Loading…
CpG island methylator phenotype and Helicobacterpylori infection associated with gastric cancer
AIM: To investigate the association between the CpG island methylator phenotype (CIMP) and serum Helico- bacter pylori (H. pylori) levels for clinical prediction of gastric cancer (GC) progression. METHODS: We analyzed the serum ClMP status of 75 patients with GC using a methylation marker panel and...
Saved in:
Published in: | 世界胃肠病学杂志:英文版 2012, Vol.18 (36), p.5129-5134 |
---|---|
Main Author: | |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | |
container_end_page | 5134 |
container_issue | 36 |
container_start_page | 5129 |
container_title | 世界胃肠病学杂志:英文版 |
container_volume | 18 |
creator | Ji-Bin Liu Xu-Ming Wu Jin Cai Jin-Ye Zhang Jin-Lin Zhang Shu-Hui Zhou Min-Xin Shi Fu-Lin Qiang |
description | AIM: To investigate the association between the CpG island methylator phenotype (CIMP) and serum Helico- bacter pylori (H. pylori) levels for clinical prediction of gastric cancer (GC) progression. METHODS: We analyzed the serum ClMP status of 75 patients with GC using a methylation marker panel and a methylation-specific polymerase chain reaction. Serum samples from 40 healthy persons were examined at the same time. The genes examined were APC, WIF-1, RUNX-3, DLC-1, SFRP-1, DKK and E-cad. H. pylori infec- tion in serum was assayed with an anti-H, pylori immu- noglobulin G antibody test and a rapid urease test. RESULTS: The frequencies of high-level methylation in GC tissues for the seven genes were: 48% for APC, 57.33% for WIF-1, 56% for RUNX-3, 50.67% for DLC-1, 52% for SFRP-1, 54.67% for DKK, and 48% for E-cad.The frequencies in GC serum were 30.67% for APC, 34.67% for WIF-1, 37.33% for RUNX-3, 29.33% for DLC-1, 33.33% for SFRP-1, 32% for DKK, and 26.67% for E-cad. CIMP+ (defined as ≥ 3 methylated genes) was associated with 47 (62.67%) GC tissue samples and 44 (58.67%) GC serum samples. CIMP+ was not associated with non-neoplastic mucosal tissues or the serum of healthy persons. Of the 75 GC cases, 51 (68%) were H. pylori+, and 24 (32%) were H. pylori-. Of the 51 H. pylori+ cases, 36 were CIMP+ and 15 were CIMP-. In contrast, for the 24 H. pylori- cases, 11 were CIMP+, and 13 were CIMP-. The difference was signifi- cant between the H. pylori+ and H. pylori- groups χ2 = 4.27, P 〈 0.05). Of the 51 H. pylori+ GC patients, 34 were CIMP+ and 17 were CIMP-, while among the 24 H. pylori- GC cases, 10 were CIMP+ and 14 were CIMP-. The difference was significant between the H. pylori+ and H. pylori- groups (χ2 = 4.21, P 〈 0.05). A 2-year follow-up showed significant difference in the rates of metastasis and recurrence between H. pylori+/CIMP+ cases and the H. pylori+/CIMP- cases or CIMP- cases associated with H. pylori assayed in serum (P 〈 0.05). However, there were no significant differences in sur- vival rates between the two groups. CONCLUSION: H. pylori+/CIMP+ cases are associ- ated with higher rates of metastasis and recurrence thanH, pylori+/CIMP- cases. Serum may be useful for examining CIMP status. |
format | article |
fullrecord | <record><control><sourceid>chongqing</sourceid><recordid>TN_cdi_chongqing_primary_43530943</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><cqvip_id>43530943</cqvip_id><sourcerecordid>43530943</sourcerecordid><originalsourceid>FETCH-chongqing_primary_435309433</originalsourceid><addsrcrecordid>eNqNyksKwjAQgOEgCtbHHcYDFGJSqV0XHwdwX8Y4tiMxiUlAensRPICrf_H9E1EotW1Kta_kVBRbKeuy0aqei0VKDymV1jtViK4NJ-Bk0d3gSXkYLWYfIQzkfB4DwRfOZNn4K5pMMYzWRwZ2dzKZvQNMyRvGTDd4cx6gx5QjGzDoDMWVmN3RJlr_uhSb4-HSnkszeNe_2PVdiPzEOHaV3mnZVFr_83wAHiNFnQ</addsrcrecordid><sourcetype>Publisher</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>CpG island methylator phenotype and Helicobacterpylori infection