The effect of rebamipide on Helicobacter pylori extract‐mediated changes of gene expression in gastric epithelial cells
Summary Background : Recent studies have shown that Helicobacter pylori affects intracellular signal transduction in host cells, leading to the activation of transcriptional factors and the induction of pro‐inflammatory cytokines. On the other hand, rebamipide, an anti‐gastritis and anti‐ulcer agent...
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creator | Yoshida, N. Ishikawa, T. Ichiishi, E. Yoshida, Y. Hanashiro, K. Kuchide, M. Uchiyama, K. Kokura, S. Ichikawa, H. Naito, Y. Yamamura, Y. Okanoue, T. Yoshikawa, T. |
description | Summary
Background : Recent studies have shown that Helicobacter pylori affects intracellular signal transduction in host cells, leading to the activation of transcriptional factors and the induction of pro‐inflammatory cytokines. On the other hand, rebamipide, an anti‐gastritis and anti‐ulcer agent, could scavenge reactive oxygen species and reduce interleukin‐8 (IL‐8) expression in gastric epithelial cells induced by H. pylori‐stimulation through the attenuated activation of nuclear factor‐κB (NF‐κB).
Aims : In this study, we investigated the effects of rebamipide on gene expression in H. pylori‐stimulated epithelial cells using DNA chip.
Methods : H. pylori water extract (HPE) was prepared from NCTC11637, the type strain of H. pylori. Total RNA was extracted from MKN45 cells, a human gastric cancer cell line, following HPE‐stimulation with and without rebamipide for 3 h, and differences in gene expression profiles were observed using GeneChip and Human 6800 probe array.
Results : The GeneChip analysis demonstrated that 132 up‐regulated genes and 873 down‐regulated genes, such as growth factors, chemokines and transcription factors, were detected in MKN45 cells 3 h after stimulation of H. pylori. Among them, several genes, including bFGF, RANTES and MIP‐2β, were previously unknown to be expressed in H. pylori‐stimulated human gastric cells. Rebamipide reduced expression of 119 genes encoding cytokines, growth factors and their receptors and transcription factors.
Conclusions : These findings suggest that rebamipide could inhibit inflammatory reactions and tumour progression by modifying H. pylori infection‐induced gene expression in gastric epithelial cells. |
doi_str_mv | 10.1046/j.1365-2036.18.s1.7.x |
format | Article |
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Background : Recent studies have shown that Helicobacter pylori affects intracellular signal transduction in host cells, leading to the activation of transcriptional factors and the induction of pro‐inflammatory cytokines. On the other hand, rebamipide, an anti‐gastritis and anti‐ulcer agent, could scavenge reactive oxygen species and reduce interleukin‐8 (IL‐8) expression in gastric epithelial cells induced by H. pylori‐stimulation through the attenuated activation of nuclear factor‐κB (NF‐κB).
Aims : In this study, we investigated the effects of rebamipide on gene expression in H. pylori‐stimulated epithelial cells using DNA chip.
Methods : H. pylori water extract (HPE) was prepared from NCTC11637, the type strain of H. pylori. Total RNA was extracted from MKN45 cells, a human gastric cancer cell line, following HPE‐stimulation with and without rebamipide for 3 h, and differences in gene expression profiles were observed using GeneChip and Human 6800 probe array.
Results : The GeneChip analysis demonstrated that 132 up‐regulated genes and 873 down‐regulated genes, such as growth factors, chemokines and transcription factors, were detected in MKN45 cells 3 h after stimulation of H. pylori. Among them, several genes, including bFGF, RANTES and MIP‐2β, were previously unknown to be expressed in H. pylori‐stimulated human gastric cells. Rebamipide reduced expression of 119 genes encoding cytokines, growth factors and their receptors and transcription factors.
