Network Analysis of Common Genes and Transcriptional Factors between Celiac Disease and Inflammatory Bowel Diseases

BACKGROUND Understanding the associations among different disorders remarkably improves their diagnosis and treatments. Celiac disease is the most complicated and prevalent form of immune-mediated diseases. On the other hand, inflammatory bowel diseases lead to inflammation of the intestine with an...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Middle East journal of digestive diseases 2020-10, Vol.12 (4), p.257-264
Hauptverfasser: Izadi, Fereshteh, Soheilifar, Mohammad Hasan, Keshmiri Neghab, Hoda, Soheilifar, Mahya, Esmaeeli Djavid, Gholamreza
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 264
container_issue 4
container_start_page 257
container_title Middle East journal of digestive diseases
container_volume 12
creator Izadi, Fereshteh
Soheilifar, Mohammad Hasan
Keshmiri Neghab, Hoda
Soheilifar, Mahya
Esmaeeli Djavid, Gholamreza
description BACKGROUND Understanding the associations among different disorders remarkably improves their diagnosis and treatments. Celiac disease is the most complicated and prevalent form of immune-mediated diseases. On the other hand, inflammatory bowel diseases lead to inflammation of the intestine with an unknown cause. Although inflammatory bowel diseases have been often thought of as an autoimmune disorder, they can be triggered by whatever that can lead to the inflammation in the whole bowel. Henceforth, both aforementioned diseases are related to autoimmune attacks and cause a sort of inflammatory event, which exploring trade-off among them supposedly will lead to discovering important genes and, in turn, to the possible common therapeutic protocols. In the current study, we aimed to determine the correlation between the common genes in celiac disease and inflammatory bowel diseases. METHODS 314 and 851 genes correlated with celiac disease and inflammatory bowel diseases respectively extracted from DisGeNET were subjected to an in-silico data analysis framework to mine prognosticates genes and the associated pathways. RESULTS 149 shared genes between these diseases regulated by highlighted transcription factors NFKB1, IRF1, STAT1, HSF1, GATA3 were characterized as discriminating molecules, which by further screening were enriched in pathways mostly involved in apoptosis, T cell activation, and cytokine, chemokine, and interleukin signaling. CONCLUSION We observed that the identified common genes were associated with a wide range of pathogenic mechanisms underlying these diseases.
doi_str_mv 10.34172/mejdd.2020.191
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7859603</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2457730956</sourcerecordid><originalsourceid>FETCH-LOGICAL-p209t-8bdf483ea79e2e1b3fd202c1958df71dce51fa7d14d3e7979cb77123f0dd1c983</originalsourceid><addsrcrecordid>eNpdkU1PwzAMhiMEggl25oYiceGykY-2SS5IMGAgTXAZ5yptXMhok5F0oP17AgwE-GJLfvzqtY3QISVjnlHBTjtYGDNmhJExVXQLDRghcpSzTG3_1JzsoWGMC5KCq0KJbBftcZ4XGZd8gOId9G8-PONzp9t1tBH7Bk9813mHp-AgYu0MngftYh3ssrc-cfha170PEVdpGMDhCbRW1_jSRtARPkduXdPqrtOJW-ML_wbtdzseoJ1GtxGGm7yPHq6v5pOb0ex-ejs5n42WjKh-JCvTZJKDFgoY0Io3Jq1aU5VL0whqashpo4WhmeEglFB1JQRlvCHG0FpJvo_OvnSXq6qDxLs-6LZcBtvpsC69tuXfjrNP5aN_LYXMVUF4EjjZCAT_soLYl52NNbStduBXsWSZlLRQUhUJPf6HLvwqpFt9ULkQnKj8gzr67ejHyvc_-DsvtZB7</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2457730956</pqid></control><display><type>article</type><title>Network Analysis of Common Genes and Transcriptional Factors between Celiac Disease and Inflammatory Bowel Diseases</title><source>PubMed Central Open Access</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><creator>Izadi, Fereshteh ; Soheilifar, Mohammad Hasan ; Keshmiri Neghab, Hoda ; Soheilifar, Mahya ; Esmaeeli Djavid, Gholamreza</creator><creatorcontrib>Izadi, Fereshteh ; Soheilifar, Mohammad