MicroRNA Classifiers for Predicting Prognosis of Squamous Cell Lung Cancer

Non-small cell lung cancer (NSCLC), which is comprised mainly of adenocarcinoma and squamous cell carcinoma (SCC), is the cause of 80% of all lung cancer deaths in the United States. NSCLC is also associated with a high rate of relapse after clinical treatment and, therefore, requires robust prognos...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Cancer research (Chicago, Ill.) Ill.), 2009-07, Vol.69 (14), p.5776-5783
Hauptverfasser: RAPONI, Mitch, DOSSEY, Lesley, JATKOE, Tim, XIAOYING WU, GUOAN CHEN, HONGTAO FAN, BEER, David G
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 5783
container_issue 14
container_start_page 5776
container_title Cancer research (Chicago, Ill.)
container_volume 69
creator RAPONI, Mitch
DOSSEY, Lesley
JATKOE, Tim
XIAOYING WU
GUOAN CHEN
HONGTAO FAN
BEER, David G
description Non-small cell lung cancer (NSCLC), which is comprised mainly of adenocarcinoma and squamous cell carcinoma (SCC), is the cause of 80% of all lung cancer deaths in the United States. NSCLC is also associated with a high rate of relapse after clinical treatment and, therefore, requires robust prognostic markers to better manage therapy options. The aim of this study was to identify microRNA (miRNA) expression profiles in SCC of the lung that would better predict prognosis. Total RNA from 61 SCC samples and 10 matched normal lung samples was processed for small RNA species and profiled on MirVana miRNA Bioarrays (version 2, Ambion). We identified 15 miRNAs that were differentially expressed between normal lung and SCC, including members of the miR-17-92 cluster and its paralogues. We also identified miRNAs, including miR-155 and let-7, which had previously been shown to have prognostic value in adenocarcinoma. Based on cross-fold validation analyses, miR-146b alone was found to have the strongest prediction accuracy for stratifying prognostic groups at approximately 78%. The miRNA signatures were superior in predicting overall survival than a previously described 50-gene prognostic signature. Whereas there was no overlap between the mRNAs targeted by the prognostic miRNAs and the 50-gene expression signature, there was a significant overlap in the corresponding biological pathways, including fibroblast growth factor and interleukin-6 signaling. Our data indicate that miRNAs may have greater clinical utility in predicting the prognosis of patients with squamous cell lung carcinomas than mRNA-based signatures.
doi_str_mv 10.1158/0008-5472.can-09-0587
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_67495182</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>67495182</sourcerecordid><originalsourceid>FETCH-LOGICAL-c536t-3c1f0087aed1fb3400cdb72e11599931a7455f30e69e70ad851ec6e2f5c3d2643</originalsourceid><addsrcrecordid>eNpFkFtPwyAYhonRuDn9CZre6F0VCl-By6XxmDmNh2vCKCyYrt1gvfDfS7NlXgHh-eB9H4QuCb4lBMQdxljkwHhxa3SbY5ljEPwIjQlQkXPG4BiND8wIncX4k45AMJyiEZEgWMHpGL28ehO6j_k0qxodo3fehpi5LmTvwdbebH27TNtu2XbRx6xz2eem16uuj1llmyab9em-0q2x4RydON1Ee7FfJ-j74f6respnb4_P1XSWG6DlNqeGuJSLa1sTt6AMY1MveGFTKyklJZozAEexLaXlWNcCiDWlLRwYWhcloxN0s3t3HbpNb-NWrXw0KYxubcqlSs4kEFEkEHZgahhjsE6tg1_p8KsIVoNENQhSgyBVTecKSzVITHNX-w_6xcrW_1N7awm43gM6Gt24kPr7eOAKIgQDIekfCRh5sA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>67495182</pqid></control><display><type>article</type><title>MicroRNA Classifiers for Predicting Prognosis of Squamous Cell Lung Cancer</title><source>MEDLINE</source><source>American Association for Cancer Research</source><source>EZB-FREE-00999 freely available EZB journals</source><creator>RAPONI, Mitch ; DOSSEY, Lesley ; JATKOE, Tim ; XIAOYING WU ; GUOAN CHEN ; HONGTAO FAN ; BEER, David G</creator><creatorcontrib>RAPONI, Mitch ; DOSSEY, Lesley ; JATKOE, Tim ; XIAOYING WU ; GUOAN CHEN ; HONGTAO FAN ; BEER, David G</creatorcontrib><description>Non-small cell lung cancer (NSCLC), which is comprised mainly of adenocarcinoma and squamous cell carcinoma (SCC), is the cause of 80% of all lung cancer deaths in the United States. NSCLC is also associated with a high rate of relapse after clinical treatment and, therefore, requires robust prognostic