Identification of eight candidate target genes of the recurrent 3p12-p14 loss in cervical cancer by integrative genomic profiling
The pathogenetic role, including its target genes, of the recurrent 3p12–p14 loss in cervical cancer has remained unclear. To determine the onset of the event during carcinogenesis, we used microarray techniques and found that the loss was the most frequent 3p event, occurring in 61% of 92 invasive...
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creator | Lando, Malin Wilting, Saskia M Snipstad, Kristin Clancy, Trevor Bierkens, Mariska Aarnes, Eva-Katrine Holden, Marit Stokke, Trond Sundfør, Kolbein Holm, Ruth Kristensen, Gunnar B Steenbergen, Renske DM Lyng, Heidi |
description | The pathogenetic role, including its target genes, of the recurrent 3p12–p14 loss in cervical cancer has remained unclear. To determine the onset of the event during carcinogenesis, we used microarray techniques and found that the loss was the most frequent 3p event, occurring in 61% of 92 invasive carcinomas, in only 2% of 43 high‐grade intraepithelial lesions (CIN2/3), and in 33% of 6 CIN3 lesions adjacent to invasive carcinomas, suggesting a role in acquisition of invasiveness or early during the invasive phase. We performed an integrative DNA copy number and expression analysis of 77 invasive carcinomas, where all genes within the recurrent region were included. We selected eight genes, THOC7, PSMD6, SLC25A26, TMF1, RYBP, SHQ1, EBLN2, and GBE1, which were highly down‐regulated in cases with loss, as confirmed at the protein level for RYBP and TMF1 by immunohistochemistry. The eight genes were subjected to network analysis based on the expression profiles, revealing interaction partners of proteins encoded by the genes that were coordinately regulated in tumours with loss. Several partners were shared among the eight genes, indicating crosstalk in their signalling. Gene ontology analysis showed enrichment of biological processes such as apoptosis, proliferation, and stress response in the network and suggested a relationship between down‐regulation of the eight genes and activation of tumourigenic pathways. Survival analysis showed prognostic impact of the eight‐gene signature that was confirmed in a validation cohort of 74 patients and was independent of clinical parameters. These results support the role of the eight candidate genes as targets of the 3p12–p14 loss in cervical cancer and suggest that the strong selection advantage of the loss during carcinogenesis might be caused by a synergetic effect of several tumourigenic processes controlled by these targets. Copyright © 2013 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd. |
doi_str_mv | 10.1002/path.4168 |
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To determine the onset of the event during carcinogenesis, we used microarray techniques and found that the loss was the most frequent 3p event, occurring in 61% of 92 invasive carcinomas, in only 2% of 43 high‐grade intraepithelial lesions (CIN2/3), and in 33% of 6 CIN3 lesions adjacent to invasive carcinomas, suggesting a role in acquisition of invasiveness or early during the invasive phase. We performed an integrative DNA copy number and expression analysis of 77 invasive carcinomas, where all genes within the recurrent region were included. We selected eight genes, THOC7, PSMD6, SLC25A26, TMF1, RYBP, SHQ1, EBLN2, and GBE1, which were highly down‐regulated in cases with loss, as confirmed at the protein level for RYBP and TMF1 by immunohistochemistry. The eight genes were subjected to network analysis based on the expression profiles, revealing interaction partners of proteins encoded by the genes that were coordinately regulated in tumours with loss. Several partners were shared among the eight genes, indicating crosstalk in their signalling. Gene ontology analysis showed enrichment of biological processes such as apoptosis, proliferation, and stress response in the network and suggested a relationship between down‐regulation of the eight genes and activation of tumourigenic pathways. Survival analysis showed prognostic impact of the eight‐gene signature that was confirmed in a validation cohort of 74 patients and was independent of clinical parameters. These results support the role of the eight candidate genes as targets of the 3p12–p14 loss in cervical cancer and suggest that the strong selection advantage of the loss during carcinogenesis might be caused by a synergetic effect of several tumourigenic processes controlled by these targets. Copyright © 2013 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.