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- Publisher Website: 10.1002/path.1741
- Scopus: eid_2-s2.0-17144418415
- PMID: 15732140
- WOS: WOS:000228197200010
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Article: CDX2 co-localizes with liver-intestine cadherin in intestinal metaplasia and adenocarcinoma of the stomach
Title | CDX2 co-localizes with liver-intestine cadherin in intestinal metaplasia and adenocarcinoma of the stomach |
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Authors | |
Keywords | CDX2 Gastric adenocarcinoma Immunohistochemistry Intestinal metaplasia LI-cadherin RT-PCR |
Issue Date | 2005 |
Publisher | John Wiley & Sons. The Journal's web site is located at http://www3.interscience.wiley.com/cgi-bin/jhome/1130 |
Citation | Journal of Pathology, 2005, v. 205 n. 5, p. 615-622 How to Cite? |
Abstract | CDX2 and liver-intestine (LI)-cadherin are intestine-specific markers and both are physiologically expressed in the small intestine and colon. Recent studies have demonstrated that CDX2 regulates LI-cadherin gene (CDH17) expression in colorectal cancer. The present study investigated the relationship of CDX2 and LI-cadherin expression in gastric cancer. One hundred and nine pairs of tumour and non-cancerous gastric mucosa were collected from gastrectomy specimens. Protein expression levels of CDX2 and LI-cadherin were determined by immunohistochemical staining. Semi-quantitative RT-PCR showed that the mRNAs of both CDX2 and CDH17 were highly expressed in tumour compared with non-cancerous mucosa. Overexpression of CDX2 was significantly associated with CDH17 in gastric adenocarcinoma. Furthermore, the expression of CDX2 and LI-cadherin proteins was strongly coupled in intestinal metaplasia. In conclusion, overexpression of CDH-17 is significantly associated with CDX2. Copyright © 2005 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd. |
Persistent Identifier | http://hdl.handle.net/10722/148402 |
ISSN | 2023 Impact Factor: 5.6 2023 SCImago Journal Rankings: 2.426 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
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dc.contributor.author | Ko, S | en_HK |
dc.contributor.author | Chu, KM | en_HK |
dc.contributor.author | Luk, JMC | en_HK |
dc.contributor.author | Wong, BWY | en_HK |
dc.contributor.author | Yuen, ST | en_HK |
dc.contributor.author | Leung, SY | en_HK |
dc.contributor.author | Wong, J | en_HK |
dc.date.accessioned | 2012-05-29T06:12:45Z | - |
dc.date.available | 2012-05-29T06:12:45Z | - |
dc.date.issued | 2005 | en_HK |
dc.identifier.citation | Journal of Pathology, 2005, v. 205 n. 5, p. 615-622 | en_HK |
dc.identifier.issn | 0022-3417 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/148402 | - |
dc.description.abstract | CDX2 and liver-intestine (LI)-cadherin are intestine-specific markers and both are physiologically expressed in the small intestine and colon. Recent studies have demonstrated that CDX2 regulates LI-cadherin gene (CDH17) expression in colorectal cancer. The present study investigated the relationship of CDX2 and LI-cadherin expression in gastric cancer. One hundred and nine pairs of tumour and non-cancerous gastric mucosa were collected from gastrectomy specimens. Protein expression levels of CDX2 and LI-cadherin were determined by immunohistochemical staining. Semi-quantitative RT-PCR showed that the mRNAs of both CDX2 and CDH17 were highly expressed in tumour compared with non-cancerous mucosa. Overexpression of CDX2 was significantly associated with CDH17 in gastric adenocarcinoma. Furthermore, the expression of CDX2 and LI-cadherin proteins was strongly coupled in intestinal metaplasia. In conclusion, overexpression of CDH-17 is significantly associated with CDX2. Copyright © 2005 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd. | en_HK |
