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Methylation of the oestrogen receptor gene in non-neoplastic epithelium as a marker of colorectal neoplasia risk in longstanding and extensive ulcerative colitis
Background: Surveillance colonoscopy is widely recommended in patients with longstanding and extensive ulcerative colitis (UC) in order to detect colorectal neoplasia at an early stage. However, it still remains questionable whether surveillance colonoscopy effectively enables early detection of UC...
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Published in: | Gut 2005-09, Vol.54 (9), p.1287-1292 |
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creator | Fujii, S Tominaga, K Kitajima, K Takeda, J Kusaka, T Fujita, M Ichikawa, K Tomita, S Ohkura, Y Ono, Y Imura, J Chiba, T Fujimori, T |
description | Background: Surveillance colonoscopy is widely recommended in patients with longstanding and extensive ulcerative colitis (UC) in order to detect colorectal neoplasia at an early stage. However, it still remains questionable whether surveillance colonoscopy effectively enables early detection of UC associated neoplasia. There is a great need for sensitive markers to identify individuals at increased risk of neoplasia. The oestrogen receptor (OR) gene shows age related methylation in the colorectal epithelium and is methylated frequently in sporadic colorectal neoplasia, suggesting that OR methylation may predispose to colorectal neoplasia. Aim: To clarify whether analysis of methylation of the OR gene in non-neoplastic epithelium can contribute to prediction of increased neoplasia risk in UC patients. Materials and methods: A total of 165 non-neoplastic colorectal epithelia from 30 patients with longstanding and extensive UC, including 13 UC patients with neoplasia and 17 patients without, were evaluated. Methylation specific polymerase chain reaction was performed to determine the methylation status of the OR gene. Results: Methylation of the OR gene was detected in 54 of 70 (77.1%) non-neoplastic colorectal epithelia in UC with neoplasia but in only 23 of 95 (24.2%) without neoplasia. Methylation of the OR gene was significantly more frequent in non-neoplastic epithelium from UC with neoplasia than in chronic colitic epithelium from UC without neoplasia. Furthermore, in UC with neoplasia, the OR gene was extensively methylated in non-neoplastic epithelia throughout the colorectum compared with those in UC without neoplasia. Conclusion: These results suggest that analysis of OR gene methylation may have potential as a useful marker for identifying individuals at increased risk of neoplasia among those with longstanding and extensive UC. |
doi_str_mv | 10.1136/gut.2004.062059 |
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However, it still remains questionable whether surveillance colonoscopy effectively enables early detection of UC associated neoplasia. There is a great need for sensitive markers to identify individuals at increased risk of neoplasia. The oestrogen receptor (OR) gene shows age related methylation in the colorectal epithelium and is methylated frequently in sporadic colorectal neoplasia, suggesting that OR methylation may predispose to colorectal neoplasia. Aim: To clarify whether analysis of methylation of the OR gene in non-neoplastic epithelium can contribute to prediction of increased neoplasia risk in UC patients. Materials and methods: A total of 165 non-neoplastic colorectal epithelia from 30 patients with longstanding and extensive UC, including 13 UC patients with neoplasia and 17 patients without, were evaluated. Methylation specific polymerase chain reaction was performed to determine the methylation status of the OR gene. Results: Methylation of the OR gene was detected in 54 of 70 (77.1%) non-neoplastic colorectal epithelia in UC with neoplasia but in only 23 of 95 (24.2%) without neoplasia. Methylation of the OR gene was significantly more frequent in non-neoplastic epithelium from UC with neoplasia than in chronic colitic epithelium from UC without neoplasia. Furthermore, in UC with neoplasia, the OR gene was extensively methylated in non-neoplastic epithelia throughout the colorectum compared with those in UC without neoplasia. Conclusion: These results suggest that analysis of OR gene methylation may have potential as a useful marker for identifying individuals at increased risk of neoplasia among those with longstanding and extensive UC.