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Circulating miR-182 is a biomarker of colorectal adenocarcinoma progression
MiR-182 expression was evaluated by qRT-PCR and in situ hybridization in 20 tubular adenomas, 50 colorectal carcinoma (CRC), and 40 CRC liver metastases. Control samples obtained from patients with irritable bowel syndrome, or tumor-matched normal colon mucosa were analyzed (n=50). MiR-182 expressio...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4196150/ https://www.ncbi.nlm.nih.gov/pubmed/25115394 |
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author | Perilli, Lisa Vicentini, Caterina Agostini, Marco Pizzini, Silvia Pizzi, Marco D'Angelo, Edoardo Bortoluzzi, Stefania Mandruzzato, Susanna Mammano, Enzo Rugge, Massimo Nitti, Donato Scarpa, Aldo Fassan, Matteo Zanovello, Paola |
author_facet | Perilli, Lisa Vicentini, Caterina Agostini, Marco Pizzini, Silvia Pizzi, Marco D'Angelo, Edoardo Bortoluzzi, Stefania Mandruzzato, Susanna Mammano, Enzo Rugge, Massimo Nitti, Donato Scarpa, Aldo Fassan, Matteo Zanovello, Paola |
author_sort | Perilli, Lisa |
collection | PubMed |
description | MiR-182 expression was evaluated by qRT-PCR and in situ hybridization in 20 tubular adenomas, 50 colorectal carcinoma (CRC), and 40 CRC liver metastases. Control samples obtained from patients with irritable bowel syndrome, or tumor-matched normal colon mucosa were analyzed (n=50). MiR-182 expression increased progressively and significantly along with the colorectal carcinogenesis cascade, and in CRC liver metastases. The inverse relation between miR-182 and the expression of its target gene ENTPD5 was investigated by immunohistochemical analysis. We observed that normal colocytes featured a strong ENTPD5 cytoplasmic expression whereas a significantly and progressively lower expression was present along with dedifferentiation of the histologic phenotype. Plasma samples from 51 CRC patients and controls were tested for miR-182 expression. Plasma miR-182 concentrations were significantly higher in CRC patients than in healthy controls or patients with colon polyps at endoscopy. Moreover, miR-182 plasma levels were significantly reduced in post-operative samples after radical hepatic metastasectomy compared to preoperative samples. Our results strengthen the hypothesis of a central role of miR-182 dysregulation in colon mucosa transformation, demonstrate the concomitant progressive down-regulation of ENTPD5 levels during colon carcinogenesis, and indicate the potential of circulating miR-182 as blood based biomarker for screening and monitoring CRC during the follow-up. |
format | Online Article Text |
id | pubmed-4196150 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-41961502014-10-21 Circulating miR-182 is a biomarker of colorectal adenocarcinoma progression Perilli, Lisa Vicentini, Caterina Agostini, Marco Pizzini, Silvia Pizzi, Marco D'Angelo, Edoardo Bortoluzzi, Stefania Mandruzzato, Susanna Mammano, Enzo Rugge, Massimo Nitti, Donato Scarpa, Aldo Fassan, Matteo Zanovello, Paola Oncotarget Clinical Research Paper MiR-182 expression was evaluated by qRT-PCR and in situ hybridization in 20 tubular adenomas, 50 colorectal carcinoma (CRC), and 40 CRC liver metastases. Control samples obtained from patients with irritable bowel syndrome, or tumor-matched normal colon mucosa were analyzed (n=50). MiR-182 expression increased progressively and significantly along with the colorectal carcinogenesis cascade, and in CRC liver metastases. The inverse relation between miR-182 and the expression of its target gene ENTPD5 was investigated by immunohistochemical analysis. We observed that normal colocytes featured a strong ENTPD5 cytoplasmic expression whereas a significantly and progressively lower expression was present along with dedifferentiation of the histologic phenotype. Plasma samples from 51 CRC patients and controls were tested for miR-182 expression. Plasma miR-182 concentrations were significantly higher in CRC patients than in healthy controls or patients with colon polyps at endoscopy. Moreover, miR-182 plasma levels were significantly reduced in post-operative samples after radical hepatic metastasectomy compared to preoperative samples. Our results strengthen the hypothesis of a central role of miR-182 dysregulation in colon mucosa transformation, demonstrate the concomitant progressive down-regulation of ENTPD5 levels during colon carcinogenesis, and indicate the potential of circulating miR-182 as blood based biomarker for screening and monitoring CRC during the follow-up. Impact Journals LLC 2014-07-23 /pmc/articles/PMC4196150/ /pubmed/25115394 Text en Copyright: © 2014 Perilli et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Clinical Research Paper Perilli, Lisa Vicentini, Caterina Agostini, Marco Pizzini, Silvia Pizzi, Marco D'Angelo, Edoardo Bortoluzzi, Stefania Mandruzzato, Susanna Mammano, Enzo Rugge, Massimo Nitti, Donato Scarpa, Aldo Fassan, Matteo Zanovello, Paola Circulating miR-182 is a biomarker of colorectal adenocarcinoma progression |
title | Circulating miR-182 is a biomarker of colorectal adenocarcinoma progression |
title_full | Circulating miR-182 is a biomarker of colorectal adenocarcinoma progression |
title_fullStr | Circulating miR-182 is a biomarker of colorectal adenocarcinoma progression |
title_full_unstemmed | Circulating miR-182 is a biomarker of colorectal adenocarcinoma progression |
title_short | Circulating miR-182 is a biomarker of colorectal adenocarcinoma progression |
title_sort | circulating mir-182 is a biomarker of colorectal adenocarcinoma progression |
topic | Clinical Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4196150/ https://www.ncbi.nlm.nih.gov/pubmed/25115394 |
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