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MicroRNAs Targeting Caspase-3 and -7 in PANC-1 Cells
MicroRNAs (miRNAs), a critical part of the RNA silencing machinery, are known to play important regulatory roles in cancer. However, the consequence of miRNA deregulation in cancer is unknown for many miRNAs. Here, we define that miRNAs, miR-17-5p, miR-132-3p/-212-3p, and miR-337-3p are significantl...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5979519/ https://www.ncbi.nlm.nih.gov/pubmed/29659498 http://dx.doi.org/10.3390/ijms19041206 |
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author | Park, Jong Kook Doseff, Andrea I. Schmittgen, Thomas D. |
author_facet | Park, Jong Kook Doseff, Andrea I. Schmittgen, Thomas D. |
author_sort | Park, Jong Kook |
collection | PubMed |
description | MicroRNAs (miRNAs), a critical part of the RNA silencing machinery, are known to play important regulatory roles in cancer. However, the consequence of miRNA deregulation in cancer is unknown for many miRNAs. Here, we define that miRNAs, miR-17-5p, miR-132-3p/-212-3p, and miR-337-3p are significantly up-regulated in the pancreatic ductal adenocarcinomas (PDAC) compared to the normal and benign tissues. Furthermore, by using PANC-1 cells, we demonstrate that overexpressed miR-337-3p and miR-17-5p/miR-132-3p/-212-3p can regulate executioner caspases-3 and -7, respectively. In addition, over-expression of miRNAs, especially miR-337-3p, attenuates tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) cytotoxicity in PANC-1 cells. Our findings unveil an important biological function for miRNAs up-regulated in PDAC in coordinately regulating caspases, potentially contributing to the malignant progression of PDAC. |
format | Online Article Text |
id | pubmed-5979519 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-59795192018-06-10 MicroRNAs Targeting Caspase-3 and -7 in PANC-1 Cells Park, Jong Kook Doseff, Andrea I. Schmittgen, Thomas D. Int J Mol Sci Article MicroRNAs (miRNAs), a critical part of the RNA silencing machinery, are known to play important regulatory roles in cancer. However, the consequence of miRNA deregulation in cancer is unknown for many miRNAs. Here, we define that miRNAs, miR-17-5p, miR-132-3p/-212-3p, and miR-337-3p are significantly up-regulated in the pancreatic ductal adenocarcinomas (PDAC) compared to the normal and benign tissues. Furthermore, by using PANC-1 cells, we demonstrate that overexpressed miR-337-3p and miR-17-5p/miR-132-3p/-212-3p can regulate executioner caspases-3 and -7, respectively. In addition, over-expression of miRNAs, especially miR-337-3p, attenuates tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) cytotoxicity in PANC-1 cells. Our findings unveil an important biological function for miRNAs up-regulated in PDAC in coordinately regulating caspases, potentially contributing to the malignant progression of PDAC. MDPI 2018-04-16 /pmc/articles/PMC5979519/ /pubmed/29659498 http://dx.doi.org/10.3390/ijms19041206 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Park, Jong Kook Doseff, Andrea I. Schmittgen, Thomas D. MicroRNAs Targeting Caspase-3 and -7 in PANC-1 Cells |
title | MicroRNAs Targeting Caspase-3 and -7 in PANC-1 Cells |
title_full | MicroRNAs Targeting Caspase-3 and -7 in PANC-1 Cells |
title_fullStr | MicroRNAs Targeting Caspase-3 and -7 in PANC-1 Cells |
title_full_unstemmed | MicroRNAs Targeting Caspase-3 and -7 in PANC-1 Cells |
title_short | MicroRNAs Targeting Caspase-3 and -7 in PANC-1 Cells |
title_sort | micrornas targeting caspase-3 and -7 in panc-1 cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5979519/ https://www.ncbi.nlm.nih.gov/pubmed/29659498 http://dx.doi.org/10.3390/ijms19041206 |
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