Hasan ; Keshmiri Neghab, Hoda ; Soheilifar, Mahya ; Esmaeeli Djavid, Gholamreza</creatorcontrib><description>BACKGROUND Understanding the associations among different disorders remarkably improves their diagnosis and treatments. Celiac disease is the most complicated and prevalent form of immune-mediated diseases. On the other hand, inflammatory bowel diseases lead to inflammation of the intestine with an unknown cause. Although inflammatory bowel diseases have been often thought of as an autoimmune disorder, they can be triggered by whatever that can lead to the inflammation in the whole bowel. Henceforth, both aforementioned diseases are related to autoimmune attacks and cause a sort of inflammatory event, which exploring trade-off among them supposedly will lead to discovering important genes and, in turn, to the possible common therapeutic protocols. In the current study, we aimed to determine the correlation between the common genes in celiac disease and inflammatory bowel diseases. METHODS 314 and 851 genes correlated with celiac disease and inflammatory bowel diseases respectively extracted from DisGeNET were subjected to an in-silico data analysis framework to mine prognosticates genes and the associated pathways. RESULTS 149 shared genes between these diseases regulated by highlighted transcription factors NFKB1, IRF1, STAT1, HSF1, GATA3 were characterized as discriminating molecules, which by further screening were enriched in pathways mostly involved in apoptosis, T cell activation, and cytokine, chemokine, and interleukin signaling. CONCLUSION We observed that the identified common genes were associated with a wide range of pathogenic mechanisms underlying these diseases.</description><identifier>ISSN: 2008-5230</identifier><identifier>EISSN: 2008-5249</identifier><identifier>DOI: 10.34172/mejdd.2020.191</identifier><identifier>PMID: 33564383</identifier><language>eng</language><publisher>Iran: Shiraz University of Medical Sciences</publisher><subject>Apoptosis ; Autoimmune diseases ; Celiac disease ; Cytokines ; Gene expression ; Gluten ; Immune system ; Inflammation ; Inflammatory bowel disease ; Investigations ; Irritable bowel syndrome ; Original ; Transcription factors</subject><ispartof>Middle East journal of digestive diseases, 2020-10, Vol.12 (4), p.257-264</ispartof><rights>2020 Middle East Journal of Digestive Diseases.</rights><rights>Copyright Shiraz University of Medical Sciences Oct 2020</rights><rights>2020 Middle East Journal of Digestive Diseases 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7859603/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7859603/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33564383$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Izadi, Fereshteh</creatorcontrib><creatorcontrib>Soheilifar, Mohammad Hasan</creatorcontrib><creatorcontrib>Keshmiri Neghab, Hoda</creatorcontrib><creatorcontrib>Soheilifar, Mahya</creatorcontrib><creatorcontrib>Esmaeeli Djavid, Gholamreza</creatorcontrib><title>Network Analysis of Common Genes and Transcriptional Factors between Celiac Disease and Inflammatory Bowel Diseases</title><title>Middle East journal of digestive diseases</title><addtitle>Middle East J Dig Dis</addtitle><description>BACKGROUND Understanding the associations among different disorders remarkably improves their diagnosis and treatments. Celiac disease is the most complicated and prevalent form of immune-mediated diseases. On the other hand, inflammatory bowel diseases lead to inflammation of the intestine with an unknown cause. Although inflammatory bowel diseases have been often thought of as an autoimmune disorder, they can be triggered by whatever that can lead to the inflammation in the whole bowel. Henceforth, both aforementioned diseases are related to autoimmune attacks and cause a sort of inflammatory event, which