About: DNA methylation-associated colonic mucosal immune and defense responses in treatment-naive pediatric ulcerative colitis     Goto   Sponge   NotDistinct   Permalink

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Description
  • Inflammatory bowel diseases (IBD) are emerging globally, indicating that environmental factors may be important in their pathogenesis. Colonic mucosal epigenetic changes, such as DNA methylation, can occur in response to the environment and have been implicated in IBD pathology. However, mucosal DNA methylation has not been examined in treatment-naive patients. We studied DNA methylation in untreated, left sided colonic biopsy specimens using the Infinium HumanMethylation450 BeadChip array. We analyzed 22 control (C) patients, 15 untreated Crohn's disease (CD) patients, and 9 untreated ulcerative colitis (UC) patients from two cohorts. Samples obtained at the time of clinical remission from two of the treatment-naive UC patients were also included into the analysis. UC-specific gene expression was interrogated in a subset of adjacent samples (5 C and 5 UC) using the Affymetrix GeneChip PrimeView Human Gene Expression Arrays. Only treatment-naive UC separated from control. One-hundred-and-20 genes with significant expression change in UC (>2-fold, P < 0.05) were associated with differentially methylated regions (DMRs). Epigenetically associated gene expression changes (including gene expression changes in the IFITM1, ITGB2, S100A9, SLPI, SAA1, and STAT3 genes) were linked to colonic mucosal immune and defense responses. These findings underscore the relationship between epigenetic changes and inflammation in pediatric treatment-naive UC and may have potential etiologic, diagnostic, and therapeutic relevance for IBD.
  • Inflammatory bowel diseases (IBD) are emerging globally, indicating that environmental factors may be important in their pathogenesis. Colonic mucosal epigenetic changes, such as DNA methylation, can occur in response to the environment and have been implicated in IBD pathology. However, mucosal DNA methylation has not been examined in treatment-naive patients. We studied DNA methylation in untreated, left sided colonic biopsy specimens using the Infinium HumanMethylation450 BeadChip array. We analyzed 22 control (C) patients, 15 untreated Crohn's disease (CD) patients, and 9 untreated ulcerative colitis (UC) patients from two cohorts. Samples obtained at the time of clinical remission from two of the treatment-naive UC patients were also included into the analysis. UC-specific gene expression was interrogated in a subset of adjacent samples (5 C and 5 UC) using the Affymetrix GeneChip PrimeView Human Gene Expression Arrays. Only treatment-naive UC separated from control. One-hundred-and-20 genes with significant expression change in UC (>2-fold, P < 0.05) were associated with differentially methylated regions (DMRs). Epigenetically associated gene expression changes (including gene expression changes in the IFITM1, ITGB2, S100A9, SLPI, SAA1, and STAT3 genes) were linked to colonic mucosal immune and defense responses. These findings underscore the relationship between epigenetic changes and inflammation in pediatric treatment-naive UC and may have potential etiologic, diagnostic, and therapeutic relevance for IBD. (en)
Title
  • DNA methylation-associated colonic mucosal immune and defense responses in treatment-naive pediatric ulcerative colitis
  • DNA methylation-associated colonic mucosal immune and defense responses in treatment-naive pediatric ulcerative colitis (en)
skos:prefLabel
  • DNA methylation-associated colonic mucosal immune and defense responses in treatment-naive pediatric ulcerative colitis
  • DNA methylation-associated colonic mucosal immune and defense responses in treatment-naive pediatric ulcerative colitis (en)
skos:notation
  • RIV/00216208:11130/14:10292957!RIV15-MSM-11130___
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • I
http://linked.open...iv/cisloPeriodika
  • 8
http://linked.open...vai/riv/dodaniDat
http://linked.open...aciTvurceVysledku
http://linked.open.../riv/druhVysledku
http://linked.open...iv/duvernostUdaju
http://linked.open...titaPredkladatele
http://linked.open...dnocenehoVysledku
  • 12003
http://linked.open...ai/riv/idVysledku
  • RIV/00216208:11130/14:10292957
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • DNA methylome; DNA expression; DNA methylation; epigenetics; treatment-naive; ulcerative colitis; Pediatric inflammatory bowel disease (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • US - Spojené státy americké
http://linked.open...ontrolniKodProRIV
  • [B6E48BCE2D13]
http://linked.open...i/riv/nazevZdroje
  • Epigenetics
http://linked.open...in/vavai/riv/obor
http://linked.open...ichTvurcuVysledku
http://linked.open...cetTvurcuVysledku
http://linked.open...UplatneniVysledku
http://linked.open...v/svazekPeriodika
  • 9
http://linked.open...iv/tvurceVysledku
  • Bronský, Jiří
  • Ferry, George D.
  • Frank, Eibe
  • Harris, R. Alan
  • Kaplan, Jess L.
  • Kellermayer, Richard
  • Mir, Sabina A. V.
  • Nagy-Szakal, Dorottya
  • Opekun, Antone
  • Szigeti, Reka
  • Winter, Harland
http://linked.open...ain/vavai/riv/wos
  • 000341360600008
issn
  • 1559-2294
number of pages
http://bibframe.org/vocab/doi
  • 10.4161/epi.29446
http://localhost/t...ganizacniJednotka
  • 11130
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