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CDX-2 homeobox gene expression in human gastric carcinoma and precursor lesions
Background: Recent studies have demonstrated that CDX‐2 is expressed in the intestinal metaplasia of the stomach and intestinal‐type gastric cancer. To address the role of CDX‐2 in carcinogenesis of gastric carcinomas of intestinal type, the expression of CDX‐2 in gastric carcinoma and precursor le...
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Published in: | Journal of gastroenterology and hepatology 2006-02, Vol.21 (2), p.438-442 |
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creator | KIM, HYUNG-SEOK LEE, JI-SHIN FREUND, JEAN-NOEL MIN, KYUNG-WHAN LEE, JEONG-SOO KIM, WAN JUHNG, SANG-WOO PARK, CHANG-SOO |
description | Background: Recent studies have demonstrated that CDX‐2 is expressed in the intestinal metaplasia of the stomach and intestinal‐type gastric cancer. To address the role of CDX‐2 in carcinogenesis of gastric carcinomas of intestinal type, the expression of CDX‐2 in gastric carcinoma and precursor lesions were examined using immunohistochemistry.
Methods: A total of 160 specimens diagnosed as gastric carcinomas or non‐invasive neoplasia from 158 patients were analyzed for CDX‐2 expression by immunochemical methods. Patients were classified into histopathologic subgroups according to the Padova international classification: 60 cases of low‐grade non‐invasive neoplasia, 55 cases of high grade, and 45 cases of invasive intestinal‐type adenocarcinoma. The CDX‐2 expression in non‐neoplastic gastric mucosa including intestinal metaplasia was also evaluated in the areas included in the histologic sections.
Results: The CDX‐2 expression was localized in the epithelial cell nuclei in the area of intestinal metaplasia with or without dysplasia and carcinoma, consistent with its role as a transcriptional regulator. No CDX‐2 reactivity was noted in the normal mucosa in all cases. The CDX‐2 expression was detected in 73.3% of low‐grade cases, 85.5% of high‐grade cases and 91.1% of intestinal‐type adenocarcinoma cases. In the gastric mucosa with intestinal metaplasia, 89.7% of the samples were positive. The CDX‐2‐expressing cells in intestinal metaplasia were more prevalent than in dysplasia and carcinoma. Expression of CDX‐2 showed a statistically significant positive correlation with increasing grade of dysplasia and carcinoma.
Conclusions: These findings suggest that CDX‐2 expression in stomach cancer may be a marker of the progression of gastric carcinogenesis, and that its activation may represent an early event.
© 2005 Blackwell Publishing Asia Pty Ltd |
doi_str_mv | 10.1111/j.1440-1746.2005.03933.x |
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fullrecord | <record><control><sourceid>wiley_hal_p</sourceid><recordid>TN_cdi_hal_primary_oai_HAL_hal_03812876v1</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>JGH3933</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4693-857ff2d5b3f366ee0d15c83a88eca13360affcaec9b1f64b02d32bf7d078916e3</originalsourceid><addsrcrecordid>eNqNkE1P2zAYgC3EBB3wF5AvO3BIZueNP3LYgZXRbqpASKDtZjmOTd3lo7LpFv79kqUqV3yxZT_PK-tBCFOS0mF93qQ0z0lCRc7TjBCWEigA0v4IzQ4Px2hGJGVJAbQ4RR9j3BBCciLYCTqlnJFCCjpD9_ObX0mG111ju7Lr8bNtLbb9NtgYfddi3-L1rtEtftbxJXiDjQ7Gt12jsW4rPHBmF2IXcG1HPp6jD07X0V7s9zP0dPvtcb5MVveL7_PrVWJyXkAimXAuq1gJDji3llSUGQlaSms0BeBEO2e0NUVJHc9LklWQlU5URMiCcgtn6Gqau9a12gbf6PCqOu3V8nqlxjsCkmZS8D90YOXEmtDFGKw7CJSosafaqDGbGrOpsaf631P1g3o5qdtd2djqTdwHHIBPe0BHo2sXdGt8fOMEzzkIPnBfJu6vr-3ruz-gfiyW42nwk8n38cX2B1-H34oLEEz9vFsMpvzK4BbUA_wDsgqfHQ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>CDX-2 homeobox gene expression in human gastric carcinoma and precursor lesions</title><source>Wiley:Jisc Collections:Wiley Read and Publish Open Access 2024-2025 (reading list)</source><creator>KIM, HYUNG-SEOK ; LEE, JI-SHIN ; FREUND, JEAN-NOEL ; MIN, KYUNG-WHAN ; LEE, JEONG-SOO ; KIM, WAN ; JUHNG, SANG-WOO ; PARK, CHANG-SOO</creator><creatorcontrib>KIM, HYUNG-SEOK ; LEE, JI-SHIN ; FREUND, JEAN-NOEL ; MIN, KYUNG-WHAN ; LEE, JEONG-SOO ; KIM, WAN ; JUHNG, SANG-WOO ; PARK, CHANG-SOO</creatorcontrib><description>Background: Recent studies have demonstrated that CDX‐2 is expressed in the intestinal metaplasia of the stomach and intestinal‐type gastric cancer. To address the role of CDX‐2 in carcinogenesis of gastric carcinomas of intestinal type, the expression of CDX‐2 in gastric carcinoma and precursor lesions were examined using immunohistochemistry.
