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MiRNA-196 Is Upregulated in Glioblastoma But Not in Anaplastic Astrocytoma and Has Prognostic Significance
MicroRNAs (miRNA) are short noncoding RNAs that can play critical roles in diverse biological processes. They are implicated in tumorigenesis and function both as tumor suppressors and as oncogenes. The clinical significance of miRNA expression profiles in malignant gliomas remains unclear. In this...
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Published in: | Clinical cancer research 2010-08, Vol.16 (16), p.4289-4297 |
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creator | YANLEI GUAN MIZOGUCHI, Masahiro XINLONG MA HAYASHI, Kenshi SASAKI, Tomio YOSHIMOTO, Koji HATA, Nobuhiro SHONO, Tadahisa SUZUKI, Satoshi O ARAKI, Yukie KUGA, Daisuke NAKAMIZO, Akira AMANO, Toshiyuki |
description | MicroRNAs (miRNA) are short noncoding RNAs that can play critical roles in diverse biological processes. They are implicated in tumorigenesis and function both as tumor suppressors and as oncogenes. The clinical significance of miRNA expression profiles in malignant gliomas remains unclear.
In this study, we examined the expression levels of 365 mature human miRNAs in 12 malignant gliomas, including 8 glioblastomas and 4 anaplastic astrocytomas, using TaqMan real-time quantitative PCR arrays. A validation study was done to corroborate a subset of the results, including expression levels of miR-196a, -196b, -21, and -15b, by analyzing 92 malignant gliomas by conventional real-time PCR. We modeled the relationship between the expression levels of these miRNAs and the survival rate of 39 glioblastoma patients by Kaplan-Meier method and multivariate analysis.
Expression profiles in glioblastomas and anaplastic astrocytomas suggested that 16 miRNAs were candidate markers associated with the malignant progression of gliomas. Among them, miR-196a showed the most significant difference (P = 0.0038), with miR-196b also having a high significance (P = 0.0371). Both miRNAs showed increased expression levels in glioblastomas relative to both anaplastic astrocytomas and normal brains in the validation study. Furthermore, patients with high miR-196 expression levels showed significantly poorer survival by the Kaplan-Meier method (P = 0.0073). Multivariate analysis showed that miR-196 expression levels were an independent predictor of overall survival in all 39 glioblastoma patients (P = 0.021; hazard ratio, 2.81).
Our results suggest that miR-196 may play a role in the malignant progression of gliomas and may be a prognostic predictor in glioblastomas. |
doi_str_mv | 10.1158/1078-0432.CCR-10-0207 |
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In this study, we examined the expression levels of 365 mature human miRNAs in 12 malignant gliomas, including 8 glioblastomas and 4 anaplastic astrocytomas, using TaqMan real-time quantitative PCR arrays. A validation study was done to corroborate a subset of the results, including expression levels of miR-196a, -196b, -21, and -15b, by analyzing 92 malignant gliomas by conventional real-time PCR. We modeled the relationship between the expression levels of these miRNAs and the survival rate of 39 glioblastoma patients by Kaplan-Meier method and multivariate analysis.
Expression profiles in glioblastomas and anaplastic astrocytomas suggested that 16 miRNAs were candidate markers associated with the malignant progression of gliomas. Among them, miR-196a showed the most significant difference (P = 0.0038), with miR-196b also having a high significance (P = 0.0371). Both miRNAs showed increased expression levels in glioblastomas relative to both anaplastic astrocytomas and normal brains in the validation study. Furthermore, patients with high miR-196 expression levels showed significantly poorer survival by the Kaplan-Meier method (P = 0.0073). Multivariate analysis showed that miR-196 expression levels were an independent predictor of overall survival in all 39 glioblastoma patients (P = 0.021; hazard ratio, 2.81).
