Combined analysis of gene expression, miRNA expression and DNA methylation profiles of osteosarcoma
Osteosarcoma (OS) is a common primary malignancy in children and adolescents with relative high survival rate after chemotherapy. While the toxicity of chemotherapy and personalized different response to chemotherapy makes it difficult for the selection of therapeutics and improvement of diagnosis....
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Veröffentlicht in: | Oncology reports 2017-02, Vol.37 (2), p.1175-1181 |
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description | Osteosarcoma (OS) is a common primary malignancy in children and adolescents with relative high survival rate after chemotherapy. While the toxicity of chemotherapy and personalized different response to chemotherapy makes it difficult for the selection of therapeutics and improvement of diagnosis. In this study, we conducted a combined analysis of three types of microarray datasets (gene expression, microRNA (miRNA) expression and DNA methylation) from the Gene Expression Omnibus (GEO). The differential expression genes (DEGs) and miRNAs (DEMI) were screened out via the limma package and differential methylation sites (DMS) were identified by the IMA package. Enriched functions of DEGs and genes contained DMS (DEMs) were obtained through the Database for Annotation, Visualization and Integrated Discovery (DAVID). Besides, miRNA-gene regulation network was obtained based on the pairs of involved DEMIs and overlapping genes between DEMs and DEGs and visualized through Cytoscape software. A total of 583 DEGs and 1051 DMS (corresponding to 827 DEMs) were identified and 56 overlaps were obtained. As expected, most of the expression and methylation profiles of the overlaps exhibited significant negative correlation. The DEGs were mainly enriched in the biological processes related to inflammatory/immune response, cell proliferation, while DEMs were involved in the regulation of gene expression, tissue/organ development. Based on the correlation and network analysis, some novel targets were identified for OS and many known biomarkers were proved in this study, which would be helpful in its early diagnosis and treatment. |
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While the toxicity of chemotherapy and personalized different response to chemotherapy makes it difficult for the selection of therapeutics and improvement of diagnosis. In this study, we conducted a combined analysis of three types of microarray datasets (gene expression, microRNA (miRNA) expression and DNA methylation) from the Gene Expression Omnibus (GEO). The differential expression genes (DEGs) and miRNAs (DEMI) were screened out via the limma package and differential methylation sites (DMS) were identified by the IMA package. Enriched functions of DEGs and genes contained DMS (DEMs) were obtained through the Database for Annotation, Visualization and Integrated Discovery (DAVID). Besides, miRNA-gene regulation network was obtained based on the pairs of involved DEMIs and overlapping genes between DEMs and DEGs and visualized through Cytoscape software. A total of 583 DEGs and 1051 DMS (corresponding to 827 DEMs) were identified and 56 overlaps were obtained. As expected, most of the expression and methylation profiles of the overlaps exhibited significant negative correlation. The DEGs were mainly enriched in the biological processes related to inflammatory/immune response, cell proliferation, while DEMs were involved in the regulation of gene expression, tissue/organ development. Based on the correlation and network analysis, some novel targets were identified for OS and many known biomarkers were proved in this study, which would be helpful in its early diagnosis and treatment.</description><identifier>ISSN: 1021-335X</identifier><identifier>EISSN: 1791-2431</identifier><identifier>DOI: 10.3892/or.2016.5324</identifier><identifier>PMID: 28000890</identifier><language>eng</language><publisher>Greece: D.A. Spandidos</publisher><subject>Analysis ; biomarker ; Biomarkers ; Bone cancer ; Bone Neoplasms - genetics ; Cancer therapies ; Care and treatment ; Chemotherapy ; Cytokines ; Datasets ; Deoxyribonucleic acid ; Diagnosis ; DNA ; DNA Methylation ; Gene expression ; Gene Expression Regulation, Neoplastic ; Gene Regulatory Networks ; Genetic aspects ; GEO ; Health aspects ; Humans ; Kinases ; Medical diagnosis ; Medical prognosis ; Metabolism ; Metastasis ; MicroRNA ; MicroRNAs ; Mutation ; Osteosarcoma ; Osteosarcoma - genetics ; ostesarcoma ; Sarcoma</subject><ispartof>Oncology reports, 2017-02, Vol.37 (2), p.1175-1181</ispartof><rights>Copyright © 2017, Spandidos Publications</rights><rights>COPYRIGHT 2017 Spandidos Publications</rights><rights>Copyright Spandidos Publications UK Ltd. 