mRNA/microRNA gene expression profile in microsatellite unstable colorectal cancer

<p>Abstract</p> <p>Background</p> <p>Colorectal cancer develops through two main genetic instability pathways characterized by distinct pathologic features and clinical outcome.</p> <p>Results</p> <p>We investigated colon cancer samples (23 chara...

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Main Authors: Calin George A, Liu Chang-gong, Pichiorri Flavia, Spizzo Riccardo, Veronese Angelo, Gafà Roberta, Ferracin Manuela, Lanza Giovanni, Croce Carlo M, Negrini Massimo
Format: Article
Language:English
Published: BMC 2007-08-01
Series:Molecular Cancer
Online Access:http://www.molecular-cancer.com/content/6/1/54
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spelling doaj-1c6d17d0f8e2417b9aa43687559d1d892020-11-24T21:52:39ZengBMCMolecular Cancer1476-45982007-08-01615410.1186/1476-4598-6-54mRNA/microRNA gene expression profile in microsatellite unstable colorectal cancerCalin George ALiu Chang-gongPichiorri FlaviaSpizzo RiccardoVeronese AngeloGafà RobertaFerracin ManuelaLanza GiovanniCroce Carlo MNegrini Massimo<p>Abstract</p> <p>Background</p> <p>Colorectal cancer develops through two main genetic instability pathways characterized by distinct pathologic features and clinical outcome.</p> <p>Results</p> <p>We investigated colon cancer samples (23 characterized by microsatellite stability, MSS, and 16 by high microsatellite instability, MSI-H) for genome-wide expression of microRNA (miRNA) and mRNA. Based on combined miRNA and mRNA gene expression, a molecular signature consisting of twenty seven differentially expressed genes, inclusive of 8 miRNAs, could correctly distinguish MSI-H versus MSS colon cancer samples. Among the differentially expressed miRNAs, various members of the oncogenic miR-17-92 family were significantly up-regulated in MSS cancers. The majority of protein coding genes were also up-regulated in MSS cancers. Their functional classification revealed that they were most frequently associated with cell cycle, DNA replication, recombination, repair, gastrointestinal disease and immune response.</p> <p>Conclusion</p> <p>This is the first report that indicates the existence of differences in miRNA expression between MSS versus MSI-H colorectal cancers. In addition, the work suggests that the combination of mRNA/miRNA expression signatures may represent a general approach for improving bio-molecular classification of human cancer.</p> http://www.molecular-cancer.com/content/6/1/54
collection DOAJ
language English
format Article
sources DOAJ
author Calin George A
Liu Chang-gong
Pichiorri Flavia
Spizzo Riccardo
Veronese Angelo
Gafà Roberta
Ferracin Manuela
Lanza Giovanni
Croce Carlo M
Negrini Massimo
spellingShingle Calin George A
Liu Chang-gong
Pichiorri Flavia
Spizzo Riccardo
Veronese Angelo
Gafà Roberta
Ferracin Manuela
Lanza Giovanni
Croce Carlo M
Negrini Massimo
mRNA/microRNA gene expression profile in microsatellite unstable colorectal cancer
Molecular Cancer
author_facet Calin George A
Liu Chang-gong
Pichiorri Flavia
Spizzo Riccardo
Veronese Angelo
Gafà Roberta
Ferracin Manuela
Lanza Giovanni
Croce Carlo M
Negrini Massimo
author_sort Calin George A
title mRNA/microRNA gene expression profile in microsatellite unstable colorectal cancer
title_short mRNA/microRNA gene expression profile in microsatellite unstable colorectal cancer
title_full mRNA/microRNA gene expression profile in microsatellite unstable colorectal cancer
title_fullStr mRNA/microRNA gene expression profile in microsatellite unstable colorectal cancer
title_full_unstemmed mRNA/microRNA gene expression profile in microsatellite unstable colorectal cancer
title_sort mrna/microrna gene expression profile in microsatellite unstable colorectal cancer
publisher BMC
series Molecular Cancer
issn 1476-4598
publishDate 2007-08-01
description <p>Abstract</p> <p>Background</p> <p>Colorectal cancer develops through two main genetic instability pathways characterized by distinct pathologic features and clinical outcome.</p> <p>Results</p> <p>We investigated colon cancer samples (23 characterized by microsatellite stability, MSS, and 16 by high microsatellite instability, MSI-H) for genome-wide expression of microRNA (miRNA) and mRNA. Based on combined miRNA and mRNA gene expression, a molecular signature consisting of twenty seven differentially expressed genes, inclusive of 8 miRNAs, could correctly distinguish MSI-H versus MSS colon cancer samples. Among the differentially expressed miRNAs, various members of the oncogenic miR-17-92 family were significantly up-regulated in MSS cancers. The majority of protein coding genes were also up-regulated in MSS cancers. Their functional classification revealed that they were most frequently associated with cell cycle, DNA replication, recombination, repair, gastrointestinal disease and immune response.</p> <p>Conclusion</p> <p>This is the first report that indicates the existence of differences in miRNA expression between MSS versus MSI-H colorectal cancers. In addition, the work suggests that the combination of mRNA/miRNA expression signatures may represent a general approach for improving bio-molecular classification of human cancer.</p>
url http://www.molecular-cancer.com/content/6/1/54
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