dc.language | eng | en_US |
dc.publisher | John Wiley & Sons. The Journal's web site is located at http://www3.interscience.wiley.com/cgi-bin/jhome/1130 | en_HK |
dc.relation.ispartof | Journal of Pathology | en_HK |
dc.rights | Journal of Pathology. Copyright © John Wiley & Sons Ltd. | - |
dc.subject | CDX2 | en_HK |
dc.subject | Gastric adenocarcinoma | en_HK |
dc.subject | Immunohistochemistry | en_HK |
dc.subject | Intestinal metaplasia | en_HK |
dc.subject | LI-cadherin | en_HK |
dc.subject | RT-PCR | en_HK |
dc.subject.mesh | Adenocarcinoma - Metabolism - Pathology | en_US |
dc.subject.mesh | Adult | en_US |
dc.subject.mesh | Aged | en_US |
dc.subject.mesh | Aged, 80 And Over | en_US |
dc.subject.mesh | Cadherins - Genetics - Metabolism | en_US |
dc.subject.mesh | Disease Progression | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Homeodomain Proteins - Genetics - Metabolism | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Immunoenzyme Techniques | en_US |
dc.subject.mesh | Lymphatic Metastasis | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Metaplasia - Metabolism | en_US |
dc.subject.mesh | Middle Aged | en_US |
dc.subject.mesh | Neoplasm Proteins - Genetics - Metabolism | en_US |
dc.subject.mesh | Neoplasm Staging | en_US |
dc.subject.mesh | Precancerous Conditions - Metabolism | en_US |
dc.subject.mesh | Rna, Messenger - Genetics | en_US |
dc.subject.mesh | Reverse Transcriptase Polymerase Chain Reaction - Methods | en_US |
dc.subject.mesh | Stomach - Pathology | en_US |
dc.subject.mesh | Stomach Neoplasms - Metabolism - Pathology | en_US |
dc.subject.mesh | Tumor Markers, Biological - Genetics - Metabolism | en_US |
dc.subject.mesh | Up-Regulation | en_US |
dc.title | CDX2 co-localizes with liver-intestine cadherin in intestinal metaplasia and adenocarcinoma of the stomach | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Chu, KM: chukm@hkucc.hku.hk | en_HK |
dc.identifier.email | Luk, JMC: jmluk@hkucc.hku.hk | en_HK |
dc.identifier.email | Yuen, ST: styuen@hkucc.hku.hk | en_HK |
dc.identifier.email | Leung, SY: suetyi@hku.hk | en_HK |
dc.identifier.email | Wong, J: jwong@hkucc.hku.hk | - |
dc.identifier.authority | Chu, KM=rp00435 | en_HK |
dc.identifier.authority | Luk, JMC=rp00349 | en_HK |
dc.identifier.authority | Leung, SY=rp00359 | en_HK |
dc.identifier.authority | Wong, J=rp00322 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1002/path.1741 | en_HK |
dc.identifier.pmid | 15732140 | - |
dc.identifier.scopus | eid_2-s2.0-17144418415 | en_HK |
dc.identifier.hkuros | 97604 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-17144418415&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 205 | en_HK |
dc.identifier.issue | 5 | en_HK |
dc.identifier.spage | 615 | en_HK |
dc.identifier.epage | 622 | en_HK |
dc.identifier.isi | WOS:000228197200010 | - |
dc.publisher.place | United Kingdom | en_HK |
dc.identifier.scopusauthorid | Ko, S=7403326231 | en_HK |
dc.identifier.scopusauthorid | Chu, KM=7402453538 | en_HK |
dc.identifier.scopusauthorid | Luk, JMC=7006777791 | en_HK |
dc.identifier.scopusauthorid | Wong, BWY=8602085500 | en_HK |
dc.identifier.scopusauthorid | Yuen, ST=7103160927 | en_HK |
dc.identifier.scopusauthorid | Leung, SY=7202044886 | en_HK |
dc.identifier.scopusauthorid | Wong, J=8049324500 | en_HK |
dc.identifier.citeulike | 139054 | - |
dc.customcontrol.immutable | sml 130621 | - |
dc.identifier.issnl | 0022-3417 | - |