Loading…
Current evidence on the relationship between four polymorphisms in the matrix metalloproteinases (MMP) gene and breast cancer risk: a meta-analysis
The matrix metalloproteinases (MMP) can degrade various components of the extracellular matrix and its functional genetic polymorphisms may be associated with breast cancer risk. However, this relationship remains controversial. A meta-analysis was conducted in order to investigate the potential ass...
Saved in:
Published in: | Breast cancer research and treatment 2011-06, Vol.127 (3), p.813-818 |
---|---|
Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c498t-9d1f27f2716145af8d37cdac1f58059557040f21b0f0cbfe7896c5dd6d6863113 |
---|---|
cites | cdi_FETCH-LOGICAL-c498t-9d1f27f2716145af8d37cdac1f58059557040f21b0f0cbfe7896c5dd6d6863113 |
container_end_page | 818 |
container_issue | 3 |
container_start_page | 813 |
container_title | Breast cancer research and treatment |
container_volume | 127 |
creator | Zhou, Ping Du, Liang-Feng Lv, Guo-Qiang Yu, Xian-Ming Gu, Yuan-Long Li, Jian-Ping Zhang, Chun |
description | The matrix metalloproteinases (MMP) can degrade various components of the extracellular matrix and its functional genetic polymorphisms may be associated with breast cancer risk. However, this relationship remains controversial. A meta-analysis was conducted in order to investigate the potential association between four polymorphisms in the MMP gene and breast cancer risk. A database search yielded a total of 9 studies involving 2,597 cases and 2,618 controls. Four polymorphisms were included in the meta-analysis: MMP-1 −1607 2G/1G (rs1799750), MMP-2 −1306 C/T (rs243865), MMP-3 −1171 6A/5A (rs3025058) and MMP-9 −1562 C/T (rs3918242). Crude odds ratios (OR) with 95% confidence intervals (CI) were used to assess the strength of association. When all the studies were pooled into the meta-analysis, we found that breast cancer cases had a significantly higher frequency of CC genotype (OR = 1.27, 95% CI = 1.10, 1.47;
P
= 0.001) and lower frequency of CT genotype (OR = 0.78, 95% CI = 0.67, 0.91;
P
= 0.001) of MMP-2. No significant difference was found in any genotype of MMP-1, MMP-3 or MMP-9. In conclusion, this meta-analysis suggested that MMP-2 −1306 C/T polymorphism may contribute to breast cancer susceptibility. More studies were needed especially in Asians in the future. |
doi_str_mv | 10.1007/s10549-010-1294-0 |
format | article |
fullrecord | <record><control><sourceid>gale_proqu</sourceid><recordid>TN_cdi_proquest_miscellaneous_868030764</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A356142747</galeid><sourcerecordid>A356142747</sourcerecordid><originalsourceid>FETCH-LOGICAL-c498t-9d1f27f2716145af8d37cdac1f58059557040f21b0f0cbfe7896c5dd6d6863113</originalsourceid><addsrcrecordid>eNp1kstu1DAUhiMEokPhAdggC8RtkXKcmxN21Yib1AoWsI48zvGMi2MPPg4wz8EL42kGShHIlizb33_uWXafwwkHEC-IQ111OXDIedFVOdzIFrwWZS4KLm5mC-CNyJsWmqPsDtEFAHQCutvZUcF5w8umW2Q_llMI6CLDr2ZAp5B5x-IGWUAro_GONmbLVhi_ITqm_RTY1tvd6MN2Y2gkZmZ8lDGY72zEKK312-AjGicJiT07P__wnK3RIZNuYKuAkiJTMvkKLBj6_JLJS10unbQ7MnQ3u6WlJbx3OI-zT69ffVy-zc_ev3m3PD3LVdW1Me8GrguRdsqlqqVuh1KoQSqu6xbqrq4FVKALvgINaqVRtF2j6mFohqZtSs7L4-zpbDeF-2VCiv1oSKG10qGfqG9T6UoQTZXIh3-RF6kSKdwEiZaXRdXuzT2aobW02BunfQxS7U32p2WdYixEJRJ18g8qrQFHo7xDbdL7NcGTPwQblDZuyNvpsjnXQT6DKniigLrfBjPKsOs59Pt56ed56WF_T_PSQ9I8OCQ2rUYcfit-DUgCHh8ASUpaHVLfDF1xVVHWCUxcMXOUvtwaw1WF_u_9J9Nj1p4</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>878132481</pqid></control><display><type>article</type><title>Current evidence on the relationship between four polymorphisms in the matrix metalloproteinases (MMP) gene and breast cancer risk: a meta-analysis</title><source>Springer Nature</source><creator>Zhou, Ping ; Du, Liang-Feng ; Lv, Guo-Qiang ; Yu, Xian-Ming ; Gu, Yuan-Long ; Li, Jian-Ping ; Zhang, Chun</creator><creatorcontrib>Zhou, Ping ; Du, Liang-Feng ; Lv, Guo-Qiang ; Yu, Xian-Ming ; Gu, Yuan-Long ; Li, Jian-Ping ; Zhang, Chun</creatorcontrib><description>The matrix metalloproteinases (MMP) can degrade various components of the extracellular matrix and its functional genetic polymorphisms may be associated with breast cancer risk. However, this relationship remains controversial. A meta-analysis was conducted in order to investigate the potential association between four polymorphisms in the MMP gene and breast cancer risk. A database search yielded a total of 9 studies involving 2,597 cases and 2,618 controls. Four polymorphisms were included in the meta-analysis: MMP-1 −1607 2G/1G (rs1799750), MMP-2 −1306 C/T (rs243865), MMP-3 −1171 6A/5A (rs3025058) and MMP-9 −1562 C/T (rs3918242). Crude odds ratios (OR) with 95% confidence intervals (CI) were used to assess the strength of association. When all the studies were pooled into the meta-analysis, we found that breast cancer cases had a significantly higher frequency of CC genotype (OR = 1.27, 95% CI = 1.10, 1.47;
