Key pathways involved in prostate cancer based on gene set enrichment analysis and meta analysis

Prostate cancer is one of the most common male malignant neoplasms; however, its causes are not completely understood. A few recent studies have used gene expression profiling of prostate cancer to identify differentially expressed genes and possible relevant pathways. However, few studies have exam...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Genetics and molecular research 2011-12, Vol.10 (4), p.3856-3887
Hauptverfasser: Ning, Q Y, Wu, J Z, Zang, N, Liang, J, Hu, Y L, Mo, Z N
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 3887
container_issue 4
container_start_page 3856
container_title Genetics and molecular research
container_volume 10
creator Ning, Q Y
Wu, J Z
Zang, N
Liang, J
Hu, Y L
Mo, Z N
description Prostate cancer is one of the most common male malignant neoplasms; however, its causes are not completely understood. A few recent studies have used gene expression profiling of prostate cancer to identify differentially expressed genes and possible relevant pathways. However, few studies have examined the genetic mechanics of prostate cancer at the pathway level to search for such pathways. We used gene set enrichment analysis and a meta-analysis of six independent studies after standardized microarray preprocessing, which increased concordance between these gene datasets. Based on gene set enrichment analysis, there were 12 down- and 25 up-regulated mixing pathways in more than two tissue datasets, while there were two down- and two up-regulated mixing pathways in three cell datasets. Based on the meta-analysis, there were 46 and nine common pathways in the tissue and cell datasets, respectively. Three up- and 10 down-regulated crossing pathways were detected with combined gene set enrichment analysis and meta-analysis. We found that genes with small changes are difficult to detect by classic univariate statistics; they can more easily be identified by pathway analysis. After standardized microarray preprocessing, we applied gene set enrichment analysis and a meta-analysis to increase the concordance in identifying biological mechanisms involved in prostate cancer. The gene pathways that we identified could provide insight concerning the development of prostate cancer.
doi_str_mv 10.4238/2011.December.14.10
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1012745838</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1012745838</sourcerecordid><originalsourceid>FETCH-LOGICAL-c350t-27ca44778a7f29ee362762f367a2b36b00ad2130bd3099af4ef97db8110e98fc3</originalsourceid><addsrcrecordid>eNpNUMtOwzAQtBCIlsIXICEfuST4lTg5ovIUlbjAOWycDQ1KnBK7Rfl7XNFWnHa0M7OPIeSSs1gJmd0Ixnl8hwa7EoeYq5izIzLlqU6jJM3Y8T88IWfOfTEmEpWxUzIRgudKcDYlHy840hX45Q-MjjZ207cbrAKgq6F3HjxSA9bgQEtwgegt_USL1KGnaIfGLDu0noKFdnSNC6CiHXo4dM7JSQ2tw4tdnZH3h_u3-VO0eH18nt8uIiMT5iOhDSildQa6FjmiTIVORS1TDaKUackYVIJLVlaS5TnUCutcV2XGOcM8q42ckeu_ueHu7zU6X3SNM9i2YLFfu4IzLrRKMpkFqfyTmvCiG7AuVkPTwTAGUbGNtthGW-yjLbgKRHBd7Rasyw6rg2efpfwFJxB3Uw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1012745838</pqid></control><display><type>article</type><title>Key pathways involved in prostate cancer based on gene set enrichment analysis and meta analysis</title><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><creator>Ning, Q Y ; Wu, J Z ; Zang, N ; Liang, J ; Hu, Y L ; Mo, Z N</creator><creatorcontrib>Ning, Q Y ; Wu, J Z ; Zang, N ; Liang, J ; Hu, Y L ; Mo, Z N</creatorcontrib><description>Prostate cancer is one of the most common male malignant neoplasms; however, its causes are not completely understood. A few recent studies have used gene expression profiling of prostate cancer to identify differentially expressed genes and possible relevant pathways. However, few studies have examined the genetic mechanics of prostate cancer at the pathway level to search for such pathways. We used gene set enrichment analysis and a meta-analysis of six independent studies after standardized microarray preprocessing, which increased concordance between these gene datasets. Based on gene set enrichment analysis, there were 12 down- and 25 up-regulated mixing pathways in more than two tissue datasets, while there were two down- and two up-regulated mixing pathways in three cell datasets. Based on the meta-analysis, there were 46 and nine common pathways in the tissue and cell datasets, respectively. Three up- and 10 down-regulated crossing pathways were detected with combined gene set enrichment analysis and meta-analysis. We found that genes with small changes are difficult to detect by classic univariate statistics; they can more easily be identified by pathway analysis. After standardized microarray preprocessing, we applied gene set enrichment analysis and a meta-analysis to increase the concordance in identifying biological mechanisms involved in prostate cancer. The gene pathways that we identified could provide insight concerning the development of prostate cancer.