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Decreased Expression of Epidermal Growth Factor Receptor and mRNA of Its Ligands in Helicobacter pylori-infected Gastric Mucosa
Epidermal growth factor (EGF) and TGF-alpha play a central role in maintaining gastric mucosal integrity. Little is known about the regulative role of the four other widely expressed epidermal growth factor receptor ligands, heparin-binding EGF, amphiregulin, betacellulin and cripto in the gastric m...
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Published in: | Scandinavian journal of gastroenterology 2001, Vol.36 (1), p.23-31 |
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container_title | Scandinavian journal of gastroenterology |
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creator | SCHIEMANN, U KONTUREK, J. W OSTERHOFF, M ASSERT, R REMBIASZ, K PFEIFFER, D SCHATZ, H DOMSCHKE, W PFEIFFER, A |
description | Epidermal growth factor (EGF) and TGF-alpha play a central role in maintaining gastric mucosal integrity. Little is known about the regulative role of the four other widely expressed epidermal growth factor receptor ligands, heparin-binding EGF, amphiregulin, betacellulin and cripto in the gastric mucosa.
Nineteen patients with Helicobacter pylori-positive gastritis and 32 healthy controls were investigated. Mucosal mRNA expression of EGF receptor ligands was determined by quantitative PCR before and after H. pylori eradication. PCR products were analyzed by soft laser scanning densitometry. Moreover, the effect of chronic active gastritis on EGF receptor expression was assessed by [125I] EGF receptor autoradiography. Immunohistochemistry was performed for TGF-alpha to localize growth factor expression.
Antral and oxyntic biopsies showed strong mRNA expressions for TGF-alpha, amphiregulin and heparin binding EGF, but not for EGF, cripto and betacellulin. mRNA expression was significantly reduced down to 50% in H. pylori infection, significantly lower compared to normal gastric mucosa, and increased after eradication therapy. Moreover, chronic gastritis was associated with decreased antral EGF receptor binding compared to healthy controls, possibly reflecting reduced autoinduction. Immunohistochemical analyses localized TGF-alpha in the cytoplasma of gastric epithelial cells and revealed its increased expression after H. pylori eradication.
The data presented suggest that amphiregulin, heparin binding EGF and TGF-alpha are important EGF receptor ligands in the gastric mucosa. H. pylori infection apparently suppresses their mRNA as well as receptor expression that is reversed by H. pylori eradication. This deficiency of the gastroprotective EGF system may contribute to the gastric pathogenicity of H. pylori infection. |
doi_str_mv | 10.1080/00365520120960 |
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Nineteen patients with Helicobacter pylori-positive gastritis and 32 healthy controls were investigated. Mucosal mRNA expression of EGF receptor ligands was determined by quantitative PCR before and after H. pylori eradication. PCR products were analyzed by soft laser scanning densitometry. Moreover, the effect of chronic active gastritis on EGF receptor expression was assessed by [125I] EGF receptor autoradiography. Immunohistochemistry was performed for TGF-alpha to localize growth factor expression.
Antral and oxyntic biopsies showed strong mRNA expressions for TGF-alpha, amphiregulin and heparin binding EGF, but not for EGF, cripto and betacellulin. mRNA expression was significantly reduced down to 50% in H. pylori infection, significantly lower compared to normal gastric mucosa, and increased after eradication therapy. Moreover, chronic gastritis was associated with decreased antral EGF receptor binding compared to healthy controls, possibly reflecting reduced autoinduction. Immunohistochemical analyses localized TGF-alpha in the cytoplasma of gastric epithelial cells and revealed its increased expression after H. pylori eradication.