markers to better manage therapy options. The aim of this study was to identify microRNA (miRNA) expression profiles in SCC of the lung that would better predict prognosis. Total RNA from 61 SCC samples and 10 matched normal lung samples was processed for small RNA species and profiled on MirVana miRNA Bioarrays (version 2, Ambion). We identified 15 miRNAs that were differentially expressed between normal lung and SCC, including members of the miR-17-92 cluster and its paralogues. We also identified miRNAs, including miR-155 and let-7, which had previously been shown to have prognostic value in adenocarcinoma. Based on cross-fold validation analyses, miR-146b alone was found to have the strongest prediction accuracy for stratifying prognostic groups at approximately 78%. The miRNA signatures were superior in predicting overall survival than a previously described 50-gene prognostic signature. Whereas there was no overlap between the mRNAs targeted by the prognostic miRNAs and the 50-gene expression signature, there was a significant overlap in the corresponding biological pathways, including fibroblast growth factor and interleukin-6 signaling. Our data indicate that miRNAs may have greater clinical utility in predicting the prognosis of patients with squamous cell lung carcinomas than mRNA-based signatures.</description><identifier>ISSN: 0008-5472</identifier><identifier>EISSN: 1538-7445</identifier><identifier>DOI: 10.1158/0008-5472.can-09-0587</identifier><identifier>PMID: 19584273</identifier><identifier>CODEN: CNREA8</identifier><language>eng</language><publisher>Philadelphia, PA: American Association for Cancer Research</publisher><subject>Aged ; Aged, 80 and over ; Antineoplastic agents ; Biological and medical sciences ; Carcinoma, Squamous Cell - classification ; Carcinoma, Squamous Cell - genetics ; Carcinoma, Squamous Cell - pathology ; Female ; Follow-Up Studies ; Gene Expression Profiling ; Gene Expression Regulation, Neoplastic ; Humans ; Lung Neoplasms - classification ; Lung Neoplasms - genetics ; Lung Neoplasms - pathology ; Male ; Medical sciences ; MicroRNAs - genetics ; Middle Aged ; Oligonucleotide Array Sequence Analysis ; Pharmacology. Drug treatments ; Prognosis ; Reverse Transcriptase Polymerase Chain Reaction ; Survival Analysis ; Tumors</subject><ispartof>Cancer research (Chicago, Ill.), 2009-07, Vol.69 (14), p.5776-5783</ispartof><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c536t-3c1f0087aed1fb3400cdb72e11599931a7455f30e69e70ad851ec6e2f5c3d2643</citedby><cites>FETCH-LOGICAL-c536t-3c1f0087aed1fb3400cdb72e11599931a7455f30e69e70ad851ec6e2f5c3d2643</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,3343,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=21884589$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19584273$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>RAPONI, Mitch</creatorcontrib><creatorcontrib>DOSSEY, Lesley</creatorcontrib><creatorcontrib>JATKOE, Tim</creatorcontrib><creatorcontrib>XIAOYING WU</creatorcontrib><creatorcontrib>GUOAN CHEN</creatorcontrib><creatorcontrib>HONGTAO FAN</creatorcontrib><creatorcontrib>BEER, David G</creatorcontrib><title>MicroRNA Classifiers for Predicting Prognosis of Squamous Cell Lung Cancer</title><title>Cancer research (Chicago, Ill.)</title><addtitle>Cancer Res</addtitle><description>Non-small cell lung cancer (NSCLC), which is comprised mainly of adenocarcinoma and squamous cell carcinoma (SCC), is the cause of 80% of all lung cancer deaths in the United States. NSCLC is also associated with a high rate of relapse after clinical treatment and, therefore, requires robust prognostic markers to better manage therapy options. The aim of this study was to identify microRNA (miRNA) expression profiles in SCC of the lung that would better predict prognosis. Total RNA from 61 SCC samples and 10 matched normal lung samples was processed for small RNA species and profiled on MirVana miRNA Bioarrays (version 2, Ambion). We identified 15 miRNAs that were differentially expressed between normal lung and SCC, including members of the miR-17-92 cluster and its paralogues. We also identified miRNAs, including miR-155 and