Methods: A total of 160 specimens diagnosed as gastric carcinomas or non‐invasive neoplasia from 158 patients were analyzed for CDX‐2 expression by immunochemical methods. Patients were classified into histopathologic subgroups according to the Padova international classification: 60 cases of low‐grade non‐invasive neoplasia, 55 cases of high grade, and 45 cases of invasive intestinal‐type adenocarcinoma. The CDX‐2 expression in non‐neoplastic gastric mucosa including intestinal metaplasia was also evaluated in the areas included in the histologic sections.
Results: The CDX‐2 expression was localized in the epithelial cell nuclei in the area of intestinal metaplasia with or without dysplasia and carcinoma, consistent with its role as a transcriptional regulator. No CDX‐2 reactivity was noted in the normal mucosa in all cases. The CDX‐2 expression was detected in 73.3% of low‐grade cases, 85.5% of high‐grade cases and 91.1% of intestinal‐type adenocarcinoma cases. In the gastric mucosa with intestinal metaplasia, 89.7% of the samples were positive. The CDX‐2‐expressing cells in intestinal metaplasia were more prevalent than in dysplasia and carcinoma. Expression of CDX‐2 showed a statistically significant positive correlation with increasing grade of dysplasia and carcinoma.
Conclusions: These findings suggest that CDX‐2 expression in stomach cancer may be a marker of the progression of gastric carcinogenesis, and that its activation may represent an early event.
© 2005 Blackwell Publishing Asia Pty Ltd</description><identifier>ISSN: 0815-9319</identifier><identifier>EISSN: 1440-1746</identifier><identifier>DOI: 10.1111/j.1440-1746.2005.03933.x</identifier><identifier>PMID: 16509871</identifier><language>eng</language><publisher>Melbourne, Australia: Blackwell Science Pty</publisher><subject>adenocarcinoma ; Adenocarcinoma - genetics ; Adenocarcinoma - metabolism ; Adenocarcinoma - pathology ; Aged ; Biological and medical sciences ; Biomarkers, Tumor ; Biopsy ; CDX-2 ; CDX2 Transcription Factor ; Cellular Biology ; DNA, Neoplasm - genetics ; Female ; Gastric Mucosa - metabolism ; Gastric Mucosa - pathology ; Gastroenterology. Liver. Pancreas. Abdomen ; Gene Expression Regulation, Neoplastic ; Homeodomain Proteins - biosynthesis ; Homeodomain Proteins - genetics ; Humans ; Immunohistochemistry ; Life Sciences ; Male ; Medical sciences ; Middle Aged ; non-invasive neoplasia ; Precancerous Conditions - genetics ; Precancerous Conditions - metabolism ; Precancerous Conditions - pathology ; Prognosis ; Retrospective Studies ; stomach ; Stomach Neoplasms - genetics ; Stomach Neoplasms - metabolism ; Stomach Neoplasms - pathology ; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus ; Tumors</subject><ispartof>Journal of gastroenterology and hepatology, 2006-02, Vol.21 (2), p.438-442</ispartof><rights>2006 