The data presented suggest that amphiregulin, heparin binding EGF and TGF-alpha are important EGF receptor ligands in the gastric mucosa. H. pylori infection apparently suppresses their mRNA as well as receptor expression that is reversed by H. pylori eradication. This deficiency of the gastroprotective EGF system may contribute to the gastric pathogenicity of H. pylori infection.</description><identifier>ISSN: 0036-5521</identifier><identifier>EISSN: 1502-7708</identifier><identifier>DOI: 10.1080/00365520120960</identifier><identifier>PMID: 11218236</identifier><identifier>CODEN: SJGRA4</identifier><language>eng</language><publisher>Copenhagen: Informa UK Ltd</publisher><subject>Adult ; Amphiregulin ; Bacterial diseases ; Bacterial diseases of the digestive system and abdomen ; Betacellulin ; Biological and medical sciences ; EGF Family of Proteins ; Epidermal Growth Factor - biosynthesis ; Epidermal Growth Factor Epidermal Growth Factor Receptor Ligands Helicobacter Pylori ; ErbB Receptors - biosynthesis ; Female ; Gastric Mucosa - metabolism ; Gastric Mucosa - microbiology ; Gastritis - metabolism ; Gastritis - microbiology ; Glycoproteins - biosynthesis ; GPI-Linked Proteins ; Growth Substances - biosynthesis ; Helicobacter Infections - metabolism ; Helicobacter pylori ; Heparin-binding EGF-like Growth Factor ; Human bacterial diseases ; Humans ; Infectious diseases ; Intercellular Signaling Peptides and Proteins ; Male ; Medical sciences ; Membrane Glycoproteins ; Neoplasm Proteins - biosynthesis ; Reverse Transcriptase Polymerase Chain Reaction ; RNA, Messenger - genetics ; Transforming Growth Factor alpha - biosynthesis</subject><ispartof>Scandinavian journal of gastroenterology, 2001, Vol.36 (1), p.23-31</ispartof><rights>2001 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 2001</rights><rights>2001 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2656-cf5b99c15ee0c49dcde3b5b6fba42297c934734a865ae260aa9019d30e9632093</citedby><cites>FETCH-LOGICAL-c2656-cf5b99c15ee0c49dcde3b5b6fba42297c934734a865ae260aa9019d30e9632093</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=884829$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11218236$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>SCHIEMANN, U</creatorcontrib><creatorcontrib>KONTUREK, J. W</creatorcontrib><creatorcontrib>OSTERHOFF, M</creatorcontrib><creatorcontrib>ASSERT, R</creatorcontrib><creatorcontrib>REMBIASZ, K</creatorcontrib><creatorcontrib>PFEIFFER, D</creatorcontrib><creatorcontrib>SCHATZ, H</creatorcontrib><creatorcontrib>DOMSCHKE, W</creatorcontrib><creatorcontrib>PFEIFFER, A</creatorcontrib><title>Decreased Expression of Epidermal Growth Factor Receptor and mRNA of Its Ligands in Helicobacter pylori-infected Gastric Mucosa</title><title>Scandinavian journal of gastroenterology</title><addtitle>Scand J Gastroenterol</addtitle><description>Epidermal growth factor (EGF) and TGF-alpha play a central role in maintaining gastric mucosal integrity. Little is known about the regulative role of the four other widely expressed epidermal growth factor receptor ligands, heparin-binding EGF, amphiregulin, betacellulin and cripto in the gastric mucosa.
Nineteen patients with Helicobacter pylori-positive gastritis and 32 healthy controls were investigated. Mucosal mRNA expression of EGF receptor ligands was determined by quantitative PCR before and after H. pylori eradication. PCR products were analyzed by soft laser scanning densitometry. Moreover, the effect of chronic active gastritis on EGF receptor expression was assessed by [125I] EGF receptor autoradiography. Immunohistochemistry was performed for TGF-alpha to localize growth factor expression.
Antral and oxyntic biopsies showed strong mRNA expressions for TGF-alpha, amphiregulin and heparin binding EGF, but not for EGF, cripto and betacellulin. mRNA expression was significantly reduced down to 50% in H. pylori infection, significantly lower compared to normal gastric mucosa, and increased after eradication therapy. Moreover, chronic gastritis was associated with decreased antral EGF receptor binding compared to healthy controls, possibly reflecting reduced autoinduction. Immunohistochemical analyses localized TGF-alpha in the cytoplasma of gastric epithelial cells and revealed its increased expression after H. pylori eradication.
