T19:53:43Z
dc.date.available2021-10-27T19:53:43Z
dc.date.issued2020
dc.identifier.urihttps://hdl.handle.net/1721.1/133596
dc.description.abstract© 2021 by the authors. Licensee MDPI, Basel, Switzerland. Epigenetic dysregulation is hypothesized to play a role in the observed association between inflammatory bowel disease (IBD) and colon tumor development. In the present work, DNA methylome, hydroxymethylome, and transcriptome analyses were conducted in proximal colon tissues harvested from the Helicobacter hepaticus (H. hepaticus)-infected murine model of IBD. Reduced representation bisulfite sequencing (RRBS) and oxidative RRBS (oxRRBS) analyses identified 1606 differentially methylated regions (DMR) and 3011 differentially hydroxymethylated regions (DhMR). These DMR/DhMR overlapped with genes that are associated with gastrointestinal disease, inflammatory disease, and cancer. RNA-seq revealed pronounced expression changes of a number of genes associated with inflammation and cancer. Several genes including Duox2, Tgm2, Cdhr5, and Hk2 exhibited changes in both DNA methylation/hydroxymethylation and gene expression levels. Overall, our results suggest that chronic inflammation triggers changes in methylation and hydroxymethylation patterns in the genome, altering the expression of key tumorigenesis genes and potentially contributing to the initiation of colorectal cancer.en_US
dc.language.isoen
dc.publisherMDPI AGen_US
dc.relation.isversionof10.3390/IJMS22010364en_US
dc.rightsCreative Commons Attribution 4.0 International licenseen_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.sourceMDPIen_US
dc.titleMulti-Omics Characterization of Inflammatory Bowel Disease-Induced Hyperplasia/Dysplasia in the Rag2−/−/Il10−/− Mouse Modelen_US
dc.typeArticleen_US
dc.relation.journalInternational Journal of Molecular Sciencesen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2021-09-10T14:46:46Z
dspace.orderedauthorsHan, Q; Kono, TJY; Knutson, CG; Parry, NM; Seiler, CL; Fox, JG; Tannenbaum, SR; Tretyakova, NYen_US
dspace.date.submission2021-09-10T14:46:48Z
mit.journal.volume22en_US
mit.journal.issue1en_US
mit.licensePUBLISHER_CC
mit.metadata.statusAuthority Work and Publication Information Neededen_US
mit.metadata.statusAuthority Work and Publication Information Needed


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