Global gene expression profiles of human head and neck squamous carcinoma cell lines
For genomewide monitoring and identification of biomarkers of head and neck squamous cell carcinoma (HNSCC), we have conducted a systematic characterization of gene expression profiles, using human cDNA microarrays containing 9K clones, in 25 HNSCC cell lines and 1 immortalized human oral keratinocy...
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creator | Jeon, Geoung A. Lee, Ju‐Seog Patel, Vyomesh Gutkind, J. Silvio Thorgeirsson, Snorri S. Kim, Eun Cheol Chu, In‐Sun Amornphimoltham, Panomwat Park, Myung Hee |
description | For genomewide monitoring and identification of biomarkers of head and neck squamous cell carcinoma (HNSCC), we have conducted a systematic characterization of gene expression profiles, using human cDNA microarrays containing 9K clones, in 25 HNSCC cell lines and 1 immortalized human oral keratinocyte cell line. We used normal human oral keratinocytes (NHOKs) as a reference. Our study showed that genes primarily involved in cell cycle regulation, oncogenesis, cell proliferation, differentiation, apoptosis and cell adhesion were widely altered in the 26 cell lines. Upregulated genes included known oncogenes, protein kinases, DNA‐binding proteins and cell cycle regulators, while those commonly downregulated included differentiation markers, cell adhesion proteins, extracellular matrix proteins, structural proteins (keratins) and protease inhibitor proteins. Compared to NHOK, we observed a striking reduction in the expression of genes involved in terminal differentiation, suggesting that a loss in this process is an important signature of HNSCC. In addition, hierarchical clustering analysis as well as principal component analysis revealed 2 distinctive subtypes of gene expression patterns among the 26 cell lines, reflecting a degree of heterogeneity in HNSCC. By applying significance analysis of microarrays, 128 genes were selected for being distinctively expressed between the 2 groups. Genes differentially expressed in the 2 subgroups include cell proliferation‐related genes, IGFBP6, EGFR and VEGFC; tumor suppression and apoptosis‐related genes such as Tp53, Tp63; as well as cell cycle regulators such as CCND1 and CCND2 (cyclins D1 and D2), suggesting that the 2 subgroups might have undergone different pathways of carcinogenesis. Published 2004 Wiley‐Liss, Inc. |
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Silvio ; Thorgeirsson, Snorri S. ; Kim, Eun Cheol ; Chu, In‐Sun ; Amornphimoltham, Panomwat ; Park, Myung Hee</creator><creatorcontrib>Jeon, Geoung A. ; Lee, Ju‐Seog ; Patel, Vyomesh ; Gutkind, J. Silvio ; Thorgeirsson, Snorri S. ; Kim, Eun Cheol ; Chu, In‐Sun ; Amornphimoltham, Panomwat ; Park, Myung Hee</creatorcontrib><description>For genomewide monitoring and identification of biomarkers of head and neck squamous cell carcinoma (HNSCC), we have conducted a systematic characterization of gene expression profiles, using human cDNA microarrays containing 9K clones, in 25 HNSCC cell lines and 1 immortalized human oral keratinocyte cell line. We used normal human oral keratinocytes (NHOKs) as a reference. Our study showed that genes primarily involved in cell cycle regulation, oncogenesis, cell proliferation, differentiation, apoptosis and cell adhesion were widely altered in the 26 cell lines. Upregulated genes included known oncogenes, protein kinases, DNA‐binding proteins and cell cycle regulators, while those commonly downregulated included differentiation markers, cell adhesion proteins, extracellular matrix proteins, structural proteins (keratins) and protease inhibitor proteins. Compared to NHOK, we observed a striking reduction in the expression of genes involved in terminal differentiation, suggesting that a loss in this process is an important signature of HNSCC. In addition, hierarchical clustering analysis as well as principal component analysis revealed 2 distinctive