The data presented suggest that amphiregulin, heparin binding EGF and TGF-alpha are important EGF receptor ligands in the gastric mucosa. H. pylori infection apparently suppresses their mRNA as well as receptor expression that is reversed by H. pylori eradication. This deficiency of the gastroprotective EGF system may contribute to the gastric pathogenicity of H. pylori infection.</description><subject>Adult</subject><subject>Amphiregulin</subject><subject>Bacterial diseases</subject><subject>Bacterial diseases of the digestive system and abdomen</subject><subject>Betacellulin</subject><subject>Biological and medical sciences</subject><subject>EGF Family of Proteins</subject><subject>Epidermal Growth Factor - biosynthesis</subject><subject>Epidermal Growth Factor Epidermal Growth Factor Receptor Ligands Helicobacter Pylori</subject><subject>ErbB Receptors - biosynthesis</subject><subject>Female</subject><subject>Gastric Mucosa - metabolism</subject><subject>Gastric Mucosa - microbiology</subject><subject>Gastritis - metabolism</subject><subject>Gastritis - microbiology</subject><subject>Glycoproteins - biosynthesis</subject><subject>GPI-Linked Proteins</subject><subject>Growth Substances - biosynthesis</subject><subject>Helicobacter Infections - metabolism</subject><subject>Helicobacter pylori</subject><subject>Heparin-binding EGF-like Growth Factor</subject><subject>Human bacterial diseases</subject><subject>Humans</subject><subject>Infectious diseases</subject><subject>Intercellular Signaling Peptides and Proteins</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Membrane Glycoproteins</subject><subject>Neoplasm Proteins - biosynthesis</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>RNA, Messenger - genetics</subject><subject>Transforming Growth Factor alpha - biosynthesis</subject><issn>0036-5521</issn><issn>1502-7708</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><recordid>eNp1kE1r3DAQhkVpaLZprz0WQaE3JyPZsq1jSDebwCaBkJ7NWB53FWzLlWzSnPrXK7Pblhxy0sc87_DyMPZJwKmAEs4A0lwpCUKCzuENWwkFMikKKN-y1TJM4lQcs_chPAKAKjL9jh0LIUUp03zFfn8j4wkDNXz9a_QUgnUDdy1fj7Yh32PHN949TTt-iWZynt-ToXG54NDw_v72fIGvp8C39kf8CtwO_Io6a1wdA-T5-Nw5bxM7tBTfDd9gmLw1_GY2LuAHdtRiF-jj4Txh3y_XDxdXyfZuc31xvk2MzFWemFbVWhuhiMBkujENpbWq87bGTEpdGJ1mRZphmSskmQOiBqGbFEjnaVSTnrCv-72jdz9nClPV22Co63AgN4eqAKWjHBHB0z1ovAvBU1uN3vbonysB1aK8eqk8Bj4fNs91T81__OA4Al8OAAaDXetxMDb848oyK-VSUO-pKMpF70_Od0014WLvbyR9tUL5Irsj7KadQU_Vo5v9EMW-1v4PEGSsVw</recordid><startdate>2001</startdate><enddate>2001</enddate><creator>SCHIEMANN, U</creator><creator>KONTUREK, J. 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W ; OSTERHOFF, M ; ASSERT, R ; REMBIASZ, K ; PFEIFFER, D ; SCHATZ, H ; DOMSCHKE, W ; PFEIFFER, A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2656-cf5b99c15ee0c49dcde3b5b6fba42297c934734a865ae260aa9019d30e9632093</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Adult</topic><topic>Amphiregulin</topic><topic>Bacterial diseases</topic><topic>Bacterial diseases of the digestive system and abdomen</topic><topic>Betacellulin</topic><topic>Biological and medical sciences</topic><topic>EGF Family of Proteins</topic><topic>Epidermal Growth Factor - biosynthesis</topic><topic>Epidermal Growth Factor Epidermal Growth Factor Receptor Ligands Helicobacter Pylori</topic><topic>ErbB Receptors - biosynthesis</topic><topic>Female</topic><topic>Gastric Mucosa - metabolism</topic><topic>Gastric Mucosa - microbiology</topic><topic>Gastritis - metabolism</topic><topic>Gastritis - microbiology</topic><topic>Glycoproteins - biosynthesis</topic><topic>GPI-Linked Proteins</topic><topic>Growth Substances - biosynthesis</topic><topic>Helicobacter Infections - metabolism</topic><topic>Helicobacter pylori</topic><topic>Heparin-binding EGF-like Growth Factor</topic><topic>Human bacterial diseases</topic><topic>Humans</topic><topic>Infectious diseases</topic><topic>Intercellular Signaling Peptides and Proteins</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Membrane Glycoproteins</topic><topic>Neoplasm Proteins - biosynthesis</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>RNA, Messenger - genetics</topic><topic>Transforming Growth Factor alpha - biosynthesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>SCHIEMANN, U</creatorcontrib><creatorcontrib>KONTUREK, J. 