Conclusions : These findings suggest that rebamipide could inhibit inflammatory reactions and tumour progression by modifying H. pylori infection‐induced gene expression in gastric epithelial cells.</description><identifier>ISSN: 0269-2813</identifier><identifier>EISSN: 1365-2036</identifier><identifier>DOI: 10.1046/j.1365-2036.18.s1.7.x</identifier><identifier>PMID: 12925142</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Alanine - analogs & derivatives ; Alanine - pharmacology ; Anti-Ulcer Agents - pharmacology ; Biological and medical sciences ; Chemokine CCL5 - genetics ; Chemokine CXCL2 ; Digestive system ; Down-Regulation ; Epithelial Cells - metabolism ; Fibroblast Growth Factor 2 - genetics ; Gastric Mucosa - metabolism ; Gene Expression - drug effects ; Helicobacter pylori - drug effects ; Humans ; Medical sciences ; Monokines - metabolism ; NF-kappa B - metabolism ; Oligonucleotide Array Sequence Analysis ; Pharmacology. Drug treatments ; Quinolones - pharmacology ; Reverse Transcriptase Polymerase Chain Reaction ; RNA, Messenger - metabolism ; Stomach Neoplasms - metabolism ; Stomach Neoplasms - microbiology ; Tumor Cells, Cultured ; Up-Regulation</subject><ispartof>Alimentary pharmacology & therapeutics, 2003-07, Vol.18 (s1), p.63-75</ispartof><rights>2004 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4998-91cf9e1ea999f9b4c1fb4b1f0b736c316496958857d19a5533e0dd43e93e1e3a3</citedby><cites>FETCH-LOGICAL-c4998-91cf9e1ea999f9b4c1fb4b1f0b736c316496958857d19a5533e0dd43e93e1e3a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1046%2Fj.1365-2036.18.s1.7.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1046%2Fj.1365-2036.18.s1.7.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>309,310,314,780,784,789,790,1417,1433,23930,23931,25140,27924,27925,45574,45575,46409,46833</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=15043267$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12925142$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yoshida, N.</creatorcontrib><creatorcontrib>Ishikawa, T.</creatorcontrib><creatorcontrib>Ichiishi, E.</creatorcontrib><creatorcontrib>Yoshida, Y.</creatorcontrib><creatorcontrib>Hanashiro, K.</creatorcontrib><creatorcontrib>Kuchide, M.</creatorcontrib><creatorcontrib>Uchiyama, K.</creatorcontrib><creatorcontrib>Kokura, S.</creatorcontrib><creatorcontrib>Ichikawa, H.</creatorcontrib><creatorcontrib>Naito, Y.</creatorcontrib><creatorcontrib>Yamamura, Y.</creatorcontrib><creatorcontrib>Okanoue, T.</creatorcontrib><creatorcontrib>Yoshikawa, T.</creatorcontrib><title>The effect of rebamipide on Helicobacter pylori extract‐mediated changes of gene expression in gastric epithelial cells</title><title>Alimentary pharmacology & therapeutics</title><addtitle>Aliment Pharmacol Ther</addtitle><description>Summary
Background : Recent studies have shown that Helicobacter pylori affects intracellular signal transduction in host cells, leading to the activation of transcriptional factors and the induction of pro‐inflammatory cytokines. On the other hand, rebamipide, an anti‐gastritis and anti‐ulcer agent, could scavenge reactive oxygen species and reduce interleukin‐8 (IL‐8) expression in gastric epithelial cells induced by H. pylori‐stimulation through the attenuated activation of nuclear factor‐κB (NF‐κB).
Aims : In this study, we investigated the effects of rebamipide on gene expression in H. pylori‐stimulated epithelial cells using DNA chip.
Methods : H. pylori water extract (HPE) was prepared from NCTC11637, the type strain of H. pylori. Total RNA was extracted from MKN45 cells, a human gastric cancer cell line, following HPE‐stimulation with and without rebamipide for 3 h, and differences in gene expression profiles were observed using GeneChip and Human 6800 probe array.
Results : The GeneChip analysis demonstrated that 132 up‐regulated genes and 873 down‐regulated genes, such as growth factors, chemokines and transcription factors, were detected in MKN45 cells 3 h after stimulation of H. pylori. Among them, several genes, including bFGF, RANTES and MIP‐2β, were previously unknown to be expressed in H. pylori‐stimulated human gastric cells. Rebamipide reduced expression of 119 genes encoding cytokines, growth factors and their receptors and transcription factors.