</description><identifier>ISSN: 0017-5749</identifier><identifier>EISSN: 1468-3288</identifier><identifier>EISSN: 1458-3288</identifier><identifier>DOI: 10.1136/gut.2004.062059</identifier><identifier>PMID: 15870230</identifier><identifier>CODEN: GUTTAK</identifier><language>eng</language><publisher>London: BMJ Publishing Group Ltd and British Society of Gastroenterology</publisher><subject>Age ; Aged ; Biological and medical sciences ; Biopsy ; Cancer ; Carcinogens ; Case-Control Studies ; Chi-Square Distribution ; Classification ; Colitis, Ulcerative - complications ; Colitis, Ulcerative - immunology ; Colitis, Ulcerative - metabolism ; Colon ; Colonic Neoplasms - complications ; Colonic Neoplasms - immunology ; Colonic Neoplasms - metabolism ; Colorectal Cancer ; Deoxyribonucleic acid ; Digestive system. Abdomen ; Disease Progression ; DNA ; DNA Methylation ; Endoscopy ; Female ; Gastroenterology ; Gastroenterology. Liver. Pancreas. Abdomen ; Genes ; Genetic Markers ; Hospitals ; Humans ; Inflammation ; Inflammatory bowel disease ; Intestinal Mucosa - metabolism ; Investigative techniques, diagnostic techniques (general aspects) ; Male ; Medical sciences ; Medicine ; methylation ; methylation specific polymerase chain reaction ; Middle Aged ; Mortality ; MSP ; neoplasia ; oestrogen receptor ; Other diseases. Semiology ; PCR ; Polymerase chain reaction ; Prognosis ; Receptors, Estrogen - genetics ; Receptors, Estrogen - metabolism ; Risk ; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus ; Surveillance ; Time Factors ; ulcerative colitis</subject><ispartof>Gut, 2005-09, Vol.54 (9), p.1287-1292</ispartof><rights>Copyright 2005 by Gut</rights><rights>2005 INIST-CNRS</rights><rights>Copyright: 2005 Copyright 2005 by Gut</rights><rights>Copyright © Copyright 2005 by Gut 2005</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b553t-5e281373f03e3a4c8a1ff22910a621efc4324380134f3413fe2b28c7434f7c0c3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1774644/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1774644/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17031045$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15870230$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fujii, S</creatorcontrib><creatorcontrib>Tominaga, K</creatorcontrib><creatorcontrib>Kitajima, K</creatorcontrib><creatorcontrib>Takeda, J</creatorcontrib><creatorcontrib>Kusaka, T</creatorcontrib><creatorcontrib>Fujita, M</creatorcontrib><creatorcontrib>Ichikawa, K</creatorcontrib><creatorcontrib>Tomita, S</creatorcontrib><creatorcontrib>Ohkura, Y</creatorcontrib><creatorcontrib>Ono, Y</creatorcontrib><creatorcontrib>Imura, J</creatorcontrib><creatorcontrib>Chiba, T</creatorcontrib><creatorcontrib>Fujimori, T</creatorcontrib><title>Methylation of the oestrogen receptor gene in non-neoplastic epithelium as a marker of colorectal neoplasia risk in longstanding and extensive ulcerative colitis</title><title>Gut</title><addtitle>Gut</addtitle><description>Background: Surveillance colonoscopy is widely recommended in patients with longstanding and extensive ulcerative colitis (UC) in order to detect colorectal neoplasia at an early stage. However, it still remains questionable whether surveillance colonoscopy effectively enables early detection of UC associated neoplasia. There is a great need for sensitive markers to identify individuals at increased risk of neoplasia. The oestrogen receptor (OR) gene shows age related methylation in the colorectal epithelium and is methylated frequently in sporadic colorectal neoplasia, suggesting that OR methylation may predispose to colorectal neoplasia. Aim: To clarify whether analysis of methylation of the OR gene in non-neoplastic epithelium can contribute to prediction of increased neoplasia risk in UC patients. Materials and methods: A total of 165 non-neoplastic colorectal epithelia from 30 patients with longstanding and extensive UC, including 