associated with gastric cancer</title><source>PubMed Central Free</source><creator>Ji-Bin Liu Xu-Ming Wu Jin Cai Jin-Ye Zhang Jin-Lin Zhang Shu-Hui Zhou Min-Xin Shi Fu-Lin Qiang</creator><creatorcontrib>Ji-Bin Liu Xu-Ming Wu Jin Cai Jin-Ye Zhang Jin-Lin Zhang Shu-Hui Zhou Min-Xin Shi Fu-Lin Qiang</creatorcontrib><description>AIM: To investigate the association between the CpG island methylator phenotype (CIMP) and serum Helico- bacter pylori (H. pylori) levels for clinical prediction of gastric cancer (GC) progression. METHODS: We analyzed the serum ClMP status of 75 patients with GC using a methylation marker panel and a methylation-specific polymerase chain reaction. Serum samples from 40 healthy persons were examined at the same time. The genes examined were APC, WIF-1, RUNX-3, DLC-1, SFRP-1, DKK and E-cad. H. pylori infec- tion in serum was assayed with an anti-H, pylori immu- noglobulin G antibody test and a rapid urease test. RESULTS: The frequencies of high-level methylation in GC tissues for the seven genes were: 48% for APC, 57.33% for WIF-1, 56% for RUNX-3, 50.67% for DLC-1, 52% for SFRP-1, 54.67% for DKK, and 48% for E-cad.The frequencies in GC serum were 30.67% for APC, 34.67% for WIF-1, 37.33% for RUNX-3, 29.33% for DLC-1, 33.33% for SFRP-1, 32% for DKK, and 26.67% for E-cad. CIMP+ (defined as ≥ 3 methylated genes) was associated with 47 (62.67%) GC tissue samples and 44 (58.67%) GC serum samples. CIMP+ was not associated with non-neoplastic mucosal tissues or the serum of healthy persons. Of the 75 GC cases, 51 (68%) were H. pylori+, and 24 (32%) were H. pylori-. Of the 51 H. pylori+ cases, 36 were CIMP+ and 15 were CIMP-. In contrast, for the 24 H. pylori- cases, 11 were CIMP+, and 13 were CIMP-. The difference was signifi- cant between the H. pylori+ and H. pylori- groups χ2 = 4.27, P 〈 0.05). Of the 51 H. pylori+ GC patients, 34 were CIMP+ and 17 were CIMP-, while among the 24 H. pylori- GC cases, 10 were CIMP+ and 14 were CIMP-. The difference was significant between the H. pylori+ and H. pylori- groups (χ2 = 4.21, P 〈 0.05). A 2-year follow-up showed significant difference in the rates of metastasis and recurrence between H. pylori+/CIMP+ cases and the H. pylori+/CIMP- cases or CIMP- cases associated with H. pylori assayed in serum (P 〈 0.05). However, there were no significant differences in sur- vival rates between the two groups. CONCLUSION: H. pylori+/CIMP+ cases are associ- ated with higher rates of metastasis and recurrence thanH, pylori+/CIMP- cases. Serum may be useful for examining CIMP status.</description><identifier>ISSN: 1007-9327</identifier><identifier>EISSN: 2219-2840</identifier><language>eng</language><subject>CpG岛 ; 基因甲基化 ; 幽门螺旋杆菌 ; 幽门螺杆菌 ; 感染 ; 胃癌 ; 血清样品 ; 表型</subject><ispartof>世界胃肠病学杂志:英文版, 2012, Vol.18 (36), p.5129-5134</ispartof><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/84123X/84123X.jpg</thumbnail><link.rule.ids>314,780,784,4024</link.rule.ids></links><search><creatorcontrib>Ji-Bin Liu Xu-Ming Wu Jin Cai Jin-Ye Zhang Jin-Lin Zhang Shu-Hui Zhou Min-Xin Shi Fu-Lin Qiang</creatorcontrib><title>CpG island methylator phenotype and Helicobacterpylori infection associated with gastric cancer</title><title>世界胃肠病学杂志:英文版</title><addtitle>World Journal of Gastroenterology</addtitle><description>AIM: To investigate the association between the CpG island methylator phenotype (CIMP) and serum Helico- bacter pylori (H. pylori) levels for clinical prediction of gastric cancer (GC) progression. METHODS: We analyzed the serum ClMP status of 75 patients with GC using a methylation marker panel and a methylation-specific polymerase chain reaction. Serum samples from 40 healthy persons were examined at the same time. The genes examined were APC, WIF-1, RUNX-3, DLC-1, SFRP-1, DKK