subtypes of gene expression patterns among the 26 cell lines, reflecting a degree of heterogeneity in HNSCC. By applying significance analysis of microarrays, 128 genes were selected for being distinctively expressed between the 2 groups. Genes differentially expressed in the 2 subgroups include cell proliferation‐related genes, IGFBP6, EGFR and VEGFC; tumor suppression and apoptosis‐related genes such as Tp53, Tp63; as well as cell cycle regulators such as CCND1 and CCND2 (cyclins D1 and D2), suggesting that the 2 subgroups might have undergone different pathways of carcinogenesis. Published 2004 Wiley‐Liss, Inc.</description><identifier>ISSN: 0020-7136</identifier><identifier>EISSN: 1097-0215</identifier><identifier>DOI: 10.1002/ijc.20399</identifier><identifier>PMID: 15352037</identifier><identifier>CODEN: IJCNAW</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Apoptosis ; Biological and medical sciences ; biomarkers ; Biomarkers, Tumor - analysis ; Carcinoma, Squamous Cell - genetics ; Carcinoma, Squamous Cell - pathology ; Cell Adhesion ; Cell Cycle ; Cell Division ; differentiation ; gene expression ; Gene Expression Profiling ; Genes, Tumor Suppressor ; Head and Neck Neoplasms - genetics ; Head and Neck Neoplasms - pathology ; head and neck squamous cell carcinoma ; Humans ; Keratinocytes ; Medical sciences ; microarrays ; Neoplasm Proteins - biosynthesis ; oral cancer ; Otorhinolaryngology (head neck, general aspects and miscellaneous) ; Otorhinolaryngology. Stomatology ; Tumor Cells, Cultured ; tumor progression ; Tumors</subject><ispartof>International journal of cancer, 2004-11, Vol.112 (2), p.249-258</ispartof><rights>Published 2004 Wiley‐Liss, Inc.</rights><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4159-a962e3c97d938fcce8881906b74fce67c30baa8c43836603996f6f559cad9b7e3</citedby><cites>FETCH-LOGICAL-c4159-a962e3c97d938fcce8881906b74fce67c30baa8c43836603996f6f559cad9b7e3</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%2Fijc.20399$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fijc.20399$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16133387$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15352037$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jeon, Geoung A.</creatorcontrib><creatorcontrib>Lee, Ju‐Seog</creatorcontrib><creatorcontrib>Patel, Vyomesh</creatorcontrib><creatorcontrib>Gutkind, J. Silvio</creatorcontrib><creatorcontrib>Thorgeirsson, Snorri S.</creatorcontrib><creatorcontrib>Kim, Eun Cheol</creatorcontrib><creatorcontrib>Chu, In‐Sun</creatorcontrib><creatorcontrib>Amornphimoltham, Panomwat</creatorcontrib><creatorcontrib>Park, Myung Hee</creatorcontrib><title>Global gene expression profiles of human head and neck squamous carcinoma cell lines</title><title>International journal of cancer</title><addtitle>Int J Cancer</addtitle><description>For genomewide monitoring and identification of biomarkers of head and neck squamous cell carcinoma (HNSCC), we have conducted a systematic characterization of gene expression profiles, using human cDNA microarrays containing 9K clones, in 25 HNSCC cell lines and 1 immortalized human oral keratinocyte cell line. We used normal human oral keratinocytes (NHOKs) as a reference. Our study showed that genes primarily involved in cell cycle regulation, oncogenesis, cell proliferation, differentiation, apoptosis and cell adhesion were widely altered in the 26 cell lines. Upregulated genes included known oncogenes, protein kinases, DNA‐binding proteins and cell cycle regulators, while those commonly downregulated included differentiation markers, cell adhesion proteins, extracellular matrix proteins, structural proteins (keratins) and protease inhibitor proteins. Compared to NHOK, we observed a striking reduction in the expression of genes involved in terminal differentiation, suggesting that a loss in this process is an important signature of HNSCC. In addition, hierarchical clustering analysis as well as