A meta-analysis of microRNA expression in liver cancer
MicroRNA (miRNA) played an important role in the progression of liver cancer and its diagnostic and prognostic values have been frequently studied. However, different microarray techniques and small sample size led to inconsistent findings in previous studies. We performed a comprehensive meta-analy...
Gespeichert in:
Veröffentlicht in: | PloS one 2014-12, Vol.9 (12), p.e114533-e114533 |
---|---|
Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | e114533 |
---|---|
container_issue | 12 |
container_start_page | e114533 |
container_title | PloS one |
container_volume | 9 |
creator | Yang, Jingcheng Han, Shuai Huang, Wenwen Chen, Ting Liu, Yang Pan, Shangling Li, Shikang |
description | MicroRNA (miRNA) played an important role in the progression of liver cancer and its diagnostic and prognostic values have been frequently studied. However, different microarray techniques and small sample size led to inconsistent findings in previous studies. We performed a comprehensive meta-analysis of a total of 357 tumor and 283 noncancerous samples from 12 published miRNA expression studies using robust rank aggregation method. As a result, we identified a statistically significant meta-signature of five upregulated (miR-221, miR-222, miR-93, miR-21 and miR-224) and four downregulated (miR-130a, miR-195, miR-199a and miR-375) miRNAs. We then conducted miRNA target prediction and pathway enrichment analysis to find what biological process these miRNAs might affect. We found that most of the pathways were frequently associated with cell signaling and cancer pathogenesis. Thus these miRNAs may involve in the onset and progression of liver cancer and serve as potential diagnostic and therapeutic targets of this malignancy. |
doi_str_mv | 10.1371/journal.pone.0114533 |
format | Article |
fullrecord | <record><control><sourceid>gale_plos_</sourceid><recordid>TN_cdi_plos_journals_1635000385</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A418634401</galeid><doaj_id>oai_doaj_org_article_d5fbd45d3a7e460d887b855185e80869</doaj_id><sourcerecordid>A418634401</sourcerecordid><originalsourceid>FETCH-LOGICAL-c692t-39a40d7b7b8b4b715d0e9a2cf338ba26e7c6f82c5d4582ef9feedc05c0b699593</originalsourceid><addsrcrecordid>eNqNkk1r3DAQhk1padK0_6C0hkJpD95K1oelS2EJabsQGkg_rkKWx7tabGsj2SH595GzTliXHIoOEqNn3pmR3iR5i9ECkwJ_2brBd7pZ7FwHC4QxZYQ8S46xJHnGc0SeH5yPklchbBFiRHD-MjnKGZWIMXGc8GXaQq8zHaVugw2pq9PWGu8ufy5TuNl5CMG6LrVd2thr8KnRnQH_OnlR6ybAm2k_Sf58O_t9-iM7v_i-Ol2eZ4bLvM-I1BRVRVmUoqRlgVmFQOrc1ISIUuccCsNrkRtWUSZyqGUNUBnEDCq5lEySk-T9XnfXuKCmkYPCnDCEEBEsEqs9UTm9VTtvW-1vldNW3QecXyvte2saUBWry1ioIroAylElROyLMSwYCCT4WO3rVG0o29gIdL3XzUx0ftPZjVq7a0VzjgQVUeDTJODd1QChV60NBppGd-CG-74LKSlFI_rhH_Tp6SZqreMAtqtdrGtGUbWkWHAStXCkFk9QcVUQ_zL6o7YxPkv4PEuITA83_VoPIajVr8v_Zy_-ztmPB-wGdNNvgmuGPloozEG6B6PTQvBQPz4yRmq098NrqNHearJ3THt3-EGPSQ9-JndOUPLZ</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1635000385</pqid></control><display><type>article</type><title>A meta-analysis of microRNA expression in liver cancer</title><source>PubMed Central Free</source><source>MEDLINE</source><source>DOAJ Directory of Open Access Journals</source><source>Public Library of Science</source><source>Free Full-Text Journals in Chemistry</source><source>EZB Electronic Journals Library</source><creator>Yang, Jingcheng ; Han, Shuai ; Huang, Wenwen ; Chen, Ting ; Liu, Yang ; Pan, Shangling ; Li, Shikang</creator><contributor>Chemin, Isabelle A.</contributor><creatorcontrib>Yang, Jingcheng ; Han, Shuai ; Huang, Wenwen ; Chen, Ting ; Liu, Yang ; Pan, Shangling ; Li, Shikang ; Chemin, Isabelle A.