P
= 0.001) and lower frequency of CT genotype (OR = 0.78, 95% CI = 0.67, 0.91;
P
= 0.001) of MMP-2. No significant difference was found in any genotype of MMP-1, MMP-3 or MMP-9. In conclusion, this meta-analysis suggested that MMP-2 −1306 C/T polymorphism may contribute to breast cancer susceptibility. More studies were needed especially in Asians in the future.</description><identifier>ISSN: 0167-6806</identifier><identifier>EISSN: 1573-7217</identifier><identifier>DOI: 10.1007/s10549-010-1294-0</identifier><identifier>PMID: 21161369</identifier><identifier>CODEN: BCTRD6</identifier><language>eng</language><publisher>Boston: Springer US</publisher><subject>Biological and medical sciences ; Breast cancer ; Breast Neoplasms - genetics ; Cancer ; Cancer research ; Epidemiology ; Female ; Genes ; Genetic aspects ; Genetic Association Studies ; Genetic Predisposition to Disease ; Genotype ; Gynecology. Andrology. Obstetrics ; Health aspects ; Humans ; Mammary gland diseases ; Matrix Metalloproteinases - genetics ; Medical sciences ; Medicine ; Medicine & Public Health ; Meta-analysis ; Odds Ratio ; Oncology ; Polymorphism ; Polymorphism, Single Nucleotide ; Promoter Regions, Genetic ; Risk ; Risk factors ; Tumors</subject><ispartof>Breast cancer research and treatment, 2011-06, Vol.127 (3), p.813-818</ispartof><rights>Springer Science+Business Media, LLC. 2010</rights><rights>2015 INIST-CNRS</rights><rights>COPYRIGHT 2011 Springer</rights><rights>Springer Science+Business Media, LLC. 2011</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c498t-9d1f27f2716145af8d37cdac1f58059557040f21b0f0cbfe7896c5dd6d6863113</citedby><cites>FETCH-LOGICAL-c498t-9d1f27f2716145af8d37cdac1f58059557040f21b0f0cbfe7896c5dd6d6863113</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24235136$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21161369$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhou, Ping</creatorcontrib><creatorcontrib>Du, Liang-Feng</creatorcontrib><creatorcontrib>Lv, Guo-Qiang</creatorcontrib><creatorcontrib>Yu, Xian-Ming</creatorcontrib><creatorcontrib>Gu, Yuan-Long</creatorcontrib><creatorcontrib>Li, Jian-Ping</creatorcontrib><creatorcontrib>Zhang, Chun</creatorcontrib><title>Current evidence on the relationship between four polymorphisms in the matrix metalloproteinases (MMP) gene and breast cancer risk: a meta-analysis</title><title>Breast cancer research and treatment</title><addtitle>Breast Cancer Res Treat</addtitle><addtitle>Breast Cancer Res Treat</addtitle><description>The matrix metalloproteinases (MMP) can degrade various components of the extracellular matrix and its functional genetic polymorphisms may be associated with breast cancer risk. However, this relationship remains controversial. A meta-analysis was conducted in order to investigate the potential association between four polymorphisms in the MMP gene and breast cancer risk. A database search yielded a total of 9 studies involving 2,597 cases and 2,618 controls. Four polymorphisms were included in the meta-analysis: MMP-1 −1607 2G/1G (rs1799750), MMP-2 −1306 C/T (rs243865), MMP-3 −1171 6A/5A (rs3025058) and MMP-9 −1562 C/T (rs3918242). Crude odds ratios (OR) with 95% confidence intervals (CI) were used to assess the strength of association. When all the studies were pooled into the meta-analysis, we found that breast cancer cases had a significantly higher frequency of CC genotype (OR = 1.27, 95% CI = 1.10, 1.47;
P
= 0.001) and lower frequency of CT genotype (OR = 0.78, 95% CI = 0.67, 0.91;
P