13 UC patients with neoplasia and 17 patients without, were evaluated. Methylation specific polymerase chain reaction was performed to determine the methylation status of the OR gene. Results: Methylation of the OR gene was detected in 54 of 70 (77.1%) non-neoplastic colorectal epithelia in UC with neoplasia but in only 23 of 95 (24.2%) without neoplasia. Methylation of the OR gene was significantly more frequent in non-neoplastic epithelium from UC with neoplasia than in chronic colitic epithelium from UC without neoplasia. Furthermore, in UC with neoplasia, the OR gene was extensively methylated in non-neoplastic epithelia throughout the colorectum compared with those in UC without neoplasia. Conclusion: These results suggest that analysis of OR gene methylation may have potential as a useful marker for identifying individuals at increased risk of neoplasia among those with longstanding and extensive UC.</description><subject>Age</subject><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Biopsy</subject><subject>Cancer</subject><subject>Carcinogens</subject><subject>Case-Control Studies</subject><subject>Chi-Square Distribution</subject><subject>Classification</subject><subject>Colitis, Ulcerative - complications</subject><subject>Colitis, Ulcerative - immunology</subject><subject>Colitis, Ulcerative - metabolism</subject><subject>Colon</subject><subject>Colonic Neoplasms - complications</subject><subject>Colonic Neoplasms - immunology</subject><subject>Colonic Neoplasms - metabolism</subject><subject>Colorectal Cancer</subject><subject>Deoxyribonucleic acid</subject><subject>Digestive system. Abdomen</subject><subject>Disease Progression</subject><subject>DNA</subject><subject>DNA Methylation</subject><subject>Endoscopy</subject><subject>Female</subject><subject>Gastroenterology</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Genes</subject><subject>Genetic Markers</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Inflammation</subject><subject>Inflammatory bowel disease</subject><subject>Intestinal Mucosa - metabolism</subject><subject>Investigative techniques, diagnostic techniques (general aspects)</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Medicine</subject><subject>methylation</subject><subject>methylation specific polymerase chain reaction</subject><subject>Middle Aged</subject><subject>Mortality</subject><subject>MSP</subject><subject>neoplasia</subject><subject>oestrogen receptor</subject><subject>Other diseases. Semiology</subject><subject>PCR</subject><subject>Polymerase chain reaction</subject><subject>Prognosis</subject><subject>Receptors, Estrogen - genetics</subject><subject>Receptors, Estrogen - metabolism</subject><subject>Risk</subject><subject>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</subject><subject>Surveillance</subject><subject>Time Factors</subject><subject>ulcerative colitis</subject><issn>0017-5749</issn><issn>1468-3288</issn><issn>1458-3288</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNqFkktvEzEQx1cIREPhzA1ZQnBA2tTPtfdSCYW3ykM8euBiOe5s4tSxg-2t2o_DN8VRoha49DQezW_-nhn9m-YxwVNCWHe0GMuUYsynuKNY9HeaCeGdahlV6m4zwZjIVkjeHzQPcl5hjJXqyf3mgAglMWV40vz-CGV55U1xMaA4oLIEFCGXFBcQUAILmxITqgkgF1CIoQ0QN97k4iyCjasN3o1rZDIyaG3SOaStjo0-1u5iPNrzzqDk8vlWxcewyMWEMxcWqAYElwVCdheARm8h1Wnqs0q44vLD5t5gfIZH-3jY_Hjz-vvsXXvy-e372cuTdi4EK60AqgiTbMAMmOFWGTIMlPYEm44SGCxnlDOFCeMD44QNQOdUWclrLi227LA53uluxvkaziyEkozXm-TqVlc6Gqf_rQS31It4oYmUvOO8CjzfC6T4a6w31GuXLXhv6gXGrDvFFWaS3ApSQpQQQlbw6X_gKo4p1CtsP-0ZI1x1lTraUTbFnBMM1zMTrLcu0dUleusSvXNJ7Xjy96o3_N4WFXi2B0y2xg_JBOvyDScxI5iLyrU7zuUCl9f16gLdSSaF_nQ60z8_fH01-9J_06eVf7Hj5-vVrVP-AVoA5ZA</recordid><startdate>20050901</startdate><enddate>20050901</enddate><creator>Fujii, S</creator><creator>Tominaga, K</creator><creator>Kitajima, K</creator><creator>Takeda, J</creator><creator>Kusaka, T</creator><creator>Fujita, M</creator><creator>Ichikawa, K</creator><creator>Tomita, S</creator><creator>Ohkura, Y</creator><creator>Ono, Y</creator><creator>Imura, J</creator><creator>Chiba, T</creator><creator>Fujimori, T</creator><general>BMJ Publishing Group Ltd and British Society of Gastroenterology</general><general>BMJ</general><general>BMJ Publishing Group