let-7, which had previously been shown to have prognostic value in adenocarcinoma. Based on cross-fold validation analyses, miR-146b alone was found to have the strongest prediction accuracy for stratifying prognostic groups at approximately 78%. The miRNA signatures were superior in predicting overall survival than a previously described 50-gene prognostic signature. Whereas there was no overlap between the mRNAs targeted by the prognostic miRNAs and the 50-gene expression signature, there was a significant overlap in the corresponding biological pathways, including fibroblast growth factor and interleukin-6 signaling. Our data indicate that miRNAs may have greater clinical utility in predicting the prognosis of patients with squamous cell lung carcinomas than mRNA-based signatures.</description><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Antineoplastic agents</subject><subject>Biological and medical sciences</subject><subject>Carcinoma, Squamous Cell - classification</subject><subject>Carcinoma, Squamous Cell - genetics</subject><subject>Carcinoma, Squamous Cell - pathology</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Gene Expression Profiling</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Humans</subject><subject>Lung Neoplasms - classification</subject><subject>Lung Neoplasms - genetics</subject><subject>Lung Neoplasms - pathology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>MicroRNAs - genetics</subject><subject>Middle Aged</subject><subject>Oligonucleotide Array Sequence Analysis</subject><subject>Pharmacology. Drug treatments</subject><subject>Prognosis</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>Survival Analysis</subject><subject>Tumors</subject><issn>0008-5472</issn><issn>1538-7445</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkFtPwyAYhonRuDn9CZre6F0VCl-By6XxmDmNh2vCKCyYrt1gvfDfS7NlXgHh-eB9H4QuCb4lBMQdxljkwHhxa3SbY5ljEPwIjQlQkXPG4BiND8wIncX4k45AMJyiEZEgWMHpGL28ehO6j_k0qxodo3fehpi5LmTvwdbebH27TNtu2XbRx6xz2eem16uuj1llmyab9em-0q2x4RydON1Ee7FfJ-j74f6respnb4_P1XSWG6DlNqeGuJSLa1sTt6AMY1MveGFTKyklJZozAEexLaXlWNcCiDWlLRwYWhcloxN0s3t3HbpNb-NWrXw0KYxubcqlSs4kEFEkEHZgahhjsE6tg1_p8KsIVoNENQhSgyBVTecKSzVITHNX-w_6xcrW_1N7awm43gM6Gt24kPr7eOAKIgQDIekfCRh5sA</recordid><startdate>20090715</startdate><enddate>20090715</enddate><creator>RAPONI, Mitch</creator><creator>DOSSEY, Lesley</creator><creator>JATKOE, Tim</creator><creator>XIAOYING WU</creator><creator>GUOAN CHEN</creator><creator>HONGTAO FAN</creator><creator>BEER, David G</creator><general>American Association for Cancer Research</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>7X8</scope></search><sort><creationdate>20090715</creationdate><title>MicroRNA Classifiers for Predicting Prognosis of Squamous Cell Lung Cancer</title><author>RAPONI, Mitch ; DOSSEY, Lesley ; JATKOE, Tim ; XIAOYING WU ; GUOAN CHEN ; HONGTAO FAN ; BEER, David G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c536t-3c1f0087aed1fb3400cdb72e11599931a7455f30e69e70ad851ec6e2f5c3d2643</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Antineoplastic agents</topic><topic>Biological and medical sciences</topic><topic>Carcinoma, Squamous Cell - classification</topic><topic>Carcinoma, Squamous Cell - genetics</topic><topic>Carcinoma, Squamous Cell - pathology</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Gene Expression Profiling</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Humans</topic><topic>Lung Neoplasms - classification</topic><topic>Lung Neoplasms - genetics</topic><topic>Lung Neoplasms - pathology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>MicroRNAs - genetics</topic><topic>Middle Aged</topic><topic>Oligonucleotide Array Sequence Analysis</topic><topic>Pharmacology. Drug treatments</topic><topic>Prognosis</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>Survival Analysis</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>RAPONI, Mitch</creatorcontrib><creatorcontrib>DOSSEY, Lesley</creatorcontrib><creatorcontrib>JATKOE, Tim</creatorcontrib><creatorcontrib>XIAOYING WU</creatorcontrib><creatorcontrib>GUOAN CHEN</creatorcontrib><creatorcontrib>HONGTAO FAN</creatorcontrib><creatorcontrib>BEER, David G</creatorcontrib><collection>Pascal-Francis</collection><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>Cancer research (Chicago, Ill.