</creatorcontrib><description>MicroRNA (miRNA) played an important role in the progression of liver cancer and its diagnostic and prognostic values have been frequently studied. However, different microarray techniques and small sample size led to inconsistent findings in previous studies. We performed a comprehensive meta-analysis of a total of 357 tumor and 283 noncancerous samples from 12 published miRNA expression studies using robust rank aggregation method. As a result, we identified a statistically significant meta-signature of five upregulated (miR-221, miR-222, miR-93, miR-21 and miR-224) and four downregulated (miR-130a, miR-195, miR-199a and miR-375) miRNAs. We then conducted miRNA target prediction and pathway enrichment analysis to find what biological process these miRNAs might affect. We found that most of the pathways were frequently associated with cell signaling and cancer pathogenesis. Thus these miRNAs may involve in the onset and progression of liver cancer and serve as potential diagnostic and therapeutic targets of this malignancy.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0114533</identifier><identifier>PMID: 25490558</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Biological activity ; Biology and life sciences ; Cancer ; Cluster Analysis ; Development and progression ; Diagnostic systems ; Gene Expression Profiling ; Humans ; Liver ; Liver cancer ; Liver Neoplasms - genetics ; Malignancy ; Medical diagnosis ; Medicine and Health Sciences ; Meta-analysis ; MicroRNA ; MicroRNAs - genetics ; miRNA ; Pathogenesis ; Ribonucleic acid ; RNA ; Statistical analysis ; Statistical methods ; Therapeutic applications</subject><ispartof>PloS one, 2014-12, Vol.9 (12), p.e114533-e114533</ispartof><rights>COPYRIGHT 2014 Public Library of Science</rights><rights>2014 Yang et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2014 Yang et al 2014 Yang et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-39a40d7b7b8b4b715d0e9a2cf338ba26e7c6f82c5d4582ef9feedc05c0b699593</citedby><cites>FETCH-LOGICAL-c692t-39a40d7b7b8b4b715d0e9a2cf338ba26e7c6f82c5d4582ef9feedc05c0b699593</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/PMC4260848/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4260848/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,728,781,785,865,886,2103,2929,23868,27926,27927,53793,53795</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25490558$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Chemin, Isabelle A.</contributor><creatorcontrib>Yang, Jingcheng</creatorcontrib><creatorcontrib>Han, Shuai</creatorcontrib><creatorcontrib>Huang, Wenwen</creatorcontrib><creatorcontrib>Chen, Ting</creatorcontrib><creatorcontrib>Liu, Yang</creatorcontrib><creatorcontrib>Pan, Shangling</creatorcontrib><creatorcontrib>Li, Shikang</creatorcontrib><title>A meta-analysis of microRNA expression in liver cancer</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>MicroRNA (miRNA) played an important role in the progression of liver cancer and its diagnostic and prognostic values have been frequently studied. However, different microarray techniques and small sample size led to inconsistent findings in previous studies. We performed a comprehensive meta-analysis of a total of 357 tumor and 283 noncancerous samples from 12 published miRNA expression studies using robust rank aggregation method. As a result, we identified a statistically significant meta-signature of five upregulated (miR-221, miR-222, miR-93, miR-21 and miR-224) and four downregulated (miR-130a, miR-195, miR-199a and miR-375) miRNAs. We then conducted miRNA target prediction and pathway enrichment analysis to find what biological process these miRNAs might affect. We found that most of the pathways were frequently associated with cell signaling and cancer pathogenesis. Thus these miRNAs may involve in the onset and progression of liver cancer and serve as potential diagnostic and therapeutic targets of this malignancy.