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Induction of miR-3648 Upon ER Stress and Its Regulatory Role in Cell Proliferation
MicroRNAs (miRNAs) play important roles under multiple cellular conditions including endoplasmic reticulum (ER) stress. We found that miR-3648, a human specific microRNA, was induced under ER stress. Moreover, Adenomatous polyposis coli 2 (APC2), a tumor suppressor and a negative regulator of Wnt si...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5535868/ https://www.ncbi.nlm.nih.gov/pubmed/28661420 http://dx.doi.org/10.3390/ijms18071375 |
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author | Rashid, Farooq Awan, Hassaan Mehboob Shah, Abdullah Chen, Liang Shan, Ge |
author_facet | Rashid, Farooq Awan, Hassaan Mehboob Shah, Abdullah Chen, Liang Shan, Ge |
author_sort | Rashid, Farooq |
collection | PubMed |
description | MicroRNAs (miRNAs) play important roles under multiple cellular conditions including endoplasmic reticulum (ER) stress. We found that miR-3648, a human specific microRNA, was induced under ER stress. Moreover, Adenomatous polyposis coli 2 (APC2), a tumor suppressor and a negative regulator of Wnt signaling, was found to be the direct target of miR-3648. Levels of APC2 were downregulated when cells were under ER stress or after overexpressing miR-3648. Inhibition of miR-3648 by antagomir increased APC2 levels and decreased cell proliferation. Conversely, when miR-3648 was overexpressed, APC2 levels were decreased and the cell growth increased. Our data demonstrated that ER stress mediated induction of miR-3648 in human cells, which then downregulated APC2 to increase cell proliferation. |
format | Online Article Text |
id | pubmed-5535868 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-55358682017-08-04 Induction of miR-3648 Upon ER Stress and Its Regulatory Role in Cell Proliferation Rashid, Farooq Awan, Hassaan Mehboob Shah, Abdullah Chen, Liang Shan, Ge Int J Mol Sci Article MicroRNAs (miRNAs) play important roles under multiple cellular conditions including endoplasmic reticulum (ER) stress. We found that miR-3648, a human specific microRNA, was induced under ER stress. Moreover, Adenomatous polyposis coli 2 (APC2), a tumor suppressor and a negative regulator of Wnt signaling, was found to be the direct target of miR-3648. Levels of APC2 were downregulated when cells were under ER stress or after overexpressing miR-3648. Inhibition of miR-3648 by antagomir increased APC2 levels and decreased cell proliferation. Conversely, when miR-3648 was overexpressed, APC2 levels were decreased and the cell growth increased. Our data demonstrated that ER stress mediated induction of miR-3648 in human cells, which then downregulated APC2 to increase cell proliferation. MDPI 2017-06-29 /pmc/articles/PMC5535868/ /pubmed/28661420 http://dx.doi.org/10.3390/ijms18071375 Text en © 2017 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 Rashid, Farooq Awan, Hassaan Mehboob Shah, Abdullah Chen, Liang Shan, Ge Induction of miR-3648 Upon ER Stress and Its Regulatory Role in Cell Proliferation |
title | Induction of miR-3648 Upon ER Stress and Its Regulatory Role in Cell Proliferation |
title_full | Induction of miR-3648 Upon ER Stress and Its Regulatory Role in Cell Proliferation |
title_fullStr | Induction of miR-3648 Upon ER Stress and Its Regulatory Role in Cell Proliferation |
title_full_unstemmed | Induction of miR-3648 Upon ER Stress and Its Regulatory Role in Cell Proliferation |
title_short | Induction of miR-3648 Upon ER Stress and Its Regulatory Role in Cell Proliferation |
title_sort | induction of mir-3648 upon er stress and its regulatory role in cell proliferation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5535868/ https://www.ncbi.nlm.nih.gov/pubmed/28661420 http://dx.doi.org/10.3390/ijms18071375 |
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