Frequent down-regulation of ABC transporter genes in prostate cancer
ATP-binding cassette (ABC) transporters are transmembrane proteins responsible for the efflux of a wide variety of substrates, including steroid metabolites, through the cellular membranes. For better characterization of the role of ABC transporters in prostate cancer (PCa) development, the profile...
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description | ATP-binding cassette (ABC) transporters are transmembrane proteins responsible for the efflux of a wide variety of substrates, including steroid metabolites, through the cellular membranes. For better characterization of the role of ABC transporters in prostate cancer (PCa) development, the profile of ABC transporter gene expression was analyzed in PCa and noncancerous prostate tissues (NPT).
TaqMan Low Density Array (TLDA) human ABC transporter plates were used for the gene expression profiling in 10 PCa and 6 NPT specimens. ABCB1 transcript level was evaluated in a larger set of PCa cases (N = 78) and NPT (N = 15) by real-time PCR, the same PCa cases were assessed for the gene promoter hypermethylation by methylation-specific PCR.
Expression of eight ABC transporter genes (ABCA8, ABCB1, ABCC6, ABCC9, ABCC10, ABCD2, ABCG2, and ABCG4) was significantly down-regulated in PCa as compared to NPT, and only two genes (ABCC4 and ABCG1) were up-regulated. Down-regulation of ABC transporter genes was prevalent in the TMPRSS2-ERG-negative cases. A detailed analysis of ABCB1 expression confirmed TLDA results: a reduced level of the transcript was identified in PCa in comparison to NPT (p = 0.048). Moreover, the TMPRSS2-ERG-negative PCa cases showed significantly lower expression of ABCB1 in comparison to NPT (p = 0.003) or the fusion-positive tumors (p = 0.002). Promoter methylation of ABCB1 predominantly occurred in PCa and was rarely detected in NPT (p |
doi_str_mv | 10.1186/s12885-015-1689-8 |
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TaqMan Low Density Array (TLDA) human ABC transporter plates were used for the gene expression profiling in 10 PCa and 6 NPT specimens. ABCB1 transcript level was evaluated in a larger set of PCa cases (N = 78) and NPT (N = 15) by real-time PCR, the same PCa cases were assessed for the gene promoter hypermethylation by methylation-specific PCR.
Expression of eight ABC transporter genes (ABCA8, ABCB1, ABCC6, ABCC9, ABCC10, ABCD2, ABCG2, and ABCG4) was significantly down-regulated in PCa as compared to NPT, and only two genes (ABCC4 and ABCG1) were up-regulated. Down-regulation of ABC transporter genes was prevalent in the TMPRSS2-ERG-negative cases. A detailed analysis of ABCB1 expression confirmed TLDA results: a reduced level of the transcript was identified in PCa in comparison to NPT (p = 0.048). Moreover, the TMPRSS2-ERG-negative PCa cases showed significantly lower expression of ABCB1 in comparison to NPT (p = 0.003) or the fusion-positive tumors (p = 0.002). Promoter methylation of ABCB1 predominantly occurred in PCa and was rarely detected in NPT (p < 0.001).
The study suggests frequent down-regulation of the ABC transporter genes in PCa, especially in the TMPRSS2-ERG-negative tumors.</description><identifier>ISSN: 1471-2407</identifier><identifier>EISSN: 1471-2407</identifier><identifier>DOI: 10.1186/s12885-015-1689-8</identifier><identifier>PMID: 26459268</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>ABC transporters ; Analysis ; Androgens ; ATP Binding Cassette Transporter, Sub-Family B - genetics ; ATP-Binding Cassette Transporters - genetics ; Cancer ; Cancer therapies ; Cluster Analysis ; CpG Islands ; DNA Methylation ; Down-Regulation ; Gene expression ; Gene Expression Profiling ; Gene Expression Regulation, Neoplastic ; Genes ; Genetic aspects ; Genetic research ; Humans ; Male ; Membrane proteins ; Metabolites ; Methylation ; Multigene Family ; Neoplasm Grading ; Neoplasm Staging ; Prostate cancer ; Prostatic Neoplasms - genetics ; Prostatic Neoplasms - pathology ; Steroids ; Thermal cycling ; Transcription Initiation Site ; Tumors</subject><ispartof>BMC cancer, 2015-10, Vol.15 (1), p.683-683, Article 683</ispartof><rights>COPYRIGHT 2015 BioMed Central Ltd.</rights><rights>Copyright BioMed Central 2015</rights><rights>Demidenko et al. 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c625t-84f5cd7093ef425d21b719d24d77d6a3a788795d8c821c2d4503a6bbd996ff6d3</citedby><cites>FETCH-LOGICAL-c625t-84f5cd7093ef425d21b719d24d77d6a3a788795d8c821c2d4503a6bbd996ff6d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4603841/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4603841/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26459268$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Demidenko, Rita</creatorcontrib><creatorcontrib>Razanauskas, Deividas</creatorcontrib><creatorcontrib>Daniunaite, Kristina</creatorcontrib><creatorcontrib>Lazutka, Juozas Rimantas</creatorcontrib><creatorcontrib>Jankevicius, Feliksas</creatorcontrib><creatorcontrib>Jarmalaite, Sonata</creatorcontrib><title>Frequent down-regulation of ABC transporter genes in prostate cancer</title><title>BMC cancer</title><addtitle>BMC Cancer</addtitle><description>ATP-binding cassette (ABC) transporters are transmembrane proteins responsible for the efflux of a wide variety of substrates, including steroid metabolites, through the cellular membranes. For better characterization of the role of ABC transporters in prostate cancer (PCa) development, the profile of ABC transporter gene expression was analyzed in PCa and noncancerous prostate tissues (NPT).