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c486t-258c15378ef5fd2dd6e1bb2b399c7c68b8e2e6a8bda675846b0a312dd86bbad33</citedby><cites>FETCH-LOGICAL-c486t-258c15378ef5fd2dd6e1bb2b399c7c68b8e2e6a8bda675846b0a312dd86bbad33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28000890$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Wenpeng</creatorcontrib><creatorcontrib>Han, Shiliang</creatorcontrib><creatorcontrib>Sun, Kang</creatorcontrib><title>Combined analysis of gene expression, miRNA expression and DNA methylation profiles of osteosarcoma</title><title>Oncology reports</title><addtitle>Oncol Rep</addtitle><description>Osteosarcoma (OS) is a common primary malignancy in children and adolescents with relative high survival rate after chemotherapy. While the toxicity of chemotherapy and personalized different response to chemotherapy makes it difficult for the selection of therapeutics and improvement of diagnosis. In this study, we conducted a combined analysis of three types of microarray datasets (gene expression, microRNA (miRNA) expression and DNA methylation) from the Gene Expression Omnibus (GEO). The differential expression genes (DEGs) and miRNAs (DEMI) were screened out via the limma package and differential methylation sites (DMS) were identified by the IMA package. Enriched functions of DEGs and genes contained DMS (DEMs) were obtained through the Database for Annotation, Visualization and Integrated Discovery (DAVID). Besides, miRNA-gene regulation network was obtained based on the pairs of involved DEMIs and overlapping genes between DEMs and DEGs and visualized through Cytoscape software. A total of 583 DEGs and 1051 DMS (corresponding to 827 DEMs) were identified and 56 overlaps were obtained. As expected, most of the expression and methylation profiles of the overlaps exhibited significant negative correlation. The DEGs were mainly enriched in the biological processes related to inflammatory/immune response, cell proliferation, while DEMs were involved in the regulation of gene expression, tissue/organ development. Based on the correlation and network analysis, some novel targets were identified for OS and many known biomarkers were proved in this study, which would be helpful in its early diagnosis and treatment.</description><subject>Analysis</subject><subject>biomarker</subject><subject>Biomarkers</subject><subject>Bone cancer</subject><subject>Bone Neoplasms - genetics</subject><subject>Cancer therapies</subject><subject>Care and treatment</subject><subject>Chemotherapy</subject><subject>Cytokines</subject><subject>Datasets</subject><subject>Deoxyribonucleic acid</subject><subject>Diagnosis</subject><subject>DNA</subject><subject>DNA Methylation</subject><subject>Gene expression</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Gene Regulatory Networks</subject><subject>Genetic aspects</subject><subject>GEO</subject><subject>Health aspects</subject><subject>Humans</subject><subject>Kinases</subject><subject>Medical diagnosis</subject><subject>Medical prognosis</subject><subject>Metabolism</subject><subject>Metastasis</subject><subject>MicroRNA</subject><subject>MicroRNAs</subject><subject>Mutation</subject><subject>Osteosarcoma</subject><subject>Osteosarcoma - genetics</subject><subject>ostesarcoma</subject><subject>Sarcoma</subject><issn>1021-335X</issn><issn>1791-2431</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNptkctr3DAQxkVpadK0t56LoZBTvNHDlqXjsn1CaKC00JvQY5xVsK2txgvd_z5yk-YBRYcRH78Z6ZuPkLeMroTS_DzlFadMrlrBm2fkmHWa1bwR7Hm5U85qIdpfR-QV4jWlvKNSvyRHXFFKlabHxG_S6OIEobKTHQ4YsUp9dQUTVPBnlwExpumsGuP3b-tHSqFD9aFII8zbw2DnRdvl1McB_k5IOENCm30a7WvyorcDwpu7ekJ-fvr4Y_Olvrj8_HWzvqh9o-Rc81Z51opOQd_2gYcggTnHndDad14qp4CDtMoFK7tWNdJRK1jhlHTOBiFOyPvbueUjv_eAs7lO-1xsoWG6YVxTJdgDdWUHMHHq05ytHyN6s240Y0JLRgu1-g9VToAx-jTB4vRpw-mjhi3YYd5iGvbLZvApeHYL-pwQM_Rml-No88EwapZETcpmSdQsiRb83Z2pvRsh3MP_Inx4GHcllBgS3jMp16KrKa8Z61pxAz83puc</recordid><startdate>20170201</startdate><enddate>20170201</enddate><creator>Zhang, Wenpeng</creator><creator>Han, Shiliang</creator><creator>Sun, Kang</creator><general>D.A. Spandidos</general><general>Spandidos Publications</general><general>Spandidos Publications UK Ltd</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>3V.