exploring trade-off among them supposedly will lead to discovering important genes and, in turn, to the possible common therapeutic protocols. In the current study, we aimed to determine the correlation between the common genes in celiac disease and inflammatory bowel diseases. METHODS 314 and 851 genes correlated with celiac disease and inflammatory bowel diseases respectively extracted from DisGeNET were subjected to an in-silico data analysis framework to mine prognosticates genes and the associated pathways. RESULTS 149 shared genes between these diseases regulated by highlighted transcription factors NFKB1, IRF1, STAT1, HSF1, GATA3 were characterized as discriminating molecules, which by further screening were enriched in pathways mostly involved in apoptosis, T cell activation, and cytokine, chemokine, and interleukin signaling. CONCLUSION We observed that the identified common genes were associated with a wide range of pathogenic mechanisms underlying these diseases.</description><subject>Apoptosis</subject><subject>Autoimmune diseases</subject><subject>Celiac disease</subject><subject>Cytokines</subject><subject>Gene expression</subject><subject>Gluten</subject><subject>Immune system</subject><subject>Inflammation</subject><subject>Inflammatory bowel disease</subject><subject>Investigations</subject><subject>Irritable bowel syndrome</subject><subject>Original</subject><subject>Transcription factors</subject><issn>2008-5230</issn><issn>2008-5249</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNpdkU1PwzAMhiMEggl25oYiceGykY-2SS5IMGAgTXAZ5yptXMhok5F0oP17AgwE-GJLfvzqtY3QISVjnlHBTjtYGDNmhJExVXQLDRghcpSzTG3_1JzsoWGMC5KCq0KJbBftcZ4XGZd8gOId9G8-PONzp9t1tBH7Bk9813mHp-AgYu0MngftYh3ssrc-cfha170PEVdpGMDhCbRW1_jSRtARPkduXdPqrtOJW-ML_wbtdzseoJ1GtxGGm7yPHq6v5pOb0ex-ejs5n42WjKh-JCvTZJKDFgoY0Io3Jq1aU5VL0whqashpo4WhmeEglFB1JQRlvCHG0FpJvo_OvnSXq6qDxLs-6LZcBtvpsC69tuXfjrNP5aN_LYXMVUF4EjjZCAT_soLYl52NNbStduBXsWSZlLRQUhUJPf6HLvwqpFt9ULkQnKj8gzr67ejHyvc_-DsvtZB7</recordid><startdate>20201001</startdate><enddate>20201001</enddate><creator>Izadi, Fereshteh</creator><creator>Soheilifar, Mohammad Hasan</creator><creator>Keshmiri Neghab, Hoda</creator><creator>Soheilifar, Mahya</creator><creator>Esmaeeli Djavid, Gholamreza</creator><general>Shiraz University of Medical Sciences</general><general>Iranian Association of Gastroerterology and Hepatology</general><scope>NPM</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>CWDGH</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20201001</creationdate><title>Network Analysis of Common Genes and Transcriptional Factors between Celiac Disease and Inflammatory Bowel Diseases</title><author>Izadi, Fereshteh ; Soheilifar, Mohammad Hasan ; Keshmiri Neghab, Hoda ; Soheilifar, Mahya ; Esmaeeli Djavid, Gholamreza</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p209t-8bdf483ea79e2e1b3fd202c1958df71dce51fa7d14d3e7979cb77123f0dd1c983</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Apoptosis</topic><topic>Autoimmune diseases</topic><topic>Celiac disease</topic><topic>Cytokines</topic><topic>Gene expression</topic><topic>Gluten</topic><topic>Immune system</topic><topic>Inflammation</topic><topic>Inflammatory bowel disease</topic><topic>Investigations</topic><topic>Irritable bowel syndrome</topic><topic>Original</topic><topic>Transcription factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Izadi, Fereshteh</creatorcontrib><creatorcontrib>Soheilifar, Mohammad Hasan</creatorcontrib><creatorcontrib>Keshmiri Neghab, Hoda</creatorcontrib><creatorcontrib>Soheilifar, Mahya</creatorcontrib><creatorcontrib>Esmaeeli Djavid, Gholamreza</creatorcontrib><collection>PubMed</collection><collection>ProQuest Central (Corporate)</collection><collection>Proquest Nursing &amp; Allied Health Source</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>British Nursing