Conclusions : These findings suggest that rebamipide could inhibit inflammatory reactions and tumour progression by modifying H. pylori infection‐induced gene expression in gastric epithelial cells.</description><subject>Alanine - analogs & derivatives</subject><subject>Alanine - pharmacology</subject><subject>Anti-Ulcer Agents - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Chemokine CCL5 - genetics</subject><subject>Chemokine CXCL2</subject><subject>Digestive system</subject><subject>Down-Regulation</subject><subject>Epithelial Cells - metabolism</subject><subject>Fibroblast Growth Factor 2 - genetics</subject><subject>Gastric Mucosa - metabolism</subject><subject>Gene Expression - drug effects</subject><subject>Helicobacter pylori - drug effects</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Monokines - metabolism</subject><subject>NF-kappa B - metabolism</subject><subject>Oligonucleotide Array Sequence Analysis</subject><subject>Pharmacology. Drug treatments</subject><subject>Quinolones - pharmacology</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>RNA, Messenger - metabolism</subject><subject>Stomach Neoplasms - metabolism</subject><subject>Stomach Neoplasms - microbiology</subject><subject>Tumor Cells, Cultured</subject><subject>Up-Regulation</subject><issn>0269-2813</issn><issn>1365-2036</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkMGO0zAQhi0EomXhEUC-wC3BE8dOzG1V7bJIK8GhnC3HGbeu0iTYqba98Qg8I0-yjlrRK6eRRt__z-gj5D2wHFgpP-9y4FJkBeMyhzqPkFf58QVZ_tu-JEtWSJUVNfAFeRPjjjEmK1a8JgsoVCGgLJbktN4iRefQTnRwNGBj9n70LdKhpw_YeTs0xk4Y6HjqhuApHqeQFn9__9lj682ELbVb028wzvkN9qnuOAaM0acG39ONiVPwluLop20qNB212HXxLXnlTBfx3WXekJ_3d-vVQ_b4_eu31e1jZkul6kyBdQoBjVLKqaa04JqyAceaikvLQZZKKlHXompBGSE4R9a2JUfFU4obfkM-nXvHMPw6YJz03sf5A9PjcIi64qICpXgCxRm0YYgxoNNj8HsTThqYnp3rnZ7t6tmuhlpH0JU-ptyHy4FDk5xcUxfJCfh4AUy0pnPB9NbHKydYyQtZJe7LmXvyHZ7-77q-_bFOBTV_Btcjn7E</recordid><startdate>200307</startdate><enddate>200307</enddate><creator>Yoshida, N.</creator><creator>Ishikawa, T.</creator><creator>Ichiishi, E.</creator><creator>Yoshida, Y.</creator><creator>Hanashiro, K.</creator><creator>Kuchide, M.</creator><creator>Uchiyama, K.</creator><creator>Kokura, S.</creator><creator>Ichikawa, H.</creator><creator>Naito, Y.</creator><creator>Yamamura, Y.</creator><creator>Okanoue, T.</creator><creator>Yoshikawa, T.</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>200307</creationdate><title>The effect of rebamipide on Helicobacter pylori extract‐mediated changes of gene expression in gastric epithelial cells</title><author>Yoshida, N. ; Ishikawa, T. ; Ichiishi, E. ; Yoshida, Y. ; Hanashiro, K. ; Kuchide, M. ; Uchiyama, K. ; Kokura, S. ; Ichikawa, H. ; Naito, Y. ; Yamamura, Y. ; Okanoue, T. ; Yoshikawa, T.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4998-91cf9e1ea999f9b4c1fb4b1f0b736c316496958857d19a5533e0dd43e93e1e3a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Alanine - analogs & derivatives</topic><topic>Alanine - pharmacology</topic><topic>Anti-Ulcer Agents - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Chemokine CCL5 - genetics</topic><topic>Chemokine CXCL2</topic><topic>Digestive system</topic><topic>Down-Regulation</topic><topic>Epithelial Cells - metabolism</topic><topic>Fibroblast Growth Factor 2 - genetics</topic><topic>Gastric Mucosa - metabolism</topic><topic>Gene Expression - drug effects</topic><topic>Helicobacter pylori - drug effects</topic><topic>Humans</topic><topic>Medical sciences</topic><topic>Monokines - metabolism</topic><topic>NF-kappa B - metabolism</topic><topic>Oligonucleotide Array Sequence Analysis</topic><topic>Pharmacology. Drug treatments</topic><topic>Quinolones - pharmacology</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>RNA, Messenger - metabolism</topic><topic>Stomach Neoplasms - metabolism</topic><topic>Stomach Neoplasms - microbiology</topic><topic>Tumor Cells, Cultured</topic><topic>Up-Regulation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yoshida, N.</creatorcontrib><creatorcontrib>Ishikawa, T.</creatorcontrib><creatorcontrib>Ichiishi, E.