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An essential microRNA maturing microprocessor complex component DGCR8 is up-regulated in colorectal carcinomas
MicroRNAs (miRNAs) regulate gene expression through degradation and/or translational repression of target mRNAs. Dysregulations in the miRNA machinery may be involved in carcinogenesis of colorectal cancer (CRC). The purpose of the current study was to evaluate the DiGeorge syndrome critical region...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Milan
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4113675/ https://www.ncbi.nlm.nih.gov/pubmed/23775303 http://dx.doi.org/10.1007/s10238-013-0243-8 |
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author | Kim, Bora Lee, Jae-ho Park, Jong Wook Kwon, Taeg Kyu Baek, Seong Kyu Hwang, Ilseon Kim, Shin |
author_facet | Kim, Bora Lee, Jae-ho Park, Jong Wook Kwon, Taeg Kyu Baek, Seong Kyu Hwang, Ilseon Kim, Shin |
author_sort | Kim, Bora |
collection | PubMed |
description | MicroRNAs (miRNAs) regulate gene expression through degradation and/or translational repression of target mRNAs. Dysregulations in the miRNA machinery may be involved in carcinogenesis of colorectal cancer (CRC). The purpose of the current study was to evaluate the DiGeorge syndrome critical region gene 8 (DGCR8) and argonaute 2 (AGO2) mRNA expression in CRC and to evaluate the value of clinical parameters on their expression. We investigated the mRNA expressions of DGCR8 and AGO2 in 60 CRC tissues and adjacent histologically non-neoplastic tissues by using quantitative real-time PCR. Our study revealed that the mRNA expression level of DGCR8 is up-regulated in CRC. However, AGO2 mRNA expression was not significantly altered in CRC tissues. Neither DGCR8 nor AGO2 mRNA expression level was not associated with any clinical parameters, including age, tumor stage, CEA titer, and BMI in CRC cases. However, the mRNA expression levels of DGCR8 and AGO2 were positively correlated to each other. This study demonstrated for the first time that the DGCR8 mRNA expression level was up-regulated in CRC, suggesting its important role in pathobiology of colorectal carcinogenesis. |
format | Online Article Text |
id | pubmed-4113675 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Springer Milan |
record_format | MEDLINE/PubMed |
spelling | pubmed-41136752014-07-30 An essential microRNA maturing microprocessor complex component DGCR8 is up-regulated in colorectal carcinomas Kim, Bora Lee, Jae-ho Park, Jong Wook Kwon, Taeg Kyu Baek, Seong Kyu Hwang, Ilseon Kim, Shin Clin Exp Med Original Article MicroRNAs (miRNAs) regulate gene expression through degradation and/or translational repression of target mRNAs. Dysregulations in the miRNA machinery may be involved in carcinogenesis of colorectal cancer (CRC). The purpose of the current study was to evaluate the DiGeorge syndrome critical region gene 8 (DGCR8) and argonaute 2 (AGO2) mRNA expression in CRC and to evaluate the value of clinical parameters on their expression. We investigated the mRNA expressions of DGCR8 and AGO2 in 60 CRC tissues and adjacent histologically non-neoplastic tissues by using quantitative real-time PCR. Our study revealed that the mRNA expression level of DGCR8 is up-regulated in CRC. However, AGO2 mRNA expression was not significantly altered in CRC tissues. Neither DGCR8 nor AGO2 mRNA expression level was not associated with any clinical parameters, including age, tumor stage, CEA titer, and BMI in CRC cases. However, the mRNA expression levels of DGCR8 and AGO2 were positively correlated to each other. This study demonstrated for the first time that the DGCR8 mRNA expression level was up-regulated in CRC, suggesting its important role in pathobiology of colorectal carcinogenesis. Springer Milan 2013-06-18 2014 /pmc/articles/PMC4113675/ /pubmed/23775303 http://dx.doi.org/10.1007/s10238-013-0243-8 Text en © The Author(s) 2013 https://creativecommons.org/licenses/by/2.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Original Article Kim, Bora Lee, Jae-ho Park, Jong Wook Kwon, Taeg Kyu Baek, Seong Kyu Hwang, Ilseon Kim, Shin An essential microRNA maturing microprocessor complex component DGCR8 is up-regulated in colorectal carcinomas |
title | An essential microRNA maturing microprocessor complex component DGCR8 is up-regulated in colorectal carcinomas |
title_full | An essential microRNA maturing microprocessor complex component DGCR8 is up-regulated in colorectal carcinomas |
title_fullStr | An essential microRNA maturing microprocessor complex component DGCR8 is up-regulated in colorectal carcinomas |
title_full_unstemmed | An essential microRNA maturing microprocessor complex component DGCR8 is up-regulated in colorectal carcinomas |
title_short | An essential microRNA maturing microprocessor complex component DGCR8 is up-regulated in colorectal carcinomas |
title_sort | essential microrna maturing microprocessor complex component dgcr8 is up-regulated in colorectal carcinomas |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4113675/ https://www.ncbi.nlm.nih.gov/pubmed/23775303 http://dx.doi.org/10.1007/s10238-013-0243-8 |
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