and E-cad. H. pylori infec- tion in serum was assayed with an anti-H, pylori immu- noglobulin G antibody test and a rapid urease test. RESULTS: The frequencies of high-level methylation in GC tissues for the seven genes were: 48% for APC, 57.33% for WIF-1, 56% for RUNX-3, 50.67% for DLC-1, 52% for SFRP-1, 54.67% for DKK, and 48% for E-cad.The frequencies in GC serum were 30.67% for APC, 34.67% for WIF-1, 37.33% for RUNX-3, 29.33% for DLC-1, 33.33% for SFRP-1, 32% for DKK, and 26.67% for E-cad. CIMP+ (defined as ≥ 3 methylated genes) was associated with 47 (62.67%) GC tissue samples and 44 (58.67%) GC serum samples. CIMP+ was not associated with non-neoplastic mucosal tissues or the serum of healthy persons. Of the 75 GC cases, 51 (68%) were H. pylori+, and 24 (32%) were H. pylori-. Of the 51 H. pylori+ cases, 36 were CIMP+ and 15 were CIMP-. In contrast, for the 24 H. pylori- cases, 11 were CIMP+, and 13 were CIMP-. The difference was signifi- cant between the H. pylori+ and H. pylori- groups χ2 = 4.27, P 〈 0.05). Of the 51 H. pylori+ GC patients, 34 were CIMP+ and 17 were CIMP-, while among the 24 H. pylori- GC cases, 10 were CIMP+ and 14 were CIMP-. The difference was significant between the H. pylori+ and H. pylori- groups (χ2 = 4.21, P 〈 0.05). A 2-year follow-up showed significant difference in the rates of metastasis and recurrence between H. pylori+/CIMP+ cases and the H. pylori+/CIMP- cases or CIMP- cases associated with H. pylori assayed in serum (P 〈 0.05). However, there were no significant differences in sur- vival rates between the two groups. CONCLUSION: H. pylori+/CIMP+ cases are associ- ated with higher rates of metastasis and recurrence thanH, pylori+/CIMP- cases. Serum may be useful for examining CIMP status.</description><subject>CpG岛</subject><subject>基因甲基化</subject><subject>幽门螺旋杆菌</subject><subject>幽门螺杆菌</subject><subject>感染</subject><subject>胃癌</subject><subject>血清样品</subject><subject>表型</subject><issn>1007-9327</issn><issn>2219-2840</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNqNyksKwjAQgOEgCtbHHcYDFGJSqV0XHwdwX8Y4tiMxiUlAensRPICrf_H9E1EotW1Kta_kVBRbKeuy0aqei0VKDymV1jtViK4NJ-Bk0d3gSXkYLWYfIQzkfB4DwRfOZNn4K5pMMYzWRwZ2dzKZvQNMyRvGTDd4cx6gx5QjGzDoDMWVmN3RJlr_uhSb4-HSnkszeNe_2PVdiPzEOHaV3mnZVFr_83wAHiNFnQ</recordid><startdate>2012</startdate><enddate>2012</enddate><creator>Ji-Bin Liu Xu-Ming Wu Jin Cai Jin-Ye Zhang Jin-Lin Zhang Shu-Hui Zhou Min-Xin Shi Fu-Lin Qiang</creator><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>W91</scope><scope>~WA</scope></search><sort><creationdate>2012</creationdate><title>CpG island methylator phenotype and Helicobacterpylori infection associated with gastric cancer</title><author>Ji-Bin Liu Xu-Ming Wu Jin Cai Jin-Ye Zhang Jin-Lin Zhang Shu-Hui Zhou Min-Xin Shi Fu-Lin Qiang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-chongqing_primary_435309433</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>CpG岛</topic><topic>基因甲基化</topic><topic>幽门螺旋杆菌</topic><topic>幽门螺杆菌</topic><topic>感染</topic><topic>胃癌</topic><topic>血清样品</topic><topic>表型</topic><toplevel>online_resources</toplevel><creatorcontrib>Ji-Bin Liu Xu-Ming Wu Jin Cai Jin-Ye Zhang Jin-Lin Zhang Shu-Hui Zhou Min-Xin Shi Fu-Lin Qiang</creatorcontrib><collection>维普_期刊</collection><collection>中文科技期刊数据库-CALIS站点</collection><collection>维普中文期刊数据库</collection><collection>中文科技期刊数据库-医药卫生</collection><collection>中文科技期刊数据库- 镜像站点</collection><jtitle>世界胃肠病学杂志:英文版</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ji-Bin Liu Xu-Ming Wu Jin Cai Jin-Ye Zhang Jin-Lin Zhang Shu-Hui Zhou Min-Xin Shi Fu-Lin Qiang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>CpG island methylator phenotype and Helicobacterpylori infection associated with gastric cancer</atitle><jtitle>世界胃肠病学杂志:英文版</jtitle><addtitle>World