</description><identifier>ISSN: 0022-3417</identifier><identifier>EISSN: 1096-9896</identifier><identifier>DOI: 10.1002/path.4168</identifier><identifier>PMID: 23335387</identifier><language>eng</language><publisher>Chichester, UK: John Wiley & Sons, Ltd</publisher><subject>Amino Acid Transport Systems - genetics ; Apoptosis ; Apoptosis - genetics ; array CGH ; Calcium-Binding Proteins - genetics ; carcinogenesis ; Carcinoma, Squamous Cell - genetics ; Carrier Proteins - genetics ; Cervical cancer ; cervical intraepithelial neoplasia ; chromosome 3p ; Chromosomes, Human, Pair 3 - genetics ; DNA-Binding Proteins - genetics ; Female ; gene expression ; Gene Expression Regulation, Neoplastic - genetics ; Genes, Tumor Suppressor ; genetic loss ; Glycogen Debranching Enzyme System - genetics ; Humans ; integrative genomic profiling ; Intracellular Signaling Peptides and Proteins - genetics ; Prognosis ; Proteasome Endopeptidase Complex - genetics ; RNA, Small Interfering - genetics ; RNA-Binding Proteins - genetics ; target genes ; Transcription Factors - genetics ; Transcriptome ; tumour suppressor genes ; Uterine Cervical Neoplasms - genetics</subject><ispartof>The Journal of pathology, 2013-05, Vol.230 (1), p.59-69</ispartof><rights>Copyright © 2013 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4058-62e5e81d572cb6a08e74f5eb3b2a066d855f063e471be8a274c6163e596496143</citedby><cites>FETCH-LOGICAL-c4058-62e5e81d572cb6a08e74f5eb3b2a066d855f063e471be8a274c6163e596496143</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fpath.4168$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fpath.4168$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23335387$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lando, Malin</creatorcontrib><creatorcontrib>Wilting, Saskia M</creatorcontrib><creatorcontrib>Snipstad, Kristin</creatorcontrib><creatorcontrib>Clancy, Trevor</creatorcontrib><creatorcontrib>Bierkens, Mariska</creatorcontrib><creatorcontrib>Aarnes, Eva-Katrine</creatorcontrib><creatorcontrib>Holden, Marit</creatorcontrib><creatorcontrib>Stokke, Trond</creatorcontrib><creatorcontrib>Sundfør, Kolbein</creatorcontrib><creatorcontrib>Holm, Ruth</creatorcontrib><creatorcontrib>Kristensen, Gunnar B</creatorcontrib><creatorcontrib>Steenbergen, Renske DM</creatorcontrib><creatorcontrib>Lyng, Heidi</creatorcontrib><title>Identification of eight candidate target genes of the recurrent 3p12-p14 loss in cervical cancer by integrative genomic profiling</title><title>The Journal of pathology</title><addtitle>J. Pathol</addtitle><description>The pathogenetic role, including its target genes, of the recurrent 3p12–p14 loss in cervical cancer has remained unclear. To determine the onset of the event during carcinogenesis, we used microarray techniques and found that the loss was the most frequent 3p event, occurring in 61% of 92 invasive carcinomas, in only 2% of 43 high‐grade intraepithelial lesions (CIN2/3), and in 33% of 6 CIN3 lesions adjacent to invasive carcinomas, suggesting a role in acquisition of invasiveness or early during the invasive phase. We performed an integrative DNA copy number and expression analysis of 77 invasive carcinomas, where all genes within the recurrent region were included. We selected eight genes, THOC7, PSMD6, SLC25A26, TMF1, RYBP, SHQ1, EBLN2, and GBE1, which were highly down‐regulated in cases with loss, as confirmed at the protein level for RYBP and TMF1 by immunohistochemistry. The eight genes were subjected to network analysis based on the expression profiles, revealing interaction partners of proteins encoded by the genes that were coordinately regulated in tumours with loss. Several partners were shared among the eight genes, indicating crosstalk in their signalling. Gene ontology analysis showed enrichment of biological processes such as apoptosis, proliferation, and stress response in the network and suggested a relationship between down‐regulation of the eight genes and activation of tumourigenic pathways. Survival analysis showed prognostic impact of the eight‐gene signature that was confirmed in a validation cohort of 74 patients and was independent of clinical parameters. These results support the role of the eight candidate genes as targets of the 3p12–p14 loss in cervical cancer and suggest that the strong selection advantage of the loss during carcinogenesis might be caused by a synergetic effect of several tumourigenic processes controlled by these targets. Copyright © 2013 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.