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W</au><au>OSTERHOFF, M</au><au>ASSERT, R</au><au>REMBIASZ, K</au><au>PFEIFFER, D</au><au>SCHATZ, H</au><au>DOMSCHKE, W</au><au>PFEIFFER, A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Decreased Expression of Epidermal Growth Factor Receptor and mRNA of Its Ligands in Helicobacter pylori-infected Gastric Mucosa</atitle><jtitle>Scandinavian journal of gastroenterology</jtitle><addtitle>Scand J Gastroenterol</addtitle><date>2001</date><risdate>2001</risdate><volume>36</volume><issue>1</issue><spage>23</spage><epage>31</epage><pages>23-31</pages><issn>0036-5521</issn><eissn>1502-7708</eissn><coden>SJGRA4</coden><abstract>Epidermal growth factor (EGF) and TGF-alpha play a central role in maintaining gastric mucosal integrity. Little is known about the regulative role of the four other widely expressed epidermal growth factor receptor ligands, heparin-binding EGF, amphiregulin, betacellulin and cripto in the gastric mucosa.
Nineteen patients with Helicobacter pylori-positive gastritis and 32 healthy controls were investigated. Mucosal mRNA expression of EGF receptor ligands was determined by quantitative PCR before and after H. pylori eradication. PCR products were analyzed by soft laser scanning densitometry. Moreover, the effect of chronic active gastritis on EGF receptor expression was assessed by [125I] EGF receptor autoradiography. Immunohistochemistry was performed for TGF-alpha to localize growth factor expression.
Antral and oxyntic biopsies showed strong mRNA expressions for TGF-alpha, amphiregulin and heparin binding EGF, but not for EGF, cripto and betacellulin. mRNA expression was significantly reduced down to 50% in H. pylori infection, significantly lower compared to normal gastric mucosa, and increased after eradication therapy. Moreover, chronic gastritis was associated with decreased antral EGF receptor binding compared to healthy controls, possibly reflecting reduced autoinduction. Immunohistochemical analyses localized TGF-alpha in the cytoplasma of gastric epithelial cells and revealed its increased expression after H. pylori eradication.
The data presented suggest that amphiregulin, heparin binding EGF and TGF-alpha are important EGF receptor ligands in the gastric mucosa. H. pylori infection apparently suppresses their mRNA as well as receptor expression that is reversed by H. pylori eradication. This deficiency of the gastroprotective EGF system may contribute to the gastric pathogenicity of H. pylori infection.</abstract><cop>Copenhagen</cop><cop>Oslo</cop><cop>Stockholm</cop><pub>Informa UK Ltd</pub><pmid>11218236</pmid><doi>10.1080/00365520120960</doi><tpages>9</tpages></addata></record> |
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subjects | Adult Amphiregulin Bacterial diseases Bacterial diseases of the digestive system and abdomen Betacellulin Biological and medical sciences EGF Family of Proteins Epidermal Growth Factor - biosynthesis Epidermal Growth Factor Epidermal Growth Factor Receptor Ligands Helicobacter Pylori ErbB Receptors - biosynthesis Female Gastric Mucosa - metabolism Gastric Mucosa - microbiology Gastritis - metabolism Gastritis - microbiology Glycoproteins - biosynthesis GPI-Linked Proteins Growth Substances - biosynthesis Helicobacter Infections - metabolism Helicobacter pylori Heparin-binding EGF-like Growth Factor Human bacterial diseases Humans Infectious diseases Intercellular Signaling Peptides and Proteins Male Medical sciences Membrane Glycoproteins Neoplasm Proteins - biosynthesis Reverse Transcriptase Polymerase Chain Reaction RNA, Messenger - genetics Transforming Growth Factor alpha - biosynthesis |
title | Decreased Expression of Epidermal Growth Factor Receptor and mRNA of Its Ligands in Helicobacter pylori-infected Gastric Mucosa |
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