= 0.001) of MMP-2. No significant difference was found in any genotype of MMP-1, MMP-3 or MMP-9. In conclusion, this meta-analysis suggested that MMP-2 −1306 C/T polymorphism may contribute to breast cancer susceptibility. More studies were needed especially in Asians in the future.</description><subject>Biological and medical sciences</subject><subject>Breast cancer</subject><subject>Breast Neoplasms - genetics</subject><subject>Cancer</subject><subject>Cancer research</subject><subject>Epidemiology</subject><subject>Female</subject><subject>Genes</subject><subject>Genetic aspects</subject><subject>Genetic Association Studies</subject><subject>Genetic Predisposition to Disease</subject><subject>Genotype</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Health aspects</subject><subject>Humans</subject><subject>Mammary gland diseases</subject><subject>Matrix Metalloproteinases - genetics</subject><subject>Medical sciences</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Meta-analysis</subject><subject>Odds Ratio</subject><subject>Oncology</subject><subject>Polymorphism</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Promoter Regions, Genetic</subject><subject>Risk</subject><subject>Risk factors</subject><subject>Tumors</subject><issn>0167-6806</issn><issn>1573-7217</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNp1kstu1DAUhiMEokPhAdggC8RtkXKcmxN21Yib1AoWsI48zvGMi2MPPg4wz8EL42kGShHIlizb33_uWXafwwkHEC-IQ111OXDIedFVOdzIFrwWZS4KLm5mC-CNyJsWmqPsDtEFAHQCutvZUcF5w8umW2Q_llMI6CLDr2ZAp5B5x-IGWUAro_GONmbLVhi_ITqm_RTY1tvd6MN2Y2gkZmZ8lDGY72zEKK312-AjGicJiT07P__wnK3RIZNuYKuAkiJTMvkKLBj6_JLJS10unbQ7MnQ3u6WlJbx3OI-zT69ffVy-zc_ev3m3PD3LVdW1Me8GrguRdsqlqqVuh1KoQSqu6xbqrq4FVKALvgINaqVRtF2j6mFohqZtSs7L4-zpbDeF-2VCiv1oSKG10qGfqG9T6UoQTZXIh3-RF6kSKdwEiZaXRdXuzT2aobW02BunfQxS7U32p2WdYixEJRJ18g8qrQFHo7xDbdL7NcGTPwQblDZuyNvpsjnXQT6DKniigLrfBjPKsOs59Pt56ed56WF_T_PSQ9I8OCQ2rUYcfit-DUgCHh8ASUpaHVLfDF1xVVHWCUxcMXOUvtwaw1WF_u_9J9Nj1p4</recordid><startdate>20110601</startdate><enddate>20110601</enddate><creator>Zhou, Ping</creator><creator>Du, Liang-Feng</creator><creator>Lv, Guo-Qiang</creator><creator>Yu, Xian-Ming</creator><creator>Gu, Yuan-Long</creator><creator>Li, Jian-Ping</creator><creator>Zhang, Chun</creator><general>Springer US</general><general>Springer</general><general>Springer Nature B.V</general><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>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>K9-</scope><scope>K9.</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20110601</creationdate><title>Current evidence on the relationship between four polymorphisms in the matrix metalloproteinases (MMP) gene and breast cancer risk: a meta-analysis</title><author>Zhou, Ping ; Du, Liang-Feng ; Lv, Guo-Qiang ; Yu, Xian-Ming ; Gu, Yuan-Long ; Li, Jian-Ping ; Zhang, Chun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c498t-9d1f27f2716145af8d37cdac1f58059557040f21b0f0cbfe7896c5dd6d6863113</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Biological and medical sciences</topic><topic>Breast cancer</topic><topic>Breast Neoplasms - genetics</topic><topic>Cancer</topic><topic>Cancer research</topic><topic>Epidemiology</topic><topic>Female</topic><topic>Genes</topic><topic>Genetic aspects</topic><topic>Genetic Association Studies</topic><topic>Genetic Predisposition to Disease</topic><topic>Genotype</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Health aspects</topic><topic>Humans</topic><topic>Mammary gland diseases</topic><topic>Matrix Metalloproteinases - genetics</topic><topic>Medical sciences</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Meta-analysis</topic><topic>Odds Ratio</topic><topic>Oncology</topic><topic>Polymorphism</topic><topic>Polymorphism, Single Nucleotide</topic><topic>Promoter Regions, Genetic</topic><topic>Risk</topic><topic>Risk factors</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhou, Ping</creatorcontrib><creatorcontrib>Du, Liang-Feng</creatorcontrib><creatorcontrib>Lv, Guo-Qiang</creatorcontrib><creatorcontrib>Yu, Xian-Ming</creatorcontrib><creatorcontrib>Gu, Yuan-Long</creatorcontrib><creatorcontrib>Li, Jian-Ping</creatorcontrib><creatorcontrib>Zhang, Chun</creatorcontrib><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>Oncogenes and Growth Factors Abstracts</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</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>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Family