</description><subject>Amino Acid Transport Systems - genetics</subject><subject>Apoptosis</subject><subject>Apoptosis - genetics</subject><subject>array CGH</subject><subject>Calcium-Binding Proteins - genetics</subject><subject>carcinogenesis</subject><subject>Carcinoma, Squamous Cell - genetics</subject><subject>Carrier Proteins - genetics</subject><subject>Cervical cancer</subject><subject>cervical intraepithelial neoplasia</subject><subject>chromosome 3p</subject><subject>Chromosomes, Human, Pair 3 - genetics</subject><subject>DNA-Binding Proteins - genetics</subject><subject>Female</subject><subject>gene expression</subject><subject>Gene Expression Regulation, Neoplastic - genetics</subject><subject>Genes, Tumor Suppressor</subject><subject>genetic loss</subject><subject>Glycogen Debranching Enzyme System - genetics</subject><subject>Humans</subject><subject>integrative genomic profiling</subject><subject>Intracellular Signaling Peptides and Proteins - genetics</subject><subject>Prognosis</subject><subject>Proteasome Endopeptidase Complex - genetics</subject><subject>RNA, Small Interfering - genetics</subject><subject>RNA-Binding Proteins - genetics</subject><subject>target genes</subject><subject>Transcription Factors - genetics</subject><subject>Transcriptome</subject><subject>tumour suppressor genes</subject><subject>Uterine Cervical Neoplasms - genetics</subject><issn>0022-3417</issn><issn>1096-9896</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kUtv1DAURi0EokPbBX8AWWIDi7R-xE68bCNoK5WHqlaV2FiOc5NxySTBdgqz5J_jaIYukFj5cc8919aH0GtKTigh7HQycX2SU1k-QytKlMxUqeRztEo1lvGcFgfoVQgPhBClhHiJDhjnXPCyWKHfVw0M0bXOmujGAY8tBtetI7ZmaFxjIuBofAcRdzBAWOpxDdiDnb1PnZhPlGUTzXE_hoDdgC34x2TrF0Pa43qbbiN0Pg14hEUzbpzFkx9b17uhO0IvWtMHON6vh-ju44fb6jK7_nJxVZ1dZzYnoswkAwElbUTBbC0NKaHIWwE1r5khUjalEC2RHPKC1lAaVuRW0nQWSuZK0pwfonc7b5r8Y4YQ9cYFC31vBhjnoBOiGKdKLejbf9CHcfZDep2mnAnGlCjKRL3fUdanr3to9eTdxvitpkQvueglF73kktg3e-Ncb6B5Iv8GkYDTHfDT9bD9v0l_Pbu93CuzXYcLEX49dRj_XcuCF0Lff77QN6yq7qtP3_Q5_wOBAaaA</recordid><startdate>201305</startdate><enddate>201305</enddate><creator>Lando, Malin</creator><creator>Wilting, Saskia M</creator><creator>Snipstad, Kristin</creator><creator>Clancy, Trevor</creator><creator>Bierkens, Mariska</creator><creator>Aarnes, Eva-Katrine</creator><creator>Holden, Marit</creator><creator>Stokke, Trond</creator><creator>Sundfør, Kolbein</creator><creator>Holm, Ruth</creator><creator>Kristensen, Gunnar B</creator><creator>Steenbergen, Renske DM</creator><creator>Lyng, Heidi</creator><general>John Wiley & Sons, Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><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>7QP</scope><scope>7QR</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>201305</creationdate><title>Identification of eight candidate target genes of the recurrent 3p12-p14 loss in cervical cancer by integrative genomic profiling</title><author>Lando, Malin ; Wilting, Saskia M ; Snipstad, Kristin ; Clancy, Trevor ; Bierkens, Mariska ; Aarnes, Eva-Katrine ; Holden, Marit ; Stokke, Trond ; Sundfør, Kolbein ; Holm, Ruth ; Kristensen, Gunnar B ; Steenbergen, Renske DM ; Lyng, Heidi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4058-62e5e81d572cb6a08e74f5eb3b2a066d855f063e471be8a274c6163e596496143</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Amino Acid Transport Systems - genetics</topic><topic>Apoptosis</topic><topic>Apoptosis - genetics</topic><topic>array CGH</topic><topic>Calcium-Binding Proteins - genetics</topic><topic>carcinogenesis</topic><topic>Carcinoma, Squamous Cell - genetics</topic><topic>Carrier Proteins - genetics</topic><topic>Cervical cancer</topic><topic>cervical intraepithelial neoplasia</topic><topic>chromosome 3p</topic><topic>Chromosomes, Human, Pair 3 - genetics</topic><topic>DNA-Binding Proteins - genetics</topic><topic>Female</topic><topic>gene expression</topic><topic>Gene Expression Regulation, Neoplastic - genetics</topic><topic>Genes, Tumor Suppressor</topic><topic>genetic loss</topic><topic>Glycogen Debranching Enzyme System - genetics</topic><topic>Humans</topic><topic>integrative genomic profiling</topic><topic>Intracellular Signaling Peptides and Proteins - genetics</topic><topic>Prognosis</topic><topic>Proteasome Endopeptidase Complex - genetics</topic><topic>RNA, Small Interfering - genetics</topic><topic>RNA-Binding Proteins - genetics</topic><topic>target genes</topic><topic>Transcription Factors - genetics</topic><topic>Transcriptome</topic><topic>tumour suppressor genes</topic><topic>Uterine Cervical Neoplasms - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lando, Malin</creatorcontrib><creatorcontrib>Wilting, Saskia