Our results suggest that miR-196 may play a role in the malignant progression of gliomas and may be a prognostic predictor in glioblastomas.</description><identifier>ISSN: 1078-0432</identifier><identifier>EISSN: 1557-3265</identifier><identifier>DOI: 10.1158/1078-0432.CCR-10-0207</identifier><identifier>PMID: 20601442</identifier><identifier>CODEN: CCREF4</identifier><language>eng</language><publisher>Philadelphia, PA: American Association for Cancer Research</publisher><subject>Antineoplastic agents ; Astrocytoma - genetics ; Astrocytoma - mortality ; Astrocytoma - pathology ; Biological and medical sciences ; Biomarkers, Tumor - genetics ; Brain Neoplasms - genetics ; Brain Neoplasms - mortality ; Brain Neoplasms - pathology ; Gene Expression ; Gene Expression Profiling ; Glioblastoma - genetics ; Glioblastoma - mortality ; Glioblastoma - pathology ; Humans ; Kaplan-Meier Estimate ; Loss of Heterozygosity ; Medical sciences ; MicroRNAs - genetics ; Microsatellite Repeats ; Neurology ; Pharmacology. Drug treatments ; Prognosis ; Reverse Transcriptase Polymerase Chain Reaction ; Tumors of the nervous system. Phacomatoses ; Up-Regulation</subject><ispartof>Clinical cancer research, 2010-08, Vol.16 (16), p.4289-4297</ispartof><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c469t-463b0cb285be35ce313a464f08756e4ec70d6f2a7f7447efaba2e392db4c8aae3</citedby><cites>FETCH-LOGICAL-c469t-463b0cb285be35ce313a464f08756e4ec70d6f2a7f7447efaba2e392db4c8aae3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23154425$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20601442$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>YANLEI GUAN</creatorcontrib><creatorcontrib>MIZOGUCHI, Masahiro</creatorcontrib><creatorcontrib>XINLONG MA</creatorcontrib><creatorcontrib>HAYASHI, Kenshi</creatorcontrib><creatorcontrib>SASAKI, Tomio</creatorcontrib><creatorcontrib>YOSHIMOTO, Koji</creatorcontrib><creatorcontrib>HATA, Nobuhiro</creatorcontrib><creatorcontrib>SHONO, Tadahisa</creatorcontrib><creatorcontrib>SUZUKI, Satoshi O</creatorcontrib><creatorcontrib>ARAKI, Yukie</creatorcontrib><creatorcontrib>KUGA, Daisuke</creatorcontrib><creatorcontrib>NAKAMIZO, Akira</creatorcontrib><creatorcontrib>AMANO, Toshiyuki</creatorcontrib><title>MiRNA-196 Is Upregulated in Glioblastoma But Not in Anaplastic Astrocytoma and Has Prognostic Significance</title><title>Clinical cancer research</title><addtitle>Clin Cancer Res</addtitle><description>MicroRNAs (miRNA) are short noncoding RNAs that can play critical roles in diverse biological processes. They are implicated in tumorigenesis and function both as tumor suppressors and as oncogenes. The clinical significance of miRNA expression profiles in malignant gliomas remains unclear.
In this study, we examined the expression levels of 365 mature human miRNAs in 12 malignant gliomas, including 8 glioblastomas and 4 anaplastic astrocytomas, using TaqMan real-time quantitative PCR arrays. A validation study was done to corroborate a subset of the results, including expression levels of miR-196a, -196b, -21, and -15b, by analyzing 92 malignant gliomas by conventional real-time PCR. We modeled the relationship between the expression levels of these miRNAs and the survival rate of 39 glioblastoma patients by Kaplan-Meier method and multivariate analysis.
Expression profiles in glioblastomas and anaplastic astrocytomas suggested that 16 miRNAs were candidate markers associated with the malignant progression of gliomas. Among them, miR-196a showed the most significant difference (P = 0.0038), with miR-196b also having a high significance (P = 0.0371). Both miRNAs showed increased expression levels in glioblastomas relative to both anaplastic astrocytomas and normal brains in the validation study. Furthermore, patients with high miR-196 expression levels showed significantly poorer survival by the Kaplan-Meier method (P = 0.0073). Multivariate analysis showed that miR-196 expression levels were an independent predictor of overall survival in all 39 glioblastoma patients (P = 0.021; hazard ratio, 2.81).