principal component analysis revealed 2 distinctive subtypes of gene expression patterns among the 26 cell lines, reflecting a degree of heterogeneity in HNSCC. By applying significance analysis of microarrays, 128 genes were selected for being distinctively expressed between the 2 groups. Genes differentially expressed in the 2 subgroups include cell proliferation‐related genes, IGFBP6, EGFR and VEGFC; tumor suppression and apoptosis‐related genes such as Tp53, Tp63; as well as cell cycle regulators such as CCND1 and CCND2 (cyclins D1 and D2), suggesting that the 2 subgroups might have undergone different pathways of carcinogenesis. Published 2004 Wiley‐Liss, Inc.</description><subject>Apoptosis</subject><subject>Biological and medical sciences</subject><subject>biomarkers</subject><subject>Biomarkers, Tumor - analysis</subject><subject>Carcinoma, Squamous Cell - genetics</subject><subject>Carcinoma, Squamous Cell - pathology</subject><subject>Cell Adhesion</subject><subject>Cell Cycle</subject><subject>Cell Division</subject><subject>differentiation</subject><subject>gene expression</subject><subject>Gene Expression Profiling</subject><subject>Genes, Tumor Suppressor</subject><subject>Head and Neck Neoplasms - genetics</subject><subject>Head and Neck Neoplasms - pathology</subject><subject>head and neck squamous cell carcinoma</subject><subject>Humans</subject><subject>Keratinocytes</subject><subject>Medical sciences</subject><subject>microarrays</subject><subject>Neoplasm Proteins - biosynthesis</subject><subject>oral cancer</subject><subject>Otorhinolaryngology (head neck, general aspects and miscellaneous)</subject><subject>Otorhinolaryngology. Stomatology</subject><subject>Tumor Cells, Cultured</subject><subject>tumor progression</subject><subject>Tumors</subject><issn>0020-7136</issn><issn>1097-0215</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kD1PwzAQhi0EglIY-APICwiGFLuOv0ZU8SkkljJHF-cMgcQpMRH03-PSSkww3XDP3b33EHLE2YQzNr2oX91kyoS1W2TEmdUZm3K5TUapxzLNhdoj-zG-Msa5ZPku2eNSyDSgR2R-03QlNPQZA1L8WvQYY90Fuug7XzcYaefpy9BCoC8IFYVQ0YDujcb3AdpuiNRB7-rQtUAdNg1t6oDxgOx4aCIebuqYPF1fzWe32cPjzd3s8iFzOZc2A6umKJzVlRXGO4fGGG6ZKnXuHSrtBCsBjMuFEUqt_lNeeSmtg8qWGsWYnK33prTvA8aPoq3jKgYETNkKbrQ0klslEnr6P6qVUXlyNSbna9D1XYw9-mLR1y30y4KzYmW7SLaLH9uJPd4sHcoWq19yozcBJxsAooPG9xBcHX85xYUQZsVdrLnP5Hz598Xi7n62Pv0NWzyVUw</recordid><startdate>20041101</startdate><enddate>20041101</enddate><creator>Jeon, Geoung A.</creator><creator>Lee, Ju‐Seog</creator><creator>Patel, Vyomesh</creator><creator>Gutkind, J. Silvio</creator><creator>Thorgeirsson, Snorri S.</creator><creator>Kim, Eun Cheol</creator><creator>Chu, In‐Sun</creator><creator>Amornphimoltham, Panomwat</creator><creator>Park, Myung Hee</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><scope>IQODW</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>7TO</scope><scope>H94</scope></search><sort><creationdate>20041101</creationdate><title>Global gene expression profiles of human head and neck squamous carcinoma cell lines</title><author>Jeon, Geoung A. ; Lee, Ju‐Seog ; Patel, Vyomesh ; Gutkind, J. Silvio ; Thorgeirsson, Snorri S. ; Kim, Eun Cheol ; Chu, In‐Sun ; Amornphimoltham, Panomwat ; Park, Myung Hee</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4159-a962e3c97d938fcce8881906b74fce67c30baa8c43836603996f6f559cad9b7e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Apoptosis</topic><topic>Biological and medical sciences</topic><topic>biomarkers</topic><topic>Biomarkers, Tumor - analysis</topic><topic>Carcinoma, Squamous Cell - genetics</topic><topic>Carcinoma, Squamous Cell - pathology</topic><topic>Cell Adhesion</topic><topic>Cell Cycle</topic><topic>Cell Division</topic><topic>differentiation</topic><topic>gene expression</topic><topic>Gene Expression Profiling</topic><topic>Genes, Tumor Suppressor</topic><topic>Head and Neck Neoplasms - genetics</topic><topic>Head and Neck Neoplasms - pathology</topic><topic>head and neck squamous cell carcinoma</topic><topic>Humans</topic><topic>Keratinocytes</topic><topic>Medical sciences</topic><topic>microarrays</topic><topic>Neoplasm Proteins - biosynthesis</topic><topic>oral cancer</topic><topic>Otorhinolaryngology (head neck, general aspects and miscellaneous)</topic><topic>Otorhinolaryngology. Stomatology</topic><topic>Tumor Cells, Cultured</topic><topic>tumor progression</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jeon, Geoung A.