TaqMan Low Density Array (TLDA) human ABC transporter plates were used for the gene expression profiling in 10 PCa and 6 NPT specimens. ABCB1 transcript level was evaluated in a larger set of PCa cases (N = 78) and NPT (N = 15) by real-time PCR, the same PCa cases were assessed for the gene promoter hypermethylation by methylation-specific PCR.
Expression of eight ABC transporter genes (ABCA8, ABCB1, ABCC6, ABCC9, ABCC10, ABCD2, ABCG2, and ABCG4) was significantly down-regulated in PCa as compared to NPT, and only two genes (ABCC4 and ABCG1) were up-regulated. Down-regulation of ABC transporter genes was prevalent in the TMPRSS2-ERG-negative cases. A detailed analysis of ABCB1 expression confirmed TLDA results: a reduced level of the transcript was identified in PCa in comparison to NPT (p = 0.048). Moreover, the TMPRSS2-ERG-negative PCa cases showed significantly lower expression of ABCB1 in comparison to NPT (p = 0.003) or the fusion-positive tumors (p = 0.002). Promoter methylation of ABCB1 predominantly occurred in PCa and was rarely detected in NPT (p < 0.001).
The study suggests frequent down-regulation of the ABC transporter genes in PCa, especially in the TMPRSS2-ERG-negative tumors.</description><subject>ABC transporters</subject><subject>Analysis</subject><subject>Androgens</subject><subject>ATP Binding Cassette Transporter, Sub-Family B - genetics</subject><subject>ATP-Binding Cassette Transporters - genetics</subject><subject>Cancer</subject><subject>Cancer therapies</subject><subject>Cluster Analysis</subject><subject>CpG Islands</subject><subject>DNA Methylation</subject><subject>Down-Regulation</subject><subject>Gene expression</subject><subject>Gene Expression Profiling</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Genes</subject><subject>Genetic aspects</subject><subject>Genetic research</subject><subject>Humans</subject><subject>Male</subject><subject>Membrane proteins</subject><subject>Metabolites</subject><subject>Methylation</subject><subject>Multigene Family</subject><subject>Neoplasm Grading</subject><subject>Neoplasm Staging</subject><subject>Prostate cancer</subject><subject>Prostatic Neoplasms - genetics</subject><subject>Prostatic Neoplasms - pathology</subject><subject>Steroids</subject><subject>Thermal cycling</subject><subject>Transcription Initiation Site</subject><subject>Tumors</subject><issn>1471-2407</issn><issn>1471-2407</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNptkl1rFDEUhoNYbK3-AG9kQBC9mJpk8jU3wna1tVAQ_LgO2eTM7JTZZJtkqv57s2ytOyK5SEie903OyYvQC4LPCFHiXSJUKV5jwmsiVFurR-iEMElqyrB8fLA-Rk9TusGYSIXVE3RMBeMtFeoEfbiIcDuBz5ULP3wdoZ9Gk4fgq9BVi_NllaPxaRtihlj14CFVg6-2MaRsMlTWeAvxGTrqzJjg-f18ir5ffPy2_FRff768Wi6uaysoz7ViHbdO4raBjlHuKFlJ0jrKnJROmMZIpWTLnbKKEksd47gxYrVybSu6TrjmFL3f-26n1QacLc-OZtTbOGxM_KWDGfT8xA9r3Yc7zQRuFCPF4M29QQyl6pT1ZkgWxtF4CFPSRFJaGis5L-irf9CbMEVfyiuUbBVlqsF_qd6MoAffhXKv3ZnqBWeEYUq5KNTZf6gyHGwGGzx0Q9mfCd7OBIXJ8DP3ZkpJX339MmdfH7BrMGNepzBOu09Mc5DsQVt-L0XoHhpHsN7lSe_zpEue9C5PWhXNy8OOPyj-BKj5DdHGwok</recordid><startdate>20151012</startdate><enddate>20151012</enddate><creator>Demidenko, Rita</creator><creator>Razanauskas, Deividas</creator><creator>Daniunaite, Kristina</creator><creator>Lazutka, Juozas Rimantas</creator><creator>Jankevicius, Feliksas</creator><creator>Jarmalaite, Sonata</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><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>ISR</scope><scope>3V.</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</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>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20151012</creationdate><title>Frequent down-regulation of ABC transporter genes in prostate cancer</title><author>Demidenko, Rita ; Razanauskas, Deividas ; Daniunaite, Kristina ; Lazutka, Juozas Rimantas ; Jankevicius, Feliksas ; Jarmalaite, Sonata</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c625t-84f5cd7093ef425d21b719d24d77d6a3a788795d8c821c2d4503a6bbd996ff6d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>ABC transporters</topic><topic>Analysis</topic><topic>Androgens</topic><topic>ATP Binding Cassette Transporter, Sub-Family B - genetics</topic><topic>ATP-Binding Cassette Transporters - genetics</topic><topic>Cancer</topic><topic>Cancer therapies</topic><topic>Cluster Analysis</topic><topic>CpG Islands</topic><topic>DNA Methylation</topic><topic>Down-Regulation</topic><topic>Gene