</creatorcontrib><creatorcontrib>Yoshida, Y.</creatorcontrib><creatorcontrib>Hanashiro, K.</creatorcontrib><creatorcontrib>Kuchide, M.</creatorcontrib><creatorcontrib>Uchiyama, K.</creatorcontrib><creatorcontrib>Kokura, S.</creatorcontrib><creatorcontrib>Ichikawa, H.</creatorcontrib><creatorcontrib>Naito, Y.</creatorcontrib><creatorcontrib>Yamamura, Y.</creatorcontrib><creatorcontrib>Okanoue, T.</creatorcontrib><creatorcontrib>Yoshikawa, T.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Alimentary pharmacology & therapeutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yoshida, N.</au><au>Ishikawa, T.</au><au>Ichiishi, E.</au><au>Yoshida, Y.</au><au>Hanashiro, K.</au><au>Kuchide, M.</au><au>Uchiyama, K.</au><au>Kokura, S.</au><au>Ichikawa, H.</au><au>Naito, Y.</au><au>Yamamura, Y.</au><au>Okanoue, T.</au><au>Yoshikawa, T.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The effect of rebamipide on Helicobacter pylori extract‐mediated changes of gene expression in gastric epithelial cells</atitle><jtitle>Alimentary pharmacology & therapeutics</jtitle><addtitle>Aliment Pharmacol Ther</addtitle><date>2003-07</date><risdate>2003</risdate><volume>18</volume><issue>s1</issue><spage>63</spage><epage>75</epage><pages>63-75</pages><issn>0269-2813</issn><eissn>1365-2036</eissn><abstract>Summary
Background : Recent studies have shown that Helicobacter pylori affects intracellular signal transduction in host cells, leading to the activation of transcriptional factors and the induction of pro‐inflammatory cytokines. On the other hand, rebamipide, an anti‐gastritis and anti‐ulcer agent, could scavenge reactive oxygen species and reduce interleukin‐8 (IL‐8) expression in gastric epithelial cells induced by H. pylori‐stimulation through the attenuated activation of nuclear factor‐κB (NF‐κB).
Aims : In this study, we investigated the effects of rebamipide on gene expression in H. pylori‐stimulated epithelial cells using DNA chip.
Methods : H. pylori water extract (HPE) was prepared from NCTC11637, the type strain of H. pylori. Total RNA was extracted from MKN45 cells, a human gastric cancer cell line, following HPE‐stimulation with and without rebamipide for 3 h, and differences in gene expression profiles were observed using GeneChip and Human 6800 probe array.
Results : The GeneChip analysis demonstrated that 132 up‐regulated genes and 873 down‐regulated genes, such as growth factors, chemokines and transcription factors, were detected in MKN45 cells 3 h after stimulation of H. pylori. Among them, several genes, including bFGF, RANTES and MIP‐2β, were previously unknown to be expressed in H. pylori‐stimulated human gastric cells. Rebamipide reduced expression of 119 genes encoding cytokines, growth factors and their receptors and transcription factors.
Conclusions : These findings suggest that rebamipide could inhibit inflammatory reactions and tumour progression by modifying H. pylori infection‐induced gene expression in gastric epithelial cells.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>12925142</pmid><doi>10.1046/j.1365-2036.18.s1.7.x</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Alanine - analogs & derivatives Alanine - pharmacology Anti-Ulcer Agents - pharmacology Biological and medical sciences Chemokine CCL5 - genetics Chemokine CXCL2 Digestive system Down-Regulation Epithelial Cells - metabolism Fibroblast Growth Factor 2 - genetics Gastric Mucosa - metabolism Gene Expression - drug effects Helicobacter pylori - drug effects Humans Medical sciences Monokines - metabolism NF-kappa B - metabolism Oligonucleotide Array Sequence Analysis Pharmacology. Drug treatments Quinolones - pharmacology Reverse Transcriptase Polymerase Chain Reaction RNA, Messenger - metabolism Stomach Neoplasms - metabolism Stomach Neoplasms - microbiology Tumor Cells, Cultured Up-Regulation |
title | The effect of rebamipide on Helicobacter pylori extract‐mediated changes of gene expression in gastric epithelial cells |
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