Panels of circulating microRNAs as potential diagnostic biomarkers for breast cancer: a systematic review and meta-analysis
Purpose Circulating microRNAs (miRNAs) are potential diagnostic biomarkers for breast cancer (BC). The application of miRNA panels could improve the performance of screening tests. Here, we integrated bioinformatic tools and meta-analyses to select circulating miRNAs with high diagnostic accuracy an...
Gespeichert in:
Veröffentlicht in: | Breast cancer research and treatment 2022-11, Vol.196 (1), p.1-15 |
---|---|
Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 15 |
---|---|
container_issue | 1 |
container_start_page | 1 |
container_title | Breast cancer research and treatment |
container_volume | 196 |
creator | Nguyen, Thu H. N. Nguyen, Thanh T. N. Nguyen, Tran T. M. Nguyen, Le H. M. Huynh, Luan H. Phan, Hoang N. Nguyen, Hue T. |
description | Purpose
Circulating microRNAs (miRNAs) are potential diagnostic biomarkers for breast cancer (BC). The application of miRNA panels could improve the performance of screening tests. Here, we integrated bioinformatic tools and meta-analyses to select circulating miRNAs with high diagnostic accuracy and combined these markers to develop diagnostic panels for BC.
Methods
Analyses across databases were performed to identify potential BC-related circulating miRNAs. Next, a comprehensive meta-analysis was conducted for each miRNA following the PRISMA guidelines. An electronic and manual search for relevant literature was carried out by two reviewers through PubMed, ScienceDirect, Biomed Central, and Google Scholar. The quality of the included studies was assessed using the QUADAS-2, and the statistical analyses were performed using R software 4.1.1. Finally, the accurate biomarkers confirmed through meta-analyses were combined into diagnostic models for BC.
Results
Twenty-seven circulating miRNAs were identified as BC-related by bioinformatic tools. After screening, only 10 miRNAs presented in 45 studies were eligible for meta-analyses. By assessing pooled sensitivity, specificity, positive likelihood ratio, negative likelihood ratio, and diagnostic odds ratio, 8 miRNAs (miR-21, miR-30b, miR-125b, miR-145, miR221 miR-222, and miR-335) were revealed as promising BC diagnostic biomarkers. Two panels constructed from these miRNAs showed excellent diagnostic accuracy for BC, with areas under the SROC curve of 0.917 and 0.944.
Conclusion
We identified 8 potential circulating miRNAs and 2 diagnostic models that are useful for diagnosing BC. However, the established miRNA panels have not been tested in any experimental studies and thus should be validated in large case–control studies for clinical use. |
doi_str_mv | 10.1007/s10549-022-06728-8 |
format | Article |
fullrecord | <record><control><sourceid>gale_proqu</sourceid><recordid>TN_cdi_proquest_miscellaneous_2712849268</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A721987853</galeid><sourcerecordid>A721987853</sourcerecordid><originalsourceid>FETCH-LOGICAL-c516t-aed4847e5d3b5f364f91f120d918f7c3a00e3cd0247ceb35edaf6410c24f7eb53</originalsourceid><addsrcrecordid>eNp9kluLFDEQhRtRcFz9Az4FBPGl1yR9Sbdvw-INFhXR51CdrsxmzSRjKq0M_nnTjrCuiNRDoPhOkVN1quqx4OeCc_WcBO_aseZS1rxXcqiHO9VGdKqplRTqbrXhold1P_D-fvWA6JpzPio-bqofHyCgJxYtMy6ZxUN2Ycf2zqT48d2WGBA7xIwhO_BsdrALkbIzbHJxD-kLJmI2JjYlBMrMQDCYXjBgdKSMe1jRhN8cfmcQZrbHDDUE8Edy9LC6Z8ETPvr9nlWfX738dPGmvnz_-u3F9rI2nehzDTi3Q6uwm5ups03f2lFYIfk8isEq0wDn2JiZy1YZnJoOZ7B9K7iRrVU4dc1Z9ew095Di1wUp670jg94X63EhLZWQQzvKfijok7_Q67ik8t-Vko0cZCfaG2oHHrULNuYEZh2qt2Xf46CGrinU-T-oUjOW9caA1pX-LcHTPwRXCD5fUfRLdjHQbVCewHIkooRWH5Ir1zhqwfWaB33Kgy550L_yoFdrzUlEBQ47TDfW_qP6CX7Ut9A</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2723282514</pqid></control><display><type>article</type><title>Panels of circulating microRNAs as potential diagnostic biomarkers for breast cancer: a systematic review and meta-analysis</title><source>Springer Nature - Complete Springer Journals</source><creator>Nguyen, Thu H. N. ; Nguyen, Thanh T. N. ; Nguyen, Tran T. M. ; Nguyen, Le H. M. ; Huynh, Luan H. ; Phan, Hoang N. ; Nguyen, Hue T.</creator><creatorcontrib>Nguyen, Thu H. N. ; Nguyen, Thanh T. N. ; Nguyen, Tran T. M. ; Nguyen, Le H. M. ; Huynh, Luan H. ; Phan, Hoang N. ; Nguyen, Hue T.</creatorcontrib><description>Purpose
Circulating microRNAs (miRNAs) are potential diagnostic biomarkers for breast cancer (BC). The application of miRNA panels could improve the performance of screening tests. Here, we integrated bioinformatic tools and meta-analyses to select circulating miRNAs with high diagnostic accuracy and combined these markers to develop diagnostic panels for BC.
