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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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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