expression</topic><topic>Gene Expression Profiling</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Genes</topic><topic>Genetic aspects</topic><topic>Genetic research</topic><topic>Humans</topic><topic>Male</topic><topic>Membrane proteins</topic><topic>Metabolites</topic><topic>Methylation</topic><topic>Multigene Family</topic><topic>Neoplasm Grading</topic><topic>Neoplasm Staging</topic><topic>Prostate cancer</topic><topic>Prostatic Neoplasms - genetics</topic><topic>Prostatic Neoplasms - pathology</topic><topic>Steroids</topic><topic>Thermal cycling</topic><topic>Transcription Initiation Site</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Demidenko, Rita</creatorcontrib><creatorcontrib>Razanauskas, Deividas</creatorcontrib><creatorcontrib>Daniunaite, Kristina</creatorcontrib><creatorcontrib>Lazutka, Juozas Rimantas</creatorcontrib><creatorcontrib>Jankevicius, Feliksas</creatorcontrib><creatorcontrib>Jarmalaite, Sonata</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</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 Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Access via ProQuest (Open Access)</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>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>BMC cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Demidenko, Rita</au><au>Razanauskas, Deividas</au><au>Daniunaite, Kristina</au><au>Lazutka, Juozas Rimantas</au><au>Jankevicius, Feliksas</au><au>Jarmalaite, Sonata</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Frequent down-regulation of ABC transporter genes in prostate cancer</atitle><jtitle>BMC cancer</jtitle><addtitle>BMC Cancer</addtitle><date>2015-10-12</date><risdate>2015</risdate><volume>15</volume><issue>1</issue><spage>683</spage><epage>683</epage><pages>683-683</pages><artnum>683</artnum><issn>1471-2407</issn><eissn>1471-2407</eissn><abstract>ATP-binding cassette (ABC) transporters are transmembrane proteins responsible for the efflux of a wide variety of substrates, including steroid metabolites, through the cellular membranes. For better characterization of the role of ABC transporters in prostate cancer (PCa) development, the profile of ABC transporter gene expression was analyzed in PCa and noncancerous prostate tissues (NPT).
TaqMan Low Density Array (TLDA) human ABC transporter plates were used for the gene expression profiling in 10 PCa and 6 NPT specimens. ABCB1 transcript level was evaluated in a larger set of PCa cases (N = 78) and NPT (N = 15) by real-time PCR, the same PCa cases were assessed for the gene promoter hypermethylation by methylation-specific PCR.
Expression of eight ABC transporter genes (ABCA8, ABCB1, ABCC6, ABCC9, ABCC10, ABCD2, ABCG2, and ABCG4) was significantly down-regulated in PCa as compared to NPT, and only two genes (ABCC4 and ABCG1) were up-regulated. Down-regulation of ABC transporter genes was prevalent in the TMPRSS2-ERG-negative cases. A detailed analysis of ABCB1 expression confirmed TLDA results: a reduced level of the transcript was identified in PCa in comparison to NPT (p = 0.048). Moreover, the TMPRSS2-ERG-negative PCa cases showed significantly lower expression of ABCB1 in comparison to NPT (p = 0.003) or the fusion-positive tumors (p = 0.002). Promoter methylation of ABCB1 predominantly occurred in PCa and was rarely detected in NPT (p < 0.001).
The study suggests frequent down-regulation of the ABC transporter genes in PCa, especially in the TMPRSS2-ERG-negative tumors.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>26459268</pmid><doi>10.1186/s12885-015-1689-8</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | ABC transporters Analysis Androgens ATP Binding Cassette Transporter, Sub-Family B - genetics ATP-Binding Cassette Transporters - genetics Cancer Cancer therapies Cluster Analysis CpG Islands DNA Methylation Down-Regulation Gene expression Gene Expression Profiling Gene Expression Regulation, Neoplastic Genes Genetic aspects Genetic research Humans Male Membrane proteins Metabolites Methylation Multigene Family Neoplasm Grading Neoplasm Staging Prostate cancer Prostatic Neoplasms - genetics Prostatic Neoplasms - pathology Steroids Thermal cycling Transcription Initiation Site Tumors |
title | Frequent down-regulation of ABC transporter genes in prostate cancer |
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