Our results suggest that miR-196 may play a role in the malignant progression of gliomas and may be a prognostic predictor in glioblastomas.</description><subject>Antineoplastic agents</subject><subject>Astrocytoma - genetics</subject><subject>Astrocytoma - mortality</subject><subject>Astrocytoma - pathology</subject><subject>Biological and medical sciences</subject><subject>Biomarkers, Tumor - genetics</subject><subject>Brain Neoplasms - genetics</subject><subject>Brain Neoplasms - mortality</subject><subject>Brain Neoplasms - pathology</subject><subject>Gene Expression</subject><subject>Gene Expression Profiling</subject><subject>Glioblastoma - genetics</subject><subject>Glioblastoma - mortality</subject><subject>Glioblastoma - pathology</subject><subject>Humans</subject><subject>Kaplan-Meier Estimate</subject><subject>Loss of Heterozygosity</subject><subject>Medical sciences</subject><subject>MicroRNAs - genetics</subject><subject>Microsatellite Repeats</subject><subject>Neurology</subject><subject>Pharmacology. Drug treatments</subject><subject>Prognosis</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>Tumors of the nervous system. Phacomatoses</subject><subject>Up-Regulation</subject><issn>1078-0432</issn><issn>1557-3265</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNqFkctOwzAQRS0EolD4BJA3iFWKn7GzLBWPSrxUYB1NHKcySuNiJ4v-PQm0sGQ1oztnZqR7ETqjZEKp1FeUKJ0QwdlkNlsklCSEEbWHjqiUKuEslft9v2NG6DjGD0KooEQcohEjad8LdoQ-Ht3iaZrQLMXziN_XwS67GlpbYtfgu9r5oobY-hXg667FT74d9GkD60F2Bk9jG7zZfBPQlPgeIn4Jftn47_GrWzaucgYaY0_QQQV1tKfbOkbvtzdvs_vk4fluPps-JEakWZuIlBfEFEzLwnJpLKccRCoqopVMrbBGkTKtGKhKCaFsBQUwyzNWFsJoAMvH6PLn7jr4z87GNl-5aGxdQ2N9F3OtlMxYJvS_pBI6k4xq2pPyhzTBxxhsla-DW0HY5JTkQx754HU-eJ33eQzqkEe_d7790BUrW_5u7QLogYstANFAXYXeKRf_OE5lj0n-BSNLkro</recordid><startdate>20100815</startdate><enddate>20100815</enddate><creator>YANLEI GUAN</creator><creator>MIZOGUCHI, Masahiro</creator><creator>XINLONG MA</creator><creator>HAYASHI, Kenshi</creator><creator>SASAKI, Tomio</creator><creator>YOSHIMOTO, Koji</creator><creator>HATA, Nobuhiro</creator><creator>SHONO, Tadahisa</creator><creator>SUZUKI, Satoshi O</creator><creator>ARAKI, Yukie</creator><creator>KUGA, Daisuke</creator><creator>NAKAMIZO, Akira</creator><creator>AMANO, Toshiyuki</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><scope>7TK</scope></search><sort><creationdate>20100815</creationdate><title>MiRNA-196 Is Upregulated in Glioblastoma But Not in Anaplastic Astrocytoma and Has Prognostic Significance</title><author>YANLEI GUAN ; MIZOGUCHI, Masahiro ; XINLONG MA ; HAYASHI, Kenshi ; SASAKI, Tomio ; YOSHIMOTO, Koji ; HATA, Nobuhiro ; SHONO, Tadahisa ; SUZUKI, Satoshi O ; ARAKI, Yukie ; KUGA, Daisuke ; NAKAMIZO, Akira ; AMANO, Toshiyuki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c469t-463b0cb285be35ce313a464f08756e4ec70d6f2a7f7447efaba2e392db4c8aae3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Antineoplastic agents</topic><topic>Astrocytoma - genetics</topic><topic>Astrocytoma - mortality</topic><topic>Astrocytoma - pathology</topic><topic>Biological and medical sciences</topic><topic>Biomarkers, Tumor - genetics</topic><topic>Brain Neoplasms - genetics</topic><topic>Brain Neoplasms - mortality</topic><topic>Brain Neoplasms - pathology</topic><topic>Gene Expression</topic><topic>Gene Expression Profiling</topic><topic>Glioblastoma - genetics</topic><topic>Glioblastoma - mortality</topic><topic>Glioblastoma - pathology</topic><topic>Humans</topic><topic>Kaplan-Meier Estimate</topic><topic>Loss of Heterozygosity</topic><topic>Medical sciences</topic><topic>MicroRNAs - genetics</topic><topic>Microsatellite Repeats</topic><topic>Neurology</topic><topic>Pharmacology. Drug treatments</topic><topic>Prognosis</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>Tumors of the nervous system. Phacomatoses</topic><topic>Up-Regulation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>YANLEI GUAN</creatorcontrib><creatorcontrib>MIZOGUCHI, Masahiro</creatorcontrib><creatorcontrib>XINLONG