Methods
Analyses across databases were performed to identify potential BC-related circulating miRNAs. Next, a comprehensive meta-analysis was conducted for each miRNA following the PRISMA guidelines. An electronic and manual search for relevant literature was carried out by two reviewers through PubMed, ScienceDirect, Biomed Central, and Google Scholar. The quality of the included studies was assessed using the QUADAS-2, and the statistical analyses were performed using R software 4.1.1. Finally, the accurate biomarkers confirmed through meta-analyses were combined into diagnostic models for BC.
Results
Twenty-seven circulating miRNAs were identified as BC-related by bioinformatic tools. After screening, only 10 miRNAs presented in 45 studies were eligible for meta-analyses. By assessing pooled sensitivity, specificity, positive likelihood ratio, negative likelihood ratio, and diagnostic odds ratio, 8 miRNAs (miR-21, miR-30b, miR-125b, miR-145, miR221 miR-222, and miR-335) were revealed as promising BC diagnostic biomarkers. Two panels constructed from these miRNAs showed excellent diagnostic accuracy for BC, with areas under the SROC curve of 0.917 and 0.944.
Conclusion
We identified 8 potential circulating miRNAs and 2 diagnostic models that are useful for diagnosing BC. However, the established miRNA panels have not been tested in any experimental studies and thus should be validated in large case–control studies for clinical use.</description><identifier>ISSN: 0167-6806</identifier><identifier>EISSN: 1573-7217</identifier><identifier>DOI: 10.1007/s10549-022-06728-8</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Biological markers ; Biomarkers ; Breast cancer ; Cancer research ; Medical screening ; Medicine ; Medicine & Public Health ; Meta-analysis ; MicroRNA ; MicroRNAs ; miRNA ; Oncology ; Review ; Statistical analysis</subject><ispartof>Breast cancer research and treatment, 2022-11, Vol.196 (1), p.1-15</ispartof><rights>The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2022. Springer Nature or its licensor holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><rights>COPYRIGHT 2022 Springer</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c516t-aed4847e5d3b5f364f91f120d918f7c3a00e3cd0247ceb35edaf6410c24f7eb53</citedby><cites>FETCH-LOGICAL-c516t-aed4847e5d3b5f364f91f120d918f7c3a00e3cd0247ceb35edaf6410c24f7eb53</cites><orcidid>0000-0001-7097-7608</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10549-022-06728-8$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10549-022-06728-8$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids></links><search><creatorcontrib>Nguyen, Thu H. N.</creatorcontrib><creatorcontrib>Nguyen, Thanh T. N.</creatorcontrib><creatorcontrib>Nguyen, Tran T. M.</creatorcontrib><creatorcontrib>Nguyen, Le H. M.</creatorcontrib><creatorcontrib>Huynh, Luan H.</creatorcontrib><creatorcontrib>Phan, Hoang N.</creatorcontrib><creatorcontrib>Nguyen, Hue T.</creatorcontrib><title>Panels of circulating microRNAs as potential diagnostic biomarkers for breast cancer: a systematic review and meta-analysis</title><title>Breast cancer research and treatment</title><addtitle>Breast Cancer Res Treat</addtitle><description>Purpose
Circulating microRNAs (miRNAs) are potential diagnostic biomarkers for breast cancer (BC). The application of miRNA panels could improve the performance of screening tests. Here, we integrated bioinformatic tools and meta-analyses to select circulating miRNAs with high diagnostic accuracy and combined these markers to develop diagnostic panels for BC.