INIST-CNRS</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4693-857ff2d5b3f366ee0d15c83a88eca13360affcaec9b1f64b02d32bf7d078916e3</citedby><cites>FETCH-LOGICAL-c4693-857ff2d5b3f366ee0d15c83a88eca13360affcaec9b1f64b02d32bf7d078916e3</cites><orcidid>0000-0002-0971-3774</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17646376$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16509871$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-03812876$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>KIM, HYUNG-SEOK</creatorcontrib><creatorcontrib>LEE, JI-SHIN</creatorcontrib><creatorcontrib>FREUND, JEAN-NOEL</creatorcontrib><creatorcontrib>MIN, KYUNG-WHAN</creatorcontrib><creatorcontrib>LEE, JEONG-SOO</creatorcontrib><creatorcontrib>KIM, WAN</creatorcontrib><creatorcontrib>JUHNG, SANG-WOO</creatorcontrib><creatorcontrib>PARK, CHANG-SOO</creatorcontrib><title>CDX-2 homeobox gene expression in human gastric carcinoma and precursor lesions</title><title>Journal of gastroenterology and hepatology</title><addtitle>J Gastroenterol Hepatol</addtitle><description>Background: Recent studies have demonstrated that CDX‐2 is expressed in the intestinal metaplasia of the stomach and intestinal‐type gastric cancer. To address the role of CDX‐2 in carcinogenesis of gastric carcinomas of intestinal type, the expression of CDX‐2 in gastric carcinoma and precursor lesions were examined using immunohistochemistry.
Methods: A total of 160 specimens diagnosed as gastric carcinomas or non‐invasive neoplasia from 158 patients were analyzed for CDX‐2 expression by immunochemical methods. Patients were classified into histopathologic subgroups according to the Padova international classification: 60 cases of low‐grade non‐invasive neoplasia, 55 cases of high grade, and 45 cases of invasive intestinal‐type adenocarcinoma. The CDX‐2 expression in non‐neoplastic gastric mucosa including intestinal metaplasia was also evaluated in the areas included in the histologic sections.
Results: The CDX‐2 expression was localized in the epithelial cell nuclei in the area of intestinal metaplasia with or without dysplasia and carcinoma, consistent with its role as a transcriptional regulator. No CDX‐2 reactivity was noted in the normal mucosa in all cases. The CDX‐2 expression was detected in 73.3% of low‐grade cases, 85.5% of high‐grade cases and 91.1% of intestinal‐type adenocarcinoma cases. In the gastric mucosa with intestinal metaplasia, 89.7% of the samples were positive. The CDX‐2‐expressing cells in intestinal metaplasia were more prevalent than in dysplasia and carcinoma. Expression of CDX‐2 showed a statistically significant positive correlation with increasing grade of dysplasia and carcinoma.
Conclusions: These findings suggest that CDX‐2 expression in stomach cancer may be a marker of the progression of gastric carcinogenesis, and that its activation may represent an early event.