MA</creatorcontrib><creatorcontrib>HAYASHI, Kenshi</creatorcontrib><creatorcontrib>SASAKI, Tomio</creatorcontrib><creatorcontrib>YOSHIMOTO, Koji</creatorcontrib><creatorcontrib>HATA, Nobuhiro</creatorcontrib><creatorcontrib>SHONO, Tadahisa</creatorcontrib><creatorcontrib>SUZUKI, Satoshi O</creatorcontrib><creatorcontrib>ARAKI, Yukie</creatorcontrib><creatorcontrib>KUGA, Daisuke</creatorcontrib><creatorcontrib>NAKAMIZO, Akira</creatorcontrib><creatorcontrib>AMANO, Toshiyuki</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><collection>Neurosciences Abstracts</collection><jtitle>Clinical cancer research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>YANLEI GUAN</au><au>MIZOGUCHI, Masahiro</au><au>XINLONG MA</au><au>HAYASHI, Kenshi</au><au>SASAKI, Tomio</au><au>YOSHIMOTO, Koji</au><au>HATA, Nobuhiro</au><au>SHONO, Tadahisa</au><au>SUZUKI, Satoshi O</au><au>ARAKI, Yukie</au><au>KUGA, Daisuke</au><au>NAKAMIZO, Akira</au><au>AMANO, Toshiyuki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>MiRNA-196 Is Upregulated in Glioblastoma But Not in Anaplastic Astrocytoma and Has Prognostic Significance</atitle><jtitle>Clinical cancer research</jtitle><addtitle>Clin Cancer Res</addtitle><date>2010-08-15</date><risdate>2010</risdate><volume>16</volume><issue>16</issue><spage>4289</spage><epage>4297</epage><pages>4289-4297</pages><issn>1078-0432</issn><eissn>1557-3265</eissn><coden>CCREF4</coden><abstract>MicroRNAs (miRNA) are short noncoding RNAs that can play critical roles in diverse biological processes. They are implicated in tumorigenesis and function both as tumor suppressors and as oncogenes. The clinical significance of miRNA expression profiles in malignant gliomas remains unclear.
In this study, we examined the expression levels of 365 mature human miRNAs in 12 malignant gliomas, including 8 glioblastomas and 4 anaplastic astrocytomas, using TaqMan real-time quantitative PCR arrays. A validation study was done to corroborate a subset of the results, including expression levels of miR-196a, -196b, -21, and -15b, by analyzing 92 malignant gliomas by conventional real-time PCR. We modeled the relationship between the expression levels of these miRNAs and the survival rate of 39 glioblastoma patients by Kaplan-Meier method and multivariate analysis.
Expression profiles in glioblastomas and anaplastic astrocytomas suggested that 16 miRNAs were candidate markers associated with the malignant progression of gliomas. Among them, miR-196a showed the most significant difference (P = 0.0038), with miR-196b also having a high significance (P = 0.0371). Both miRNAs showed increased expression levels in glioblastomas relative to both anaplastic astrocytomas and normal brains in the validation study. Furthermore, patients with high miR-196 expression levels showed significantly poorer survival by the Kaplan-Meier method (P = 0.0073). Multivariate analysis showed that miR-196 expression levels were an independent predictor of overall survival in all 39 glioblastoma patients (P = 0.021; hazard ratio, 2.81).
Our results suggest that miR-196 may play a role in the malignant progression of gliomas and may be a prognostic predictor in glioblastomas.</abstract><cop>Philadelphia, PA</cop><pub>American Association for Cancer Research</pub><pmid>20601442</pmid><doi>10.1158/1078-0432.CCR-10-0207</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Antineoplastic agents Astrocytoma - genetics Astrocytoma - mortality Astrocytoma - pathology Biological and medical sciences Biomarkers, Tumor - genetics Brain Neoplasms - genetics Brain Neoplasms - mortality Brain Neoplasms - pathology Gene Expression Gene Expression Profiling Glioblastoma - genetics Glioblastoma - mortality Glioblastoma - pathology Humans Kaplan-Meier Estimate Loss of Heterozygosity Medical sciences MicroRNAs - genetics Microsatellite Repeats Neurology Pharmacology. Drug treatments Prognosis Reverse Transcriptase Polymerase Chain Reaction Tumors of the nervous system. Phacomatoses Up-Regulation |
title | MiRNA-196 Is Upregulated in Glioblastoma But Not in Anaplastic Astrocytoma and Has Prognostic Significance |
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