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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
Main Authors: 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
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container_issue 9
container_start_page 1287
container_title Gut
container_volume 54
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&amp;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. 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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.</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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1458-3288
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source Open Access: PubMed Central
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