</description><identifier>ISSN: 1676-5680</identifier><identifier>EISSN: 1676-5680</identifier><identifier>DOI: 10.4238/2011.December.14.10</identifier><identifier>PMID: 22194210</identifier><language>eng</language><publisher>Brazil</publisher><subject>Cell Line, Tumor ; Databases, Genetic ; Down-Regulation - genetics ; Gene Expression Profiling ; Gene Expression Regulation, Neoplastic ; Genes, Neoplasm - genetics ; Humans ; Male ; Prostatic Neoplasms - genetics ; RNA, Messenger - genetics ; RNA, Messenger - metabolism ; Signal Transduction - genetics ; Up-Regulation - genetics</subject><ispartof>Genetics and molecular research, 2011-12, Vol.10 (4), p.3856-3887</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c350t-27ca44778a7f29ee362762f367a2b36b00ad2130bd3099af4ef97db8110e98fc3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782,27907,27908</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22194210$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ning, Q Y</creatorcontrib><creatorcontrib>Wu, J Z</creatorcontrib><creatorcontrib>Zang, N</creatorcontrib><creatorcontrib>Liang, J</creatorcontrib><creatorcontrib>Hu, Y L</creatorcontrib><creatorcontrib>Mo, Z N</creatorcontrib><title>Key pathways involved in prostate cancer based on gene set enrichment analysis and meta analysis</title><title>Genetics and molecular research</title><addtitle>Genet Mol Res</addtitle><description>Prostate cancer is one of the most common male malignant neoplasms; however, its causes are not completely understood. A few recent studies have used gene expression profiling of prostate cancer to identify differentially expressed genes and possible relevant pathways. However, few studies have examined the genetic mechanics of prostate cancer at the pathway level to search for such pathways. We used gene set enrichment analysis and a meta-analysis of six independent studies after standardized microarray preprocessing, which increased concordance between these gene datasets. Based on gene set enrichment analysis, there were 12 down- and 25 up-regulated mixing pathways in more than two tissue datasets, while there were two down- and two up-regulated mixing pathways in three cell datasets. Based on the meta-analysis, there were 46 and nine common pathways in the tissue and cell datasets, respectively. Three up- and 10 down-regulated crossing pathways were detected with combined gene set enrichment analysis and meta-analysis. We found that genes with small changes are difficult to detect by classic univariate statistics; they can more easily be identified by pathway analysis. After standardized microarray preprocessing, we applied gene set enrichment analysis and a meta-analysis to increase the concordance in identifying biological mechanisms involved in prostate cancer. The gene pathways that we identified could provide insight concerning the development of prostate cancer.</description><subject>Cell Line, Tumor</subject><subject>Databases, Genetic</subject><subject>Down-Regulation - genetics</subject><subject>Gene Expression Profiling</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Genes, Neoplasm - genetics</subject><subject>Humans</subject><subject>Male</subject><subject>Prostatic Neoplasms - genetics</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Messenger - metabolism</subject><subject>Signal Transduction - genetics</subject><subject>Up-Regulation - genetics</subject><issn>1676-5680</issn><issn>1676-5680</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNUMtOwzAQtBCIlsIXICEfuST4lTg5ovIUlbjAOWycDQ1KnBK7Rfl7XNFWnHa0M7OPIeSSs1gJmd0Ixnl8hwa7EoeYq5izIzLlqU6jJM3Y8T88IWfOfTEmEpWxUzIRgudKcDYlHy840hX45Q-MjjZ207cbrAKgq6F3HjxSA9bgQEtwgegt_USL1KGnaIfGLDu0noKFdnSNC6CiHXo4dM7JSQ2tw4tdnZH3h_u3-VO0eH18nt8uIiMT5iOhDSildQa6FjmiTIVORS1TDaKUackYVIJLVlaS5TnUCutcV2XGOcM8q42ckeu_ueHu7zU6X3SNM9i2YLFfu4IzLrRKMpkFqfyTmvCiG7AuVkPTwTAGUbGNtthGW-yjLbgKRHBd7Rasyw6rg2efpfwFJxB3Uw</recordid><startdate>20111214</startdate><enddate>20111214</enddate><creator>Ning, Q Y</creator><creator>Wu, J Z</creator><creator>Zang, N</creator><creator>Liang, J</creator><creator>Hu, Y L</creator><creator>Mo, Z N</creator><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>7X8</scope></search><sort><creationdate>20111214</creationdate><title>Key pathways