</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>AN0</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>20170201</creationdate><title>Combined analysis of gene expression, miRNA expression and DNA methylation profiles of osteosarcoma</title><author>Zhang, Wenpeng ; Han, Shiliang ; Sun, Kang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c486t-258c15378ef5fd2dd6e1bb2b399c7c68b8e2e6a8bda675846b0a312dd86bbad33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Analysis</topic><topic>biomarker</topic><topic>Biomarkers</topic><topic>Bone cancer</topic><topic>Bone Neoplasms - genetics</topic><topic>Cancer therapies</topic><topic>Care and treatment</topic><topic>Chemotherapy</topic><topic>Cytokines</topic><topic>Datasets</topic><topic>Deoxyribonucleic acid</topic><topic>Diagnosis</topic><topic>DNA</topic><topic>DNA Methylation</topic><topic>Gene expression</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Gene Regulatory Networks</topic><topic>Genetic aspects</topic><topic>GEO</topic><topic>Health aspects</topic><topic>Humans</topic><topic>Kinases</topic><topic>Medical diagnosis</topic><topic>Medical prognosis</topic><topic>Metabolism</topic><topic>Metastasis</topic><topic>MicroRNA</topic><topic>MicroRNAs</topic><topic>Mutation</topic><topic>Osteosarcoma</topic><topic>Osteosarcoma - genetics</topic><topic>ostesarcoma</topic><topic>Sarcoma</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Wenpeng</creatorcontrib><creatorcontrib>Han, Shiliang</creatorcontrib><creatorcontrib>Sun, Kang</creatorcontrib><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>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>British Nursing Database</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical 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><jtitle>Oncology reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Wenpeng</au><au>Han, Shiliang</au><au>Sun, Kang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Combined analysis of gene expression, miRNA expression and DNA methylation profiles of osteosarcoma</atitle><jtitle>Oncology reports</jtitle><addtitle>Oncol Rep</addtitle><date>2017-02-01</date><risdate>2017</risdate><volume>37</volume><issue>2</issue><spage>1175</spage><epage>1181</epage><pages>1175-1181</pages><issn>1021-335X</issn><eissn>1791-2431</eissn><abstract>Osteosarcoma (OS) is a common primary malignancy in children and adolescents with relative high survival rate after chemotherapy. While the toxicity of chemotherapy and personalized different response to chemotherapy makes it difficult for the selection of therapeutics and improvement of diagnosis. In this study, we conducted a combined analysis of three types of microarray datasets (gene expression, microRNA (miRNA) expression and DNA methylation) from the Gene Expression Omnibus (GEO). The differential expression genes (DEGs) and miRNAs (DEMI) were screened out via the limma package and differential methylation sites (DMS) were identified by the IMA package. Enriched functions of DEGs and genes contained DMS (DEMs) were obtained through the Database for Annotation, Visualization and Integrated Discovery (DAVID). Besides, miRNA-gene regulation network was obtained based on the pairs of involved DEMIs and overlapping genes between DEMs and DEGs and visualized through Cytoscape software. A total of 583 DEGs and 1051 DMS (corresponding to 827 DEMs) were identified and 56 overlaps were obtained. As expected, most of the expression and methylation profiles of the overlaps exhibited significant negative correlation. The DEGs were mainly enriched in the biological processes related to inflammatory/immune response, cell proliferation, while DEMs were involved in the regulation of gene expression, tissue/organ development. Based on the correlation and network analysis, some novel targets were identified for OS and many known biomarkers were proved in this study, which would be helpful in its early diagnosis and treatment.</abstract><cop>Greece</cop><pub>D.A. Spandidos</pub><pmid>28000890</pmid><doi>10.3892/or.2016.5324</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Analysis biomarker Biomarkers Bone cancer Bone Neoplasms - genetics Cancer therapies Care and treatment Chemotherapy Cytokines Datasets Deoxyribonucleic acid Diagnosis DNA DNA Methylation Gene expression Gene Expression Regulation, Neoplastic Gene Regulatory Networks Genetic aspects GEO Health aspects Humans Kinases Medical diagnosis Medical prognosis Metabolism Metastasis MicroRNA MicroRNAs Mutation Osteosarcoma Osteosarcoma - genetics ostesarcoma Sarcoma |
title | Combined analysis of gene expression, miRNA expression and DNA methylation profiles of osteosarcoma |
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