© 2005 Blackwell Publishing Asia Pty Ltd</description><subject>adenocarcinoma</subject><subject>Adenocarcinoma - genetics</subject><subject>Adenocarcinoma - metabolism</subject><subject>Adenocarcinoma - pathology</subject><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Biomarkers, Tumor</subject><subject>Biopsy</subject><subject>CDX-2</subject><subject>CDX2 Transcription Factor</subject><subject>Cellular Biology</subject><subject>DNA, Neoplasm - genetics</subject><subject>Female</subject><subject>Gastric Mucosa - metabolism</subject><subject>Gastric Mucosa - pathology</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Homeodomain Proteins - biosynthesis</subject><subject>Homeodomain Proteins - genetics</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Life Sciences</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>non-invasive neoplasia</subject><subject>Precancerous Conditions - genetics</subject><subject>Precancerous Conditions - metabolism</subject><subject>Precancerous Conditions - pathology</subject><subject>Prognosis</subject><subject>Retrospective Studies</subject><subject>stomach</subject><subject>Stomach Neoplasms - genetics</subject><subject>Stomach Neoplasms - metabolism</subject><subject>Stomach Neoplasms - pathology</subject><subject>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</subject><subject>Tumors</subject><issn>0815-9319</issn><issn>1440-1746</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNqNkE1P2zAYgC3EBB3wF5AvO3BIZueNP3LYgZXRbqpASKDtZjmOTd3lo7LpFv79kqUqV3yxZT_PK-tBCFOS0mF93qQ0z0lCRc7TjBCWEigA0v4IzQ4Px2hGJGVJAbQ4RR9j3BBCciLYCTqlnJFCCjpD9_ObX0mG111ju7Lr8bNtLbb9NtgYfddi3-L1rtEtftbxJXiDjQ7Gt12jsW4rPHBmF2IXcG1HPp6jD07X0V7s9zP0dPvtcb5MVveL7_PrVWJyXkAimXAuq1gJDji3llSUGQlaSms0BeBEO2e0NUVJHc9LklWQlU5URMiCcgtn6Gqau9a12gbf6PCqOu3V8nqlxjsCkmZS8D90YOXEmtDFGKw7CJSosafaqDGbGrOpsaf631P1g3o5qdtd2djqTdwHHIBPe0BHo2sXdGt8fOMEzzkIPnBfJu6vr-3ruz-gfiyW42nwk8n38cX2B1-H34oLEEz9vFsMpvzK4BbUA_wDsgqfHQ</recordid><startdate>200602</startdate><enddate>200602</enddate><creator>KIM, HYUNG-SEOK</creator><creator>LEE, JI-SHIN</creator><creator>FREUND, JEAN-NOEL</creator><creator>MIN, KYUNG-WHAN</creator><creator>LEE, JEONG-SOO</creator><creator>KIM, WAN</creator><creator>JUHNG, SANG-WOO</creator><creator>PARK, CHANG-SOO</creator><general>Blackwell Science Pty</general><general>Blackwell Science</general><general>Wiley</general><scope>BSCLL</scope><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>1XC</scope><orcidid>https://orcid.org/0000-0002-0971-3774</orcidid></search><sort><creationdate>200602</creationdate><title>CDX-2 homeobox gene expression in human gastric carcinoma and precursor lesions</title><author>KIM, HYUNG-SEOK ; LEE, JI-SHIN ; FREUND, JEAN-NOEL ; MIN, KYUNG-WHAN ; LEE, JEONG-SOO ; KIM, WAN ; JUHNG, SANG-WOO ; PARK, CHANG-SOO</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4693-857ff2d5b3f366ee0d15c83a88eca13360affcaec9b1f64b02d32bf7d078916e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>adenocarcinoma</topic><topic>Adenocarcinoma - genetics</topic><topic>Adenocarcinoma - metabolism</topic><topic>Adenocarcinoma - pathology</topic><topic>Aged</topic><topic>Biological and medical sciences</topic><topic>Biomarkers, Tumor</topic><topic>Biopsy</topic><topic>CDX-2</topic><topic>CDX2 Transcription Factor</topic><topic>Cellular Biology</topic><topic>DNA, Neoplasm - genetics</topic><topic>Female</topic><topic>Gastric Mucosa - metabolism</topic><topic>Gastric Mucosa - pathology</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Homeodomain Proteins - biosynthesis</topic><topic>Homeodomain Proteins - genetics</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Life Sciences</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>non-invasive neoplasia</topic><topic>Precancerous Conditions - genetics</topic><topic>Precancerous Conditions - metabolism</topic><topic>Precancerous Conditions - pathology</topic><topic>Prognosis</topic><topic>Retrospective Studies</topic><topic>stomach</topic><topic>Stomach Neoplasms - genetics</topic><topic>Stomach Neoplasms - metabolism</topic><topic>Stomach Neoplasms - pathology</topic><topic>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>KIM, HYUNG-SEOK</creatorcontrib><creatorcontrib>LEE, JI-SHIN</creatorcontrib><creatorcontrib>FREUND, JEAN-NOEL</creatorcontrib><creatorcontrib>MIN, KYUNG-WHAN</creatorcontrib><creatorcontrib>LEE, JEONG-SOO</creatorcontrib><creatorcontrib>KIM, WAN</creatorcontrib><creatorcontrib>JUHNG, SANG-WOO</creatorcontrib><creatorcontrib>PARK, CHANG-SOO</creatorcontrib><collection>Istex</collection><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>Hyper Article en Ligne (HAL)</collection><jtitle>Journal of gastroenterology and hepatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>KIM, HYUNG-SEOK</au><au>LEE, JI-SHIN</au><au>FREUND, JEAN-NOEL</au><au>MIN, KYUNG-WHAN</au><au>LEE, JEONG-SOO</au><au>KIM, WAN</au><au>JUHNG, SANG-WOO</au><au>PARK, CHANG-SOO</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>CDX-2 homeobox gene expression in human gastric carcinoma and precursor lesions</atitle><jtitle>Journal of gastroenterology and hepatology</jtitle><addtitle>J Gastroenterol Hepatol</addtitle><date>2006-02</date><risdate>2006</risdate><volume>21</volume><issue>2</issue><spage>438</spage><epage>442</epage><pages>438-442</pages><issn>0815-9319</issn><eissn>1440-1746</eissn><abstract>Background: Recent studies have demonstrated that CDX‐2 is expressed in the intestinal metaplasia of the stomach and intestinal‐type gastric cancer. To address the role of CDX‐2 in carcinogenesis of gastric carcinomas of intestinal type, the expression of CDX‐2 in gastric carcinoma and precursor lesions were examined using immunohistochemistry.
Methods: A total of 160 specimens diagnosed as gastric carcinomas or non‐invasive neoplasia from 158 patients were analyzed for CDX‐2 expression by immunochemical methods. Patients were classified into histopathologic subgroups according to the Padova international classification: 60 cases of low‐grade non‐invasive neoplasia, 55 cases of high grade, and 45 cases of invasive intestinal‐type adenocarcinoma. The CDX‐2 expression in non‐neoplastic gastric mucosa including intestinal metaplasia was also evaluated in the areas included in the histologic sections.
Results: The CDX‐2 expression was localized in the epithelial cell nuclei in the area of intestinal metaplasia with or without dysplasia and carcinoma, consistent with its role as a transcriptional regulator. No CDX‐2 reactivity was noted in the normal mucosa in all cases. The CDX‐2 expression was detected in 73.3% of low‐grade cases, 85.5% of high‐grade cases and 91.1% of intestinal‐type adenocarcinoma cases. In the gastric mucosa with intestinal metaplasia, 89.7% of the samples were positive. The CDX‐2‐expressing cells in intestinal metaplasia were more prevalent than in dysplasia and carcinoma. Expression of CDX‐2 showed a statistically significant positive correlation with increasing grade of dysplasia and carcinoma.
Conclusions: These findings suggest that CDX‐2 expression in stomach cancer may be a marker of the progression of gastric carcinogenesis, and that its activation may represent an early event.
© 2005 Blackwell Publishing Asia Pty Ltd</abstract><cop>Melbourne, Australia</cop><pub>Blackwell Science Pty</pub><pmid>16509871</pmid><doi>10.1111/j.1440-1746.2005.03933.x</doi><tpages>5</tpages><orcidid>https://orcid.org/0000-0002-0971-3774</orcidid></addata></record> |
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subjects | adenocarcinoma Adenocarcinoma - genetics Adenocarcinoma - metabolism Adenocarcinoma - pathology Aged Biological and medical sciences Biomarkers, Tumor Biopsy CDX-2 CDX2 Transcription Factor Cellular Biology DNA, Neoplasm - genetics Female Gastric Mucosa - metabolism Gastric Mucosa - pathology Gastroenterology. Liver. Pancreas. Abdomen Gene Expression Regulation, Neoplastic Homeodomain Proteins - biosynthesis Homeodomain Proteins - genetics Humans Immunohistochemistry Life Sciences Male Medical sciences Middle Aged non-invasive neoplasia Precancerous Conditions - genetics Precancerous Conditions - metabolism Precancerous Conditions - pathology Prognosis Retrospective Studies stomach Stomach Neoplasms - genetics Stomach Neoplasms - metabolism Stomach Neoplasms - pathology Stomach. Duodenum. Small intestine. Colon. Rectum. Anus Tumors |
title | CDX-2 homeobox gene expression in human gastric carcinoma and precursor lesions |
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