Journal of Gastroenterology</addtitle><date>2012</date><risdate>2012</risdate><volume>18</volume><issue>36</issue><spage>5129</spage><epage>5134</epage><pages>5129-5134</pages><issn>1007-9327</issn><eissn>2219-2840</eissn><abstract>AIM: To investigate the association between the CpG island methylator phenotype (CIMP) and serum Helico- bacter pylori (H. pylori) levels for clinical prediction of gastric cancer (GC) progression. METHODS: We analyzed the serum ClMP status of 75 patients with GC using a methylation marker panel and a methylation-specific polymerase chain reaction. Serum samples from 40 healthy persons were examined at the same time. The genes examined were APC, WIF-1, RUNX-3, DLC-1, SFRP-1, DKK and E-cad. H. pylori infec- tion in serum was assayed with an anti-H, pylori immu- noglobulin G antibody test and a rapid urease test. RESULTS: The frequencies of high-level methylation in GC tissues for the seven genes were: 48% for APC, 57.33% for WIF-1, 56% for RUNX-3, 50.67% for DLC-1, 52% for SFRP-1, 54.67% for DKK, and 48% for E-cad.The frequencies in GC serum were 30.67% for APC, 34.67% for WIF-1, 37.33% for RUNX-3, 29.33% for DLC-1, 33.33% for SFRP-1, 32% for DKK, and 26.67% for E-cad. CIMP+ (defined as ≥ 3 methylated genes) was associated with 47 (62.67%) GC tissue samples and 44 (58.67%) GC serum samples. CIMP+ was not associated with non-neoplastic mucosal tissues or the serum of healthy persons. Of the 75 GC cases, 51 (68%) were H. pylori+, and 24 (32%) were H. pylori-. Of the 51 H. pylori+ cases, 36 were CIMP+ and 15 were CIMP-. In contrast, for the 24 H. pylori- cases, 11 were CIMP+, and 13 were CIMP-. The difference was signifi- cant between the H. pylori+ and H. pylori- groups χ2 = 4.27, P 〈 0.05). Of the 51 H. pylori+ GC patients, 34 were CIMP+ and 17 were CIMP-, while among the 24 H. pylori- GC cases, 10 were CIMP+ and 14 were CIMP-. The difference was significant between the H. pylori+ and H. pylori- groups (χ2 = 4.21, P 〈 0.05). A 2-year follow-up showed significant difference in the rates of metastasis and recurrence between H. pylori+/CIMP+ cases and the H. pylori+/CIMP- cases or CIMP- cases associated with H. pylori assayed in serum (P 〈 0.05). However, there were no significant differences in sur- vival rates between the two groups. CONCLUSION: H. pylori+/CIMP+ cases are associ- ated with higher rates of metastasis and recurrence thanH, pylori+/CIMP- cases. Serum may be useful for examining CIMP status.</abstract></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1007-9327 |
ispartof | 世界胃肠病学杂志:英文版, 2012, Vol.18 (36), p.5129-5134 |
issn | 1007-9327 2219-2840 |
language | eng |
recordid | cdi_chongqing_primary_43530943 |
source | PubMed Central Free |
subjects | CpG岛 基因甲基化 幽门螺旋杆菌 幽门螺杆菌 感染 胃癌 血清样品 表型 |
title | CpG island methylator phenotype and Helicobacterpylori infection associated with gastric cancer |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-30T13%3A35%3A58IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-chongqing&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=CpG%20island%20methylator%20phenotype%20and%20Helicobacterpylori%20infection%20associated%20with%20gastric%20cancer&rft.jtitle=%E4%B8%96%E7%95%8C%E8%83%83%E8%82%A0%E7%97%85%E5%AD%A6%E6%9D%82%E5%BF%97%EF%BC%9A%E8%8B%B1%E6%96%87%E7%89%88&rft.au=Ji-Bin%20Liu%20Xu-Ming%20Wu%20Jin%20Cai%20Jin-Ye%20Zhang%20Jin-Lin%20Zhang%20Shu-Hui%20Zhou%20Min-Xin%20Shi%20Fu-Lin%20Qiang&rft.date=2012&rft.volume=18&rft.issue=36&rft.spage=5129&rft.epage=5134&rft.pages=5129-5134&rft.issn=1007-9327&rft.eissn=2219-2840&rft_id=info:doi/&rft_dat=%3Cchongqing%3E43530943%3C/chongqing%3E%3Cgrp_id%3Ecdi_FETCH-chongqing_primary_435309433%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rft_cqvip_id=43530943&rfr_iscdi=true |