Methods
Analyses across databases were performed to identify potential BC-related circulating miRNAs. Next, a comprehensive meta-analysis was conducted for each miRNA following the PRISMA guidelines. An electronic and manual search for relevant literature was carried out by two reviewers through PubMed, ScienceDirect, Biomed Central, and Google Scholar. The quality of the included studies was assessed using the QUADAS-2, and the statistical analyses were performed using R software 4.1.1. Finally, the accurate biomarkers confirmed through meta-analyses were combined into diagnostic models for BC.
Results
Twenty-seven circulating miRNAs were identified as BC-related by bioinformatic tools. After screening, only 10 miRNAs presented in 45 studies were eligible for meta-analyses. By assessing pooled sensitivity, specificity, positive likelihood ratio, negative likelihood ratio, and diagnostic odds ratio, 8 miRNAs (miR-21, miR-30b, miR-125b, miR-145, miR221 miR-222, and miR-335) were revealed as promising BC diagnostic biomarkers. Two panels constructed from these miRNAs showed excellent diagnostic accuracy for BC, with areas under the SROC curve of 0.917 and 0.944.
Conclusion
We identified 8 potential circulating miRNAs and 2 diagnostic models that are useful for diagnosing BC. However, the established miRNA panels have not been tested in any experimental studies and thus should be validated in large case–control studies for clinical use.</description><subject>Biological markers</subject><subject>Biomarkers</subject><subject>Breast cancer</subject><subject>Cancer research</subject><subject>Medical screening</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Meta-analysis</subject><subject>MicroRNA</subject><subject>MicroRNAs</subject><subject>miRNA</subject><subject>Oncology</subject><subject>Review</subject><subject>Statistical analysis</subject><issn>0167-6806</issn><issn>1573-7217</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNp9kluLFDEQhRtRcFz9Az4FBPGl1yR9Sbdvw-INFhXR51CdrsxmzSRjKq0M_nnTjrCuiNRDoPhOkVN1quqx4OeCc_WcBO_aseZS1rxXcqiHO9VGdKqplRTqbrXhold1P_D-fvWA6JpzPio-bqofHyCgJxYtMy6ZxUN2Ycf2zqT48d2WGBA7xIwhO_BsdrALkbIzbHJxD-kLJmI2JjYlBMrMQDCYXjBgdKSMe1jRhN8cfmcQZrbHDDUE8Edy9LC6Z8ETPvr9nlWfX738dPGmvnz_-u3F9rI2nehzDTi3Q6uwm5ups03f2lFYIfk8isEq0wDn2JiZy1YZnJoOZ7B9K7iRrVU4dc1Z9ew095Di1wUp670jg94X63EhLZWQQzvKfijok7_Q67ik8t-Vko0cZCfaG2oHHrULNuYEZh2qt2Xf46CGrinU-T-oUjOW9caA1pX-LcHTPwRXCD5fUfRLdjHQbVCewHIkooRWH5Ir1zhqwfWaB33Kgy550L_yoFdrzUlEBQ47TDfW_qP6CX7Ut9A</recordid><startdate>20221101</startdate><enddate>20221101</enddate><creator>Nguyen, Thu H. N.</creator><creator>Nguyen, Thanh T. N.</creator><creator>Nguyen, Tran T. M.</creator><creator>Nguyen, Le H. M.</creator><creator>Huynh, Luan H.</creator><creator>Phan, Hoang N.</creator><creator>Nguyen, Hue T.</creator><general>Springer US</general><general>Springer</general><general>Springer Nature B.V</general><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><orcidid>https://orcid.org/0000-0001-7097-7608</orcidid></search><sort><creationdate>20221101</creationdate><title>Panels of circulating microRNAs as potential diagnostic biomarkers for breast cancer: a systematic review and meta-analysis</title><author>Nguyen, Thu H. N. ; Nguyen, Thanh T. N. ; Nguyen, Tran T. M. ; Nguyen, Le H. M. ; Huynh, Luan H. ; Phan, Hoang N. ; Nguyen, Hue T.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c516t-aed4847e5d3b5f364f91f120d918f7c3a00e3cd0247ceb35edaf6410c24f7eb53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Biological markers</topic><topic>Biomarkers</topic><topic>Breast cancer</topic><topic>Cancer research</topic><topic>Medical screening</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Meta-analysis</topic><topic>MicroRNA</topic><topic>MicroRNAs</topic><topic>miRNA</topic><topic>Oncology</topic><topic>Review</topic><topic>Statistical analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nguyen, Thu H. N.</creatorcontrib><creatorcontrib>Nguyen, Thanh T. N.</creatorcontrib><creatorcontrib>Nguyen, Tran T. M.</creatorcontrib><creatorcontrib>Nguyen, Le H. M.</creatorcontrib><creatorcontrib>Huynh, Luan H.</creatorcontrib><creatorcontrib>Phan, Hoang N.</creatorcontrib><creatorcontrib>Nguyen, Hue T.