LTD</general><general>Copyright 2005 by Gut</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20050901</creationdate><title>Methylation of the oestrogen receptor gene in non-neoplastic epithelium as a marker of colorectal neoplasia risk in longstanding and extensive ulcerative colitis</title><author>Fujii, S ; Tominaga, K ; Kitajima, K ; Takeda, J ; Kusaka, T ; Fujita, M ; Ichikawa, K ; Tomita, S ; Ohkura, Y ; Ono, Y ; Imura, J ; Chiba, T ; Fujimori, T</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b553t-5e281373f03e3a4c8a1ff22910a621efc4324380134f3413fe2b28c7434f7c0c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Age</topic><topic>Aged</topic><topic>Biological and medical sciences</topic><topic>Biopsy</topic><topic>Cancer</topic><topic>Carcinogens</topic><topic>Case-Control Studies</topic><topic>Chi-Square Distribution</topic><topic>Classification</topic><topic>Colitis, Ulcerative - complications</topic><topic>Colitis, Ulcerative - immunology</topic><topic>Colitis, Ulcerative - metabolism</topic><topic>Colon</topic><topic>Colonic Neoplasms - complications</topic><topic>Colonic Neoplasms - immunology</topic><topic>Colonic Neoplasms - metabolism</topic><topic>Colorectal Cancer</topic><topic>Deoxyribonucleic acid</topic><topic>Digestive system. Abdomen</topic><topic>Disease Progression</topic><topic>DNA</topic><topic>DNA Methylation</topic><topic>Endoscopy</topic><topic>Female</topic><topic>Gastroenterology</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Genes</topic><topic>Genetic Markers</topic><topic>Hospitals</topic><topic>Humans</topic><topic>Inflammation</topic><topic>Inflammatory bowel disease</topic><topic>Intestinal Mucosa - metabolism</topic><topic>Investigative techniques, diagnostic techniques (general aspects)</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Medicine</topic><topic>methylation</topic><topic>methylation specific polymerase chain reaction</topic><topic>Middle Aged</topic><topic>Mortality</topic><topic>MSP</topic><topic>neoplasia</topic><topic>oestrogen receptor</topic><topic>Other diseases. Semiology</topic><topic>PCR</topic><topic>Polymerase chain reaction</topic><topic>Prognosis</topic><topic>Receptors, Estrogen - genetics</topic><topic>Receptors, Estrogen - metabolism</topic><topic>Risk</topic><topic>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</topic><topic>Surveillance</topic><topic>Time Factors</topic><topic>ulcerative colitis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fujii, S</creatorcontrib><creatorcontrib>Tominaga, K</creatorcontrib><creatorcontrib>Kitajima, K</creatorcontrib><creatorcontrib>Takeda, J</creatorcontrib><creatorcontrib>Kusaka, T</creatorcontrib><creatorcontrib>Fujita, M</creatorcontrib><creatorcontrib>Ichikawa, K</creatorcontrib><creatorcontrib>Tomita, S</creatorcontrib><creatorcontrib>Ohkura, Y</creatorcontrib><creatorcontrib>Ono, Y</creatorcontrib><creatorcontrib>Imura, J</creatorcontrib><creatorcontrib>Chiba, T</creatorcontrib><creatorcontrib>Fujimori, T</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>ProQuest Central (Corporate)</collection><collection>ProQuest_Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</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)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest Science Journals</collection><collection>Biological Science Database</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>ProQuest Central Basic</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Gut</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fujii, S</au><au>Tominaga, K</au><au>Kitajima, K</au><au>Takeda, J</au><au>Kusaka, T</au><au>Fujita, M</au><au>Ichikawa, K</au><au>Tomita, S</au><au>Ohkura, Y</au><au>Ono, Y</au><au>Imura, J</au><au>Chiba, T</au><au>Fujimori, T</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Methylation of the oestrogen receptor gene in non-neoplastic epithelium as a marker of colorectal neoplasia risk in longstanding and extensive ulcerative colitis</atitle><jtitle>Gut</jtitle><addtitle>Gut</addtitle><date>2005-09-01</date><risdate>2005</risdate><volume>54</volume><issue>9</issue><spage>1287</spage><epage>1292</epage><pages>1287-1292</pages><issn>0017-5749</issn><eissn>1468-3288</eissn><eissn>1458-3288</eissn><coden>GUTTAK</coden><abstract>Background: Surveillance colonoscopy is widely recommended in patients with longstanding and extensive ulcerative colitis (UC) in order to detect colorectal neoplasia at an early stage. However, it still remains questionable whether surveillance colonoscopy effectively enables early detection of UC associated neoplasia. There is a great need for sensitive markers to identify individuals at increased risk of neoplasia. The oestrogen receptor (OR) gene shows age related methylation in the colorectal epithelium and is methylated frequently in sporadic colorectal neoplasia, suggesting that OR methylation may predispose to colorectal neoplasia. Aim: To clarify whether analysis of methylation of the OR gene in non-neoplastic epithelium can contribute to prediction of increased neoplasia risk in UC patients. Materials and methods: A total of 165 non-neoplastic colorectal epithelia from 30 patients with longstanding and extensive UC, including 13 UC patients with neoplasia and 17 patients without, were evaluated. Methylation specific polymerase chain reaction was performed to determine the methylation status of the OR gene. Results: Methylation of the OR gene was detected in 54 of 70 (77.1%) non-neoplastic colorectal epithelia in UC with neoplasia but in only 23 of 95 (24.2%) without neoplasia. Methylation of the OR gene was significantly more frequent in non-neoplastic epithelium from UC with neoplasia than in chronic colitic epithelium from UC without neoplasia. Furthermore, in UC with neoplasia, the OR gene was extensively methylated in non-neoplastic epithelia throughout the colorectum compared with those in UC without neoplasia. Conclusion: These results suggest that analysis of OR gene methylation may have potential as a useful marker for identifying individuals at increased risk of neoplasia among those with longstanding and extensive UC.</abstract><cop>London</cop><pub>BMJ Publishing Group Ltd and British Society of Gastroenterology</pub><pmid>15870230</pmid><doi>10.1136/gut.2004.062059</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Age Aged Biological and medical sciences Biopsy Cancer Carcinogens Case-Control Studies Chi-Square Distribution Classification Colitis, Ulcerative - complications Colitis, Ulcerative - immunology Colitis, Ulcerative - metabolism Colon Colonic Neoplasms - complications Colonic Neoplasms - immunology Colonic Neoplasms - metabolism Colorectal Cancer Deoxyribonucleic acid Digestive system. Abdomen Disease Progression DNA DNA Methylation Endoscopy Female Gastroenterology Gastroenterology. Liver. Pancreas. Abdomen Genes Genetic Markers Hospitals Humans Inflammation Inflammatory bowel disease Intestinal Mucosa - metabolism Investigative techniques, diagnostic techniques (general aspects) Male Medical sciences Medicine methylation methylation specific polymerase chain reaction Middle Aged Mortality MSP neoplasia oestrogen receptor Other diseases. Semiology PCR Polymerase chain reaction Prognosis Receptors, Estrogen - genetics Receptors, Estrogen - metabolism Risk Stomach. Duodenum. Small intestine. Colon. Rectum. Anus Surveillance Time Factors ulcerative colitis |
title | Methylation of the oestrogen receptor gene in non-neoplastic epithelium as a marker of colorectal neoplasia risk in longstanding and extensive ulcerative colitis |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-05T06%3A58%3A46IST&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=Methylation%20of%20the%20oestrogen%20receptor%20gene%20in%20non-neoplastic%20epithelium%20as%20a%20marker%20of%20colorectal%20neoplasia%20risk%20in%20longstanding%20and%20extensive%20ulcerative%20colitis&rft.jtitle=Gut&rft.au=Fujii,%20S&rft.date=2005-09-01&rft.volume=54&rft.issue=9&rft.spage=1287&rft.epage=1292&rft.pages=1287-1292&rft.issn=0017-5749&rft.eissn=1468-3288&rft.coden=GUTTAK&rft_id=info:doi/10.1136/gut.2004.062059&rft_dat=%3Cproquest_pubme%3E68480371%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-b553t-5e281373f03e3a4c8a1ff22910a621efc4324380134f3413fe2b28c7434f7c0c3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1779331486&rft_id=info:pmid/15870230&rfr_iscdi=true |