Cargando…
The miR-196b miRNA inhibits the GATA6 intestinal transcription factor and is upregulated in colon cancer patients
OBJECTIVE: To explore the possible misexpression of the microRNA miR-196b in colorectal cancer (CRC) and its role in controlling the expression of GATA6, a putative target gene crucial to intestinal cell homeostasis and tumorigenesis. DESIGN: The expression of miR-196b was analysed by qRT-PCR in sur...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5354868/ https://www.ncbi.nlm.nih.gov/pubmed/27902469 http://dx.doi.org/10.18632/oncotarget.13580 |
_version_ | 1782515414981410816 |
---|---|
author | Fantini, Sebastian Salsi, Valentina Reggiani, Luca Maiorana, Antonino Zappavigna, Vincenzo |
author_facet | Fantini, Sebastian Salsi, Valentina Reggiani, Luca Maiorana, Antonino Zappavigna, Vincenzo |
author_sort | Fantini, Sebastian |
collection | PubMed |
description | OBJECTIVE: To explore the possible misexpression of the microRNA miR-196b in colorectal cancer (CRC) and its role in controlling the expression of GATA6, a putative target gene crucial to intestinal cell homeostasis and tumorigenesis. DESIGN: The expression of miR-196b was analysed by qRT-PCR in surgical resection samples from a cohort of sporadic colon cancer patients. Manipulations of miR-196b expression were performed to demonstrate its inhibition of GATA6 protein levels. RESULTS: We found that miR-196b is significantly upregulated in pre-treatment surgical resection samples from a cohort of sporadic colon cancer patients. The upregulation of miR-196b correlates with less severe clinicopathological characteristics, such as early tumor stage and absence of lymph node metastases. We show that in CRC cells, miR-196b targets the mRNA of GATA6, a transcription factor involved in the homeostasis and differentiation of intestinal epithelial cells, and a positive regulator of the Wnt/β-catenin pathway. We moreover found that the increase of miR-196b correlates with a reduced GATA6 protein expression in colon cancer patients. CONCLUSION: Our results establish miR-196b as a post-transcriptional inhibitor of GATA6 in CRC cells, implicating miR-196b function in gene regulatory pathways crucial to intestinal cell homeostasis and tumorigenesis. Our results furthermore suggest a role of miR-196b expression in CRC, as an antagonist of GATA6 function in tumor cells, thus providing the basis for a potential targeting strategy for the treatment of CRC. |
format | Online Article Text |
id | pubmed-5354868 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-53548682017-04-24 The miR-196b miRNA inhibits the GATA6 intestinal transcription factor and is upregulated in colon cancer patients Fantini, Sebastian Salsi, Valentina Reggiani, Luca Maiorana, Antonino Zappavigna, Vincenzo Oncotarget Research Paper OBJECTIVE: To explore the possible misexpression of the microRNA miR-196b in colorectal cancer (CRC) and its role in controlling the expression of GATA6, a putative target gene crucial to intestinal cell homeostasis and tumorigenesis. DESIGN: The expression of miR-196b was analysed by qRT-PCR in surgical resection samples from a cohort of sporadic colon cancer patients. Manipulations of miR-196b expression were performed to demonstrate its inhibition of GATA6 protein levels. RESULTS: We found that miR-196b is significantly upregulated in pre-treatment surgical resection samples from a cohort of sporadic colon cancer patients. The upregulation of miR-196b correlates with less severe clinicopathological characteristics, such as early tumor stage and absence of lymph node metastases. We show that in CRC cells, miR-196b targets the mRNA of GATA6, a transcription factor involved in the homeostasis and differentiation of intestinal epithelial cells, and a positive regulator of the Wnt/β-catenin pathway. We moreover found that the increase of miR-196b correlates with a reduced GATA6 protein expression in colon cancer patients. CONCLUSION: Our results establish miR-196b as a post-transcriptional inhibitor of GATA6 in CRC cells, implicating miR-196b function in gene regulatory pathways crucial to intestinal cell homeostasis and tumorigenesis. Our results furthermore suggest a role of miR-196b expression in CRC, as an antagonist of GATA6 function in tumor cells, thus providing the basis for a potential targeting strategy for the treatment of CRC. Impact Journals LLC 2016-11-25 /pmc/articles/PMC5354868/ /pubmed/27902469 http://dx.doi.org/10.18632/oncotarget.13580 Text en Copyright: © 2017 Fantini et al. http://creativecommons.org/licenses/by/3.0/ 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 | Research Paper Fantini, Sebastian Salsi, Valentina Reggiani, Luca Maiorana, Antonino Zappavigna, Vincenzo The miR-196b miRNA inhibits the GATA6 intestinal transcription factor and is upregulated in colon cancer patients |
title | The miR-196b miRNA inhibits the GATA6 intestinal transcription factor and is upregulated in colon cancer patients |
title_full | The miR-196b miRNA inhibits the GATA6 intestinal transcription factor and is upregulated in colon cancer patients |
title_fullStr | The miR-196b miRNA inhibits the GATA6 intestinal transcription factor and is upregulated in colon cancer patients |
title_full_unstemmed | The miR-196b miRNA inhibits the GATA6 intestinal transcription factor and is upregulated in colon cancer patients |
title_short | The miR-196b miRNA inhibits the GATA6 intestinal transcription factor and is upregulated in colon cancer patients |
title_sort | mir-196b mirna inhibits the gata6 intestinal transcription factor and is upregulated in colon cancer patients |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5354868/ https://www.ncbi.nlm.nih.gov/pubmed/27902469 http://dx.doi.org/10.18632/oncotarget.13580 |
work_keys_str_mv | AT fantinisebastian themir196bmirnainhibitsthegata6intestinaltranscriptionfactorandisupregulatedincoloncancerpatients AT salsivalentina themir196bmirnainhibitsthegata6intestinaltranscriptionfactorandisupregulatedincoloncancerpatients AT reggianiluca themir196bmirnainhibitsthegata6intestinaltranscriptionfactorandisupregulatedincoloncancerpatients AT maioranaantonino themir196bmirnainhibitsthegata6intestinaltranscriptionfactorandisupregulatedincoloncancerpatients AT zappavignavincenzo themir196bmirnainhibitsthegata6intestinaltranscriptionfactorandisupregulatedincoloncancerpatients AT fantinisebastian mir196bmirnainhibitsthegata6intestinaltranscriptionfactorandisupregulatedincoloncancerpatients AT salsivalentina mir196bmirnainhibitsthegata6intestinaltranscriptionfactorandisupregulatedincoloncancerpatients AT reggianiluca mir196bmirnainhibitsthegata6intestinaltranscriptionfactorandisupregulatedincoloncancerpatients AT maioranaantonino mir196bmirnainhibitsthegata6intestinaltranscriptionfactorandisupregulatedincoloncancerpatients AT zappavignavincenzo mir196bmirnainhibitsthegata6intestinaltranscriptionfactorandisupregulatedincoloncancerpatients |