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>RAPONI, Mitch</au><au>DOSSEY, Lesley</au><au>JATKOE, Tim</au><au>XIAOYING WU</au><au>GUOAN CHEN</au><au>HONGTAO FAN</au><au>BEER, David G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>MicroRNA Classifiers for Predicting Prognosis of Squamous Cell Lung Cancer</atitle><jtitle>Cancer research (Chicago, Ill.)</jtitle><addtitle>Cancer Res</addtitle><date>2009-07-15</date><risdate>2009</risdate><volume>69</volume><issue>14</issue><spage>5776</spage><epage>5783</epage><pages>5776-5783</pages><issn>0008-5472</issn><eissn>1538-7445</eissn><coden>CNREA8</coden><abstract>Non-small cell lung cancer (NSCLC), which is comprised mainly of adenocarcinoma and squamous cell carcinoma (SCC), is the cause of 80% of all lung cancer deaths in the United States. NSCLC is also associated with a high rate of relapse after clinical treatment and, therefore, requires robust prognostic markers to better manage therapy options. The aim of this study was to identify microRNA (miRNA) expression profiles in SCC of the lung that would better predict prognosis. Total RNA from 61 SCC samples and 10 matched normal lung samples was processed for small RNA species and profiled on MirVana miRNA Bioarrays (version 2, Ambion). We identified 15 miRNAs that were differentially expressed between normal lung and SCC, including members of the miR-17-92 cluster and its paralogues. We also identified miRNAs, including miR-155 and let-7, which had previously been shown to have prognostic value in adenocarcinoma. Based on cross-fold validation analyses, miR-146b alone was found to have the strongest prediction accuracy for stratifying prognostic groups at approximately 78%. The miRNA signatures were superior in predicting overall survival than a previously described 50-gene prognostic signature. Whereas there was no overlap between the mRNAs targeted by the prognostic miRNAs and the 50-gene expression signature, there was a significant overlap in the corresponding biological pathways, including fibroblast growth factor and interleukin-6 signaling. Our data indicate that miRNAs may have greater clinical utility in predicting the prognosis of patients with squamous cell lung carcinomas than mRNA-based signatures.</abstract><cop>Philadelphia, PA</cop><pub>American Association for Cancer Research</pub><pmid>19584273</pmid><doi>10.1158/0008-5472.can-09-0587</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0008-5472
ispartof Cancer research (Chicago, Ill.), 2009-07, Vol.69 (14), p.5776-5783
issn 0008-5472
1538-7445
language eng
recordid cdi_proquest_miscellaneous_67495182
source MEDLINE; American Association for Cancer Research; EZB-FREE-00999 freely available EZB journals
subjects Aged
Aged, 80 and over
Antineoplastic agents
Biological and medical sciences
Carcinoma, Squamous Cell - classification
Carcinoma, Squamous Cell - genetics
Carcinoma, Squamous Cell - pathology
Female
Follow-Up Studies
Gene Expression Profiling
Gene Expression Regulation, Neoplastic
Humans
Lung Neoplasms - classification
Lung Neoplasms - genetics
Lung Neoplasms - pathology
Male
Medical sciences
MicroRNAs - genetics
Middle Aged
Oligonucleotide Array Sequence Analysis
Pharmacology. Drug treatments
Prognosis
Reverse Transcriptase Polymerase Chain Reaction
Survival Analysis
Tumors
title MicroRNA Classifiers for Predicting Prognosis of Squamous Cell Lung Cancer
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-01T00%3A22%3A15IST&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=MicroRNA%20Classifiers%20for%20Predicting%20Prognosis%20of%20Squamous%20Cell%20Lung%20Cancer&rft.jtitle=Cancer%20research%20(Chicago,%20Ill.)&rft.au=RAPONI,%20Mitch&rft.date=2009-07-15&rft.volume=69&rft.issue=14&rft.spage=5776&rft.epage=5783&rft.pages=5776-5783&rft.issn=0008-5472&rft.eissn=1538-7445&rft.coden=CNREA8&rft_id=info:doi/10.1158/0008-5472.can-09-0587&rft_dat=%3Cproquest_cross%3E67495182%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=67495182&rft_id=info:pmid/19584273&rfr_iscdi=true