involved in prostate cancer based on gene set enrichment analysis and meta analysis</title><author>Ning, Q Y ; Wu, J Z ; Zang, N ; Liang, J ; Hu, Y L ; Mo, Z N</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c350t-27ca44778a7f29ee362762f367a2b36b00ad2130bd3099af4ef97db8110e98fc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Cell Line, Tumor</topic><topic>Databases, Genetic</topic><topic>Down-Regulation - genetics</topic><topic>Gene Expression Profiling</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Genes, Neoplasm - genetics</topic><topic>Humans</topic><topic>Male</topic><topic>Prostatic Neoplasms - genetics</topic><topic>RNA, Messenger - genetics</topic><topic>RNA, Messenger - metabolism</topic><topic>Signal Transduction - genetics</topic><topic>Up-Regulation - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ning, Q Y</creatorcontrib><creatorcontrib>Wu, J Z</creatorcontrib><creatorcontrib>Zang, N</creatorcontrib><creatorcontrib>Liang, J</creatorcontrib><creatorcontrib>Hu, Y L</creatorcontrib><creatorcontrib>Mo, Z N</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Genetics and molecular research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ning, Q Y</au><au>Wu, J Z</au><au>Zang, N</au><au>Liang, J</au><au>Hu, Y L</au><au>Mo, Z N</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Key pathways involved in prostate cancer based on gene set enrichment analysis and meta analysis</atitle><jtitle>Genetics and molecular research</jtitle><addtitle>Genet Mol Res</addtitle><date>2011-12-14</date><risdate>2011</risdate><volume>10</volume><issue>4</issue><spage>3856</spage><epage>3887</epage><pages>3856-3887</pages><issn>1676-5680</issn><eissn>1676-5680</eissn><abstract>Prostate cancer is one of the most common male malignant neoplasms; however, its causes are not completely understood. A few recent studies have used gene expression profiling of prostate cancer to identify differentially expressed genes and possible relevant pathways. However, few studies have examined the genetic mechanics of prostate cancer at the pathway level to search for such pathways. We used gene set enrichment analysis and a meta-analysis of six independent studies after standardized microarray preprocessing, which increased concordance between these gene datasets. Based on gene set enrichment analysis, there were 12 down- and 25 up-regulated mixing pathways in more than two tissue datasets, while there were two down- and two up-regulated mixing pathways in three cell datasets. Based on the meta-analysis, there were 46 and nine common pathways in the tissue and cell datasets, respectively. Three up- and 10 down-regulated crossing pathways were detected with combined gene set enrichment analysis and meta-analysis. We found that genes with small changes are difficult to detect by classic univariate statistics; they can more easily be identified by pathway analysis. After standardized microarray preprocessing, we applied gene set enrichment analysis and a meta-analysis to increase the concordance in identifying biological mechanisms involved in prostate cancer. The gene pathways that we identified could provide insight concerning the development of prostate cancer.</abstract><cop>Brazil</cop><pmid>22194210</pmid><doi>10.4238/2011.December.14.10</doi><tpages>32</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1676-5680
ispartof Genetics and molecular research, 2011-12, Vol.10 (4), p.3856-3887
issn 1676-5680
1676-5680
language eng
recordid cdi_proquest_miscellaneous_1012745838
source MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals
subjects Cell Line, Tumor
Databases, Genetic
Down-Regulation - genetics
Gene Expression Profiling
Gene Expression Regulation, Neoplastic
Genes, Neoplasm - genetics
Humans
Male
Prostatic Neoplasms - genetics
RNA, Messenger - genetics
RNA, Messenger - metabolism
Signal Transduction - genetics
Up-Regulation - genetics
title Key pathways involved in prostate cancer based on gene set enrichment analysis 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=2025-01-16T06%3A56%3A03IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Key%20pathways%20involved%20in%20prostate%20cancer%20based%20on%20gene%20set%20enrichment%20analysis%20and%20meta%20analysis&rft.jtitle=Genetics%20and%20molecular%20research&rft.au=Ning,%20Q%20Y&rft.date=2011-12-14&rft.volume=10&rft.issue=4&rft.spage=3856&rft.epage=3887&rft.pages=3856-3887&rft.issn=1676-5680&rft.eissn=1676-5680&rft_id=info:doi/10.4238/2011.December.14.10&rft_dat=%3Cproquest_cross%3E1012745838%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1012745838&rft_id=info:pmid/22194210&rfr_iscdi=true