Database</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Middle East &amp; Africa Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Middle East journal of digestive diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Izadi, Fereshteh</au><au>Soheilifar, Mohammad Hasan</au><au>Keshmiri Neghab, Hoda</au><au>Soheilifar, Mahya</au><au>Esmaeeli Djavid, Gholamreza</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Network Analysis of Common Genes and Transcriptional Factors between Celiac Disease and Inflammatory Bowel Diseases</atitle><jtitle>Middle East journal of digestive diseases</jtitle><addtitle>Middle East J Dig Dis</addtitle><date>2020-10-01</date><risdate>2020</risdate><volume>12</volume><issue>4</issue><spage>257</spage><epage>264</epage><pages>257-264</pages><issn>2008-5230</issn><eissn>2008-5249</eissn><abstract>BACKGROUND Understanding the associations among different disorders remarkably improves their diagnosis and treatments. Celiac disease is the most complicated and prevalent form of immune-mediated diseases. On the other hand, inflammatory bowel diseases lead to inflammation of the intestine with an unknown cause. Although inflammatory bowel diseases have been often thought of as an autoimmune disorder, they can be triggered by whatever that can lead to the inflammation in the whole bowel. Henceforth, both aforementioned diseases are related to autoimmune attacks and cause a sort of inflammatory event, which exploring trade-off among them supposedly will lead to discovering important genes and, in turn, to the possible common therapeutic protocols. In the current study, we aimed to determine the correlation between the common genes in celiac disease and inflammatory bowel diseases. METHODS 314 and 851 genes correlated with celiac disease and inflammatory bowel diseases respectively extracted from DisGeNET were subjected to an in-silico data analysis framework to mine prognosticates genes and the associated pathways. RESULTS 149 shared genes between these diseases regulated by highlighted transcription factors NFKB1, IRF1, STAT1, HSF1, GATA3 were characterized as discriminating molecules, which by further screening were enriched in pathways mostly involved in apoptosis, T cell activation, and cytokine, chemokine, and interleukin signaling. CONCLUSION We observed that the identified common genes were associated with a wide range of pathogenic mechanisms underlying these diseases.</abstract><cop>Iran</cop><pub>Shiraz University of Medical Sciences</pub><pmid>33564383</pmid><doi>10.34172/mejdd.2020.191</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 2008-5230
ispartof Middle East journal of digestive diseases, 2020-10, Vol.12 (4), p.257-264
issn 2008-5230
2008-5249
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7859603
source PubMed Central Open Access; EZB-FREE-00999 freely available EZB journals; PubMed Central
subjects Apoptosis
Autoimmune diseases
Celiac disease
Cytokines
Gene expression
Gluten
Immune system
Inflammation
Inflammatory bowel disease
Investigations
Irritable bowel syndrome
Original
Transcription factors
title Network Analysis of Common Genes and Transcriptional Factors between Celiac Disease and Inflammatory Bowel Diseases
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-06T21%3A45%3A04IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Network%20Analysis%20of%20Common%20Genes%20and%20Transcriptional%20Factors%20between%20Celiac%20Disease%20and%20Inflammatory%20Bowel%20Diseases&rft.jtitle=Middle%20East%20journal%20of%20digestive%20diseases&rft.au=Izadi,%20Fereshteh&rft.date=2020-10-01&rft.volume=12&rft.issue=4&rft.spage=257&rft.epage=264&rft.pages=257-264&rft.issn=2008-5230&rft.eissn=2008-5249&rft_id=info:doi/10.34172/mejdd.2020.191&rft_dat=%3Cproquest_pubme%3E2457730956%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2457730956&rft_id=info:pmid/33564383&rfr_iscdi=true