</creatorcontrib><creatorcontrib>Lee, Ju‐Seog</creatorcontrib><creatorcontrib>Patel, Vyomesh</creatorcontrib><creatorcontrib>Gutkind, J. 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Silvio</au><au>Thorgeirsson, Snorri S.</au><au>Kim, Eun Cheol</au><au>Chu, In‐Sun</au><au>Amornphimoltham, Panomwat</au><au>Park, Myung Hee</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Global gene expression profiles of human head and neck squamous carcinoma cell lines</atitle><jtitle>International journal of cancer</jtitle><addtitle>Int J Cancer</addtitle><date>2004-11-01</date><risdate>2004</risdate><volume>112</volume><issue>2</issue><spage>249</spage><epage>258</epage><pages>249-258</pages><issn>0020-7136</issn><eissn>1097-0215</eissn><coden>IJCNAW</coden><abstract>For genomewide monitoring and identification of biomarkers of head and neck squamous cell carcinoma (HNSCC), we have conducted a systematic characterization of gene expression profiles, using human cDNA microarrays containing 9K clones, in 25 HNSCC cell lines and 1 immortalized human oral keratinocyte cell line. We used normal human oral keratinocytes (NHOKs) as a reference. Our study showed that genes primarily involved in cell cycle regulation, oncogenesis, cell proliferation, differentiation, apoptosis and cell adhesion were widely altered in the 26 cell lines. Upregulated genes included known oncogenes, protein kinases, DNA‐binding proteins and cell cycle regulators, while those commonly downregulated included differentiation markers, cell adhesion proteins, extracellular matrix proteins, structural proteins (keratins) and protease inhibitor proteins. Compared to NHOK, we observed a striking reduction in the expression of genes involved in terminal differentiation, suggesting that a loss in this process is an important signature of HNSCC. In addition, hierarchical clustering analysis as well as principal component analysis revealed 2 distinctive subtypes of gene expression patterns among the 26 cell lines, reflecting a degree of heterogeneity in HNSCC. By applying significance analysis of microarrays, 128 genes were selected for being distinctively expressed between the 2 groups. Genes differentially expressed in the 2 subgroups include cell proliferation‐related genes, IGFBP6, EGFR and VEGFC; tumor suppression and apoptosis‐related genes such as Tp53, Tp63; as well as cell cycle regulators such as CCND1 and CCND2 (cyclins D1 and D2), suggesting that the 2 subgroups might have undergone different pathways of carcinogenesis. Published 2004 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>15352037</pmid><doi>10.1002/ijc.20399</doi><tpages>10</tpages></addata></record> |
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subjects | Apoptosis Biological and medical sciences biomarkers Biomarkers, Tumor - analysis Carcinoma, Squamous Cell - genetics Carcinoma, Squamous Cell - pathology Cell Adhesion Cell Cycle Cell Division differentiation gene expression Gene Expression Profiling Genes, Tumor Suppressor Head and Neck Neoplasms - genetics Head and Neck Neoplasms - pathology head and neck squamous cell carcinoma Humans Keratinocytes Medical sciences microarrays Neoplasm Proteins - biosynthesis oral cancer Otorhinolaryngology (head neck, general aspects and miscellaneous) Otorhinolaryngology. Stomatology Tumor Cells, Cultured tumor progression Tumors |
title | Global gene expression profiles of human head and neck squamous carcinoma cell lines |
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