</description><subject>Biological activity</subject><subject>Biology and life sciences</subject><subject>Cancer</subject><subject>Cluster Analysis</subject><subject>Development and progression</subject><subject>Diagnostic systems</subject><subject>Gene Expression Profiling</subject><subject>Humans</subject><subject>Liver</subject><subject>Liver cancer</subject><subject>Liver Neoplasms - genetics</subject><subject>Malignancy</subject><subject>Medical diagnosis</subject><subject>Medicine and Health Sciences</subject><subject>Meta-analysis</subject><subject>MicroRNA</subject><subject>MicroRNAs - genetics</subject><subject>miRNA</subject><subject>Pathogenesis</subject><subject>Ribonucleic acid</subject><subject>RNA</subject><subject>Statistical analysis</subject><subject>Statistical methods</subject><subject>Therapeutic applications</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</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><sourceid>GNUQQ</sourceid><sourceid>DOA</sourceid><recordid>eNqNkk1r3DAQhk1padK0_6C0hkJpD95K1oelS2EJabsQGkg_rkKWx7tabGsj2SH595GzTliXHIoOEqNn3pmR3iR5i9ECkwJ_2brBd7pZ7FwHC4QxZYQ8S46xJHnGc0SeH5yPklchbBFiRHD-MjnKGZWIMXGc8GXaQq8zHaVugw2pq9PWGu8ufy5TuNl5CMG6LrVd2thr8KnRnQH_OnlR6ybAm2k_Sf58O_t9-iM7v_i-Ol2eZ4bLvM-I1BRVRVmUoqRlgVmFQOrc1ISIUuccCsNrkRtWUSZyqGUNUBnEDCq5lEySk-T9XnfXuKCmkYPCnDCEEBEsEqs9UTm9VTtvW-1vldNW3QecXyvte2saUBWry1ioIroAylElROyLMSwYCCT4WO3rVG0o29gIdL3XzUx0ftPZjVq7a0VzjgQVUeDTJODd1QChV60NBppGd-CG-74LKSlFI_rhH_Tp6SZqreMAtqtdrGtGUbWkWHAStXCkFk9QcVUQ_zL6o7YxPkv4PEuITA83_VoPIajVr8v_Zy_-ztmPB-wGdNNvgmuGPloozEG6B6PTQvBQPz4yRmq098NrqNHearJ3THt3-EGPSQ9-JndOUPLZ</recordid><startdate>20141209</startdate><enddate>20141209</enddate><creator>Yang, Jingcheng</creator><creator>Han, Shuai</creator><creator>Huang, Wenwen</creator><creator>Chen, Ting</creator><creator>Liu, Yang</creator><creator>Pan, Shangling</creator><creator>Li, Shikang</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</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>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20141209</creationdate><title>A meta-analysis of microRNA expression in liver cancer</title><author>Yang, Jingcheng ; Han, Shuai ; Huang, Wenwen ; Chen, Ting ; Liu, Yang ; Pan, Shangling ; Li, Shikang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c692t-39a40d7b7b8b4b715d0e9a2cf338ba26e7c6f82c5d4582ef9feedc05c0b699593</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Biological activity</topic><topic>Biology and life sciences</topic><topic>Cancer</topic><topic>Cluster Analysis</topic><topic>Development and progression</topic><topic>Diagnostic systems</topic><topic>Gene Expression Profiling</topic><topic>Humans</topic><topic>Liver</topic><topic>Liver cancer</topic><topic>Liver Neoplasms - genetics</topic><topic>Malignancy</topic><topic>Medical diagnosis</topic><topic>Medicine and Health Sciences</topic><topic>Meta-analysis</topic><topic>MicroRNA</topic><topic>MicroRNAs - genetics</topic><topic>miRNA</topic><topic>Pathogenesis</topic><topic>Ribonucleic acid</topic><topic>RNA</topic><topic>Statistical analysis</topic><topic>Statistical methods</topic><topic>Therapeutic applications</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yang, Jingcheng</creatorcontrib><creatorcontrib>Han, Shuai</creatorcontrib><creatorcontrib>Huang, Wenwen</creatorcontrib><creatorcontrib>Chen, Ting</creatorcontrib><creatorcontrib>Liu, Yang</creatorcontrib><creatorcontrib>Pan, Shangling</creatorcontrib><creatorcontrib>Li, Shikang</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 : Opposing Viewpoints</collection><collection>Gale in Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Meteorological & Geoastrophysical Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</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>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies & Aerospace Database (1962 - current)</collection><collection>ProQuest Agriculture & Environmental Science Database</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Materials Science Database</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Meteorological & Geoastrophysical Abstracts - Academic</collection><collection>ProQuest Engineering Collection</collection><collection>Biological Sciences</collection><collection>Agriculture Science Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>ProQuest Biological Science Journals</collection><collection>ProQuest Engineering Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest Advanced Technologies & Aerospace Database</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>Materials science collection</collection><collection>Publicly Available Content Database</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>Engineering collection</collection><collection>Environmental Science Collection</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yang, Jingcheng</au><au>Han, Shuai</au><au>Huang, Wenwen</au><au>Chen, Ting</au><au>Liu, Yang</au><au>Pan, Shangling</au><au>Li, Shikang</au><au>Chemin, Isabelle A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A meta-analysis of microRNA expression in liver cancer</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2014-12-09</date><risdate>2014</risdate><volume>9</volume><issue>12</issue><spage>e114533</spage><epage>e114533</epage><pages>e114533-e114533</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>MicroRNA (miRNA) played an important role in the progression of liver cancer and its diagnostic and prognostic values have been frequently studied. However, different microarray techniques and small sample size led to inconsistent findings in previous studies. We performed a comprehensive meta-analysis of a total of 357 tumor and 283 noncancerous samples from 12 published miRNA expression studies using robust rank aggregation method. As a result, we identified a statistically significant meta-signature of five upregulated (miR-221, miR-222, miR-93, miR-21 and miR-224) and four downregulated (miR-130a, miR-195, miR-199a and miR-375) miRNAs. We then conducted miRNA target prediction and pathway enrichment analysis to find what biological process these miRNAs might affect. We found that most of the pathways were frequently associated with cell signaling and cancer pathogenesis. Thus these miRNAs may involve in the onset and progression of liver cancer and serve as potential diagnostic and therapeutic targets of this malignancy.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>25490558</pmid><doi>10.1371/journal.pone.0114533</doi><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1932-6203 |
ispartof | PloS one, 2014-12, Vol.9 (12), p.e114533-e114533 |
issn | 1932-6203 1932-6203 |
language | eng |
recordid | cdi_plos_journals_1635000385 |
source | PubMed Central Free; MEDLINE; DOAJ Directory of Open Access Journals; Public Library of Science; Free Full-Text Journals in Chemistry; EZB Electronic Journals Library |
subjects | Biological activity Biology and life sciences Cancer Cluster Analysis Development and progression Diagnostic systems Gene Expression Profiling Humans Liver Liver cancer Liver Neoplasms - genetics Malignancy Medical diagnosis Medicine and Health Sciences Meta-analysis MicroRNA MicroRNAs - genetics miRNA Pathogenesis Ribonucleic acid RNA Statistical analysis Statistical methods Therapeutic applications |
title | A meta-analysis of microRNA expression in liver cancer |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-17T20%3A34%3A09IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20meta-analysis%20of%20microRNA%20expression%20in%20liver%20cancer&rft.jtitle=PloS%20one&rft.au=Yang,%20Jingcheng&rft.date=2014-12-09&rft.volume=9&rft.issue=12&rft.spage=e114533&rft.epage=e114533&rft.pages=e114533-e114533&rft.issn=1932-6203&rft.eissn=1932-6203&rft_id=info:doi/10.1371/journal.pone.0114533&rft_dat=%3Cgale_plos_%3EA418634401%3C/gale_plos_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1635000385&rft_id=info:pmid/25490558&rft_galeid=A418634401&rft_doaj_id=oai_doaj_org_article_d5fbd45d3a7e460d887b855185e80869&rfr_iscdi=true |