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Identification by Real-time PCR of 13 mature microRNAs differentially expressed in colorectal cancer and non-tumoral tissues

MicroRNAs (miRNAs) are short non-coding RNA molecules playing regulatory roles by repressing translation or cleaving RNA transcripts. Although the number of verified human miRNA is still expanding, only few have been functionally described. However, emerging evidences suggest the potential involveme...

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Autores principales: Bandrés, E, Cubedo, E, Agirre, X, Malumbres, R, Zárate, R, Ramirez, N, Abajo, A, Navarro, A, Moreno, I, Monzó, M, García-Foncillas, J
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1550420/
https://www.ncbi.nlm.nih.gov/pubmed/16854228
http://dx.doi.org/10.1186/1476-4598-5-29
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author Bandrés, E
Cubedo, E
Agirre, X
Malumbres, R
Zárate, R
Ramirez, N
Abajo, A
Navarro, A
Moreno, I
Monzó, M
García-Foncillas, J
author_facet Bandrés, E
Cubedo, E
Agirre, X
Malumbres, R
Zárate, R
Ramirez, N
Abajo, A
Navarro, A
Moreno, I
Monzó, M
García-Foncillas, J
author_sort Bandrés, E
collection PubMed
description MicroRNAs (miRNAs) are short non-coding RNA molecules playing regulatory roles by repressing translation or cleaving RNA transcripts. Although the number of verified human miRNA is still expanding, only few have been functionally described. However, emerging evidences suggest the potential involvement of altered regulation of miRNA in pathogenesis of cancers and these genes are thought to function as both tumours suppressor and oncogenes. In our study, we examined by Real-Time PCR the expression of 156 mature miRNA in colorectal cancer. The analysis by several bioinformatics algorithms of colorectal tumours and adjacent non-neoplastic tissues from patients and colorectal cancer cell lines allowed identifying a group of 13 miRNA whose expression is significantly altered in this tumor. The most significantly deregulated miRNA being miR-31, miR-96, miR-133b, miR-135b, miR-145, and miR-183. In addition, the expression level of miR-31 was correlated with the stage of CRC tumor. Our results suggest that miRNA expression profile could have relevance to the biological and clinical behavior of colorectal neoplasia.
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spelling pubmed-15504202006-08-18 Identification by Real-time PCR of 13 mature microRNAs differentially expressed in colorectal cancer and non-tumoral tissues Bandrés, E Cubedo, E Agirre, X Malumbres, R Zárate, R Ramirez, N Abajo, A Navarro, A Moreno, I Monzó, M García-Foncillas, J Mol Cancer Research MicroRNAs (miRNAs) are short non-coding RNA molecules playing regulatory roles by repressing translation or cleaving RNA transcripts. Although the number of verified human miRNA is still expanding, only few have been functionally described. However, emerging evidences suggest the potential involvement of altered regulation of miRNA in pathogenesis of cancers and these genes are thought to function as both tumours suppressor and oncogenes. In our study, we examined by Real-Time PCR the expression of 156 mature miRNA in colorectal cancer. The analysis by several bioinformatics algorithms of colorectal tumours and adjacent non-neoplastic tissues from patients and colorectal cancer cell lines allowed identifying a group of 13 miRNA whose expression is significantly altered in this tumor. The most significantly deregulated miRNA being miR-31, miR-96, miR-133b, miR-135b, miR-145, and miR-183. In addition, the expression level of miR-31 was correlated with the stage of CRC tumor. Our results suggest that miRNA expression profile could have relevance to the biological and clinical behavior of colorectal neoplasia. BioMed Central 2006-07-19 /pmc/articles/PMC1550420/ /pubmed/16854228 http://dx.doi.org/10.1186/1476-4598-5-29 Text en Copyright © 2006 Bandrés et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Bandrés, E
Cubedo, E
Agirre, X
Malumbres, R
Zárate, R
Ramirez, N
Abajo, A
Navarro, A
Moreno, I
Monzó, M
García-Foncillas, J
Identification by Real-time PCR of 13 mature microRNAs differentially expressed in colorectal cancer and non-tumoral tissues
title Identification by Real-time PCR of 13 mature microRNAs differentially expressed in colorectal cancer and non-tumoral tissues
title_full Identification by Real-time PCR of 13 mature microRNAs differentially expressed in colorectal cancer and non-tumoral tissues
title_fullStr Identification by Real-time PCR of 13 mature microRNAs differentially expressed in colorectal cancer and non-tumoral tissues
title_full_unstemmed Identification by Real-time PCR of 13 mature microRNAs differentially expressed in colorectal cancer and non-tumoral tissues
title_short Identification by Real-time PCR of 13 mature microRNAs differentially expressed in colorectal cancer and non-tumoral tissues
title_sort identification by real-time pcr of 13 mature micrornas differentially expressed in colorectal cancer and non-tumoral tissues
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1550420/
https://www.ncbi.nlm.nih.gov/pubmed/16854228
http://dx.doi.org/10.1186/1476-4598-5-29
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