Health Database (ProQuest)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest research library</collection><collection>Research Library (Corporate)</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>MEDLINE - Academic</collection><jtitle>Breast cancer research and treatment</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhou, Ping</au><au>Du, Liang-Feng</au><au>Lv, Guo-Qiang</au><au>Yu, Xian-Ming</au><au>Gu, Yuan-Long</au><au>Li, Jian-Ping</au><au>Zhang, Chun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Current evidence on the relationship between four polymorphisms in the matrix metalloproteinases (MMP) gene and breast cancer risk: a meta-analysis</atitle><jtitle>Breast cancer research and treatment</jtitle><stitle>Breast Cancer Res Treat</stitle><addtitle>Breast Cancer Res Treat</addtitle><date>2011-06-01</date><risdate>2011</risdate><volume>127</volume><issue>3</issue><spage>813</spage><epage>818</epage><pages>813-818</pages><issn>0167-6806</issn><eissn>1573-7217</eissn><coden>BCTRD6</coden><abstract>The matrix metalloproteinases (MMP) can degrade various components of the extracellular matrix and its functional genetic polymorphisms may be associated with breast cancer risk. However, this relationship remains controversial. A meta-analysis was conducted in order to investigate the potential association between four polymorphisms in the MMP gene and breast cancer risk. A database search yielded a total of 9 studies involving 2,597 cases and 2,618 controls. Four polymorphisms were included in the meta-analysis: MMP-1 −1607 2G/1G (rs1799750), MMP-2 −1306 C/T (rs243865), MMP-3 −1171 6A/5A (rs3025058) and MMP-9 −1562 C/T (rs3918242). Crude odds ratios (OR) with 95% confidence intervals (CI) were used to assess the strength of association. When all the studies were pooled into the meta-analysis, we found that breast cancer cases had a significantly higher frequency of CC genotype (OR = 1.27, 95% CI = 1.10, 1.47;
P
= 0.001) and lower frequency of CT genotype (OR = 0.78, 95% CI = 0.67, 0.91;
P
= 0.001) of MMP-2. No significant difference was found in any genotype of MMP-1, MMP-3 or MMP-9. In conclusion, this meta-analysis suggested that MMP-2 −1306 C/T polymorphism may contribute to breast cancer susceptibility. More studies were needed especially in Asians in the future.</abstract><cop>Boston</cop><pub>Springer US</pub><pmid>21161369</pmid><doi>10.1007/s10549-010-1294-0</doi><tpages>6</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0167-6806 |
ispartof | Breast cancer research and treatment, 2011-06, Vol.127 (3), p.813-818 |
issn | 0167-6806 1573-7217 |
language | eng |
recordid | cdi_proquest_miscellaneous_868030764 |
source | Springer Nature |
subjects | Biological and medical sciences Breast cancer Breast Neoplasms - genetics Cancer Cancer research Epidemiology Female Genes Genetic aspects Genetic Association Studies Genetic Predisposition to Disease Genotype Gynecology. Andrology. Obstetrics Health aspects Humans Mammary gland diseases Matrix Metalloproteinases - genetics Medical sciences Medicine Medicine & Public Health Meta-analysis Odds Ratio Oncology Polymorphism Polymorphism, Single Nucleotide Promoter Regions, Genetic Risk Risk factors Tumors |
title | Current evidence on the relationship between four polymorphisms in the matrix metalloproteinases (MMP) gene and breast cancer risk: a meta-analysis |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T20%3A14%3A18IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Current%20evidence%20on%20the%20relationship%20between%20four%20polymorphisms%20in%20the%20matrix%20metalloproteinases%20(MMP)%20gene%20and%20breast%20cancer%20risk:%20a%20meta-analysis&rft.jtitle=Breast%20cancer%20research%20and%20treatment&rft.au=Zhou,%20Ping&rft.date=2011-06-01&rft.volume=127&rft.issue=3&rft.spage=813&rft.epage=818&rft.pages=813-818&rft.issn=0167-6806&rft.eissn=1573-7217&rft.coden=BCTRD6&rft_id=info:doi/10.1007/s10549-010-1294-0&rft_dat=%3Cgale_proqu%3EA356142747%3C/gale_proqu%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c498t-9d1f27f2716145af8d37cdac1f58059557040f21b0f0cbfe7896c5dd6d6863113%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=878132481&rft_id=info:pmid/21161369&rft_galeid=A356142747&rfr_iscdi=true |