</creatorcontrib><collection>CrossRef</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>ProQuest Pharma Collection</collection><collection>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 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>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>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>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>Nguyen, Thu H. N.</au><au>Nguyen, Thanh T. N.</au><au>Nguyen, Tran T. M.</au><au>Nguyen, Le H. M.</au><au>Huynh, Luan H.</au><au>Phan, Hoang N.</au><au>Nguyen, Hue T.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Panels of circulating microRNAs as potential diagnostic biomarkers for breast cancer: a systematic review and meta-analysis</atitle><jtitle>Breast cancer research and treatment</jtitle><stitle>Breast Cancer Res Treat</stitle><date>2022-11-01</date><risdate>2022</risdate><volume>196</volume><issue>1</issue><spage>1</spage><epage>15</epage><pages>1-15</pages><issn>0167-6806</issn><eissn>1573-7217</eissn><abstract>Purpose
Circulating microRNAs (miRNAs) are potential diagnostic biomarkers for breast cancer (BC). The application of miRNA panels could improve the performance of screening tests. Here, we integrated bioinformatic tools and meta-analyses to select circulating miRNAs with high diagnostic accuracy and combined these markers to develop diagnostic panels for BC.
Methods
Analyses across databases were performed to identify potential BC-related circulating miRNAs. Next, a comprehensive meta-analysis was conducted for each miRNA following the PRISMA guidelines. An electronic and manual search for relevant literature was carried out by two reviewers through PubMed, ScienceDirect, Biomed Central, and Google Scholar. The quality of the included studies was assessed using the QUADAS-2, and the statistical analyses were performed using R software 4.1.1. Finally, the accurate biomarkers confirmed through meta-analyses were combined into diagnostic models for BC.
Results
Twenty-seven circulating miRNAs were identified as BC-related by bioinformatic tools. After screening, only 10 miRNAs presented in 45 studies were eligible for meta-analyses. By assessing pooled sensitivity, specificity, positive likelihood ratio, negative likelihood ratio, and diagnostic odds ratio, 8 miRNAs (miR-21, miR-30b, miR-125b, miR-145, miR221 miR-222, and miR-335) were revealed as promising BC diagnostic biomarkers. Two panels constructed from these miRNAs showed excellent diagnostic accuracy for BC, with areas under the SROC curve of 0.917 and 0.944.
Conclusion
We identified 8 potential circulating miRNAs and 2 diagnostic models that are useful for diagnosing BC. However, the established miRNA panels have not been tested in any experimental studies and thus should be validated in large case–control studies for clinical use.</abstract><cop>New York</cop><pub>Springer US</pub><doi>10.1007/s10549-022-06728-8</doi><tpages>15</tpages><orcidid>https://orcid.org/0000-0001-7097-7608</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0167-6806 |
ispartof | Breast cancer research and treatment, 2022-11, Vol.196 (1), p.1-15 |
issn | 0167-6806 1573-7217 |
language | eng |
recordid | cdi_proquest_miscellaneous_2712849268 |
source | Springer Nature - Complete Springer Journals |
subjects | Biological markers Biomarkers Breast cancer Cancer research Medical screening Medicine Medicine & Public Health Meta-analysis MicroRNA MicroRNAs miRNA Oncology Review Statistical analysis |
title | Panels of circulating microRNAs as potential diagnostic biomarkers for breast cancer: a systematic review and meta-analysis |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-31T17%3A58%3A56IST&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=Panels%20of%20circulating%20microRNAs%20as%20potential%20diagnostic%20biomarkers%20for%20breast%20cancer:%20a%20systematic%20review%20and%20meta-analysis&rft.jtitle=Breast%20cancer%20research%20and%20treatment&rft.au=Nguyen,%20Thu%20H.%20N.&rft.date=2022-11-01&rft.volume=196&rft.issue=1&rft.spage=1&rft.epage=15&rft.pages=1-15&rft.issn=0167-6806&rft.eissn=1573-7217&rft_id=info:doi/10.1007/s10549-022-06728-8&rft_dat=%3Cgale_proqu%3EA721987853%3C/gale_proqu%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2723282514&rft_id=info:pmid/&rft_galeid=A721987853&rfr_iscdi=true |