M</creatorcontrib><creatorcontrib>Snipstad, Kristin</creatorcontrib><creatorcontrib>Clancy, Trevor</creatorcontrib><creatorcontrib>Bierkens, Mariska</creatorcontrib><creatorcontrib>Aarnes, Eva-Katrine</creatorcontrib><creatorcontrib>Holden, Marit</creatorcontrib><creatorcontrib>Stokke, Trond</creatorcontrib><creatorcontrib>Sundfør, Kolbein</creatorcontrib><creatorcontrib>Holm, Ruth</creatorcontrib><creatorcontrib>Kristensen, Gunnar B</creatorcontrib><creatorcontrib>Steenbergen, Renske DM</creatorcontrib><creatorcontrib>Lyng, Heidi</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>The Journal of pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lando, Malin</au><au>Wilting, Saskia M</au><au>Snipstad, Kristin</au><au>Clancy, Trevor</au><au>Bierkens, Mariska</au><au>Aarnes, Eva-Katrine</au><au>Holden, Marit</au><au>Stokke, Trond</au><au>Sundfør, Kolbein</au><au>Holm, Ruth</au><au>Kristensen, Gunnar B</au><au>Steenbergen, Renske DM</au><au>Lyng, Heidi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification of eight candidate target genes of the recurrent 3p12-p14 loss in cervical cancer by integrative genomic profiling</atitle><jtitle>The Journal of pathology</jtitle><addtitle>J. Pathol</addtitle><date>2013-05</date><risdate>2013</risdate><volume>230</volume><issue>1</issue><spage>59</spage><epage>69</epage><pages>59-69</pages><issn>0022-3417</issn><eissn>1096-9896</eissn><abstract>The pathogenetic role, including its target genes, of the recurrent 3p12–p14 loss in cervical cancer has remained unclear. To determine the onset of the event during carcinogenesis, we used microarray techniques and found that the loss was the most frequent 3p event, occurring in 61% of 92 invasive carcinomas, in only 2% of 43 high‐grade intraepithelial lesions (CIN2/3), and in 33% of 6 CIN3 lesions adjacent to invasive carcinomas, suggesting a role in acquisition of invasiveness or early during the invasive phase. We performed an integrative DNA copy number and expression analysis of 77 invasive carcinomas, where all genes within the recurrent region were included. We selected eight genes, THOC7, PSMD6, SLC25A26, TMF1, RYBP, SHQ1, EBLN2, and GBE1, which were highly down‐regulated in cases with loss, as confirmed at the protein level for RYBP and TMF1 by immunohistochemistry. The eight genes were subjected to network analysis based on the expression profiles, revealing interaction partners of proteins encoded by the genes that were coordinately regulated in tumours with loss. Several partners were shared among the eight genes, indicating crosstalk in their signalling. Gene ontology analysis showed enrichment of biological processes such as apoptosis, proliferation, and stress response in the network and suggested a relationship between down‐regulation of the eight genes and activation of tumourigenic pathways. Survival analysis showed prognostic impact of the eight‐gene signature that was confirmed in a validation cohort of 74 patients and was independent of clinical parameters. These results support the role of the eight candidate genes as targets of the 3p12–p14 loss in cervical cancer and suggest that the strong selection advantage of the loss during carcinogenesis might be caused by a synergetic effect of several tumourigenic processes controlled by these targets. Copyright © 2013 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.</abstract><cop>Chichester, UK</cop><pub>John Wiley & Sons, Ltd</pub><pmid>23335387</pmid><doi>10.1002/path.4168</doi><tpages>11</tpages></addata></record> |
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subjects | Amino Acid Transport Systems - genetics Apoptosis Apoptosis - genetics array CGH Calcium-Binding Proteins - genetics carcinogenesis Carcinoma, Squamous Cell - genetics Carrier Proteins - genetics Cervical cancer cervical intraepithelial neoplasia chromosome 3p Chromosomes, Human, Pair 3 - genetics DNA-Binding Proteins - genetics Female gene expression Gene Expression Regulation, Neoplastic - genetics Genes, Tumor Suppressor genetic loss Glycogen Debranching Enzyme System - genetics Humans integrative genomic profiling Intracellular Signaling Peptides and Proteins - genetics Prognosis Proteasome Endopeptidase Complex - genetics RNA, Small Interfering - genetics RNA-Binding Proteins - genetics target genes Transcription Factors - genetics Transcriptome tumour suppressor genes Uterine Cervical Neoplasms - genetics |
title | Identification of eight candidate target genes of the recurrent 3p12-p14 loss in cervical cancer by integrative genomic profiling |
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