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The suppressive role of miR-362-3p in epithelial ovarian cancer
Ovarian cancer is a common cancer worldwide. Epithelial ovarian cancer (EOC) is the most common subtype of ovarian cancer. This study was designed to explore the function of miR-362-3p in EOC. QRT-PCR analysis was used to test miR-362-3p levels in EOC tissues and cell lines. Cell viability was teste...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7347651/ https://www.ncbi.nlm.nih.gov/pubmed/32671239 http://dx.doi.org/10.1016/j.heliyon.2020.e04258 |
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author | Yuan, Jialing Li, Tao Yi, Ke Hou, Minmin |
author_facet | Yuan, Jialing Li, Tao Yi, Ke Hou, Minmin |
author_sort | Yuan, Jialing |
collection | PubMed |
description | Ovarian cancer is a common cancer worldwide. Epithelial ovarian cancer (EOC) is the most common subtype of ovarian cancer. This study was designed to explore the function of miR-362-3p in EOC. QRT-PCR analysis was used to test miR-362-3p levels in EOC tissues and cell lines. Cell viability was tested via MTT assay. Transwell systems were applied to assay cell migration. The target gene of miR-362-3p was evaluated using dual luciferase reporter assays. The MyD88 protein in EOC cells was tested via western blot. Our data showed that miR-362-3p was expressed at low levels in EOC tissues and cells. miR-362-3p inhibited cell proliferation and migration, bound the 3′-untranslated region (UTR) of MyD88, and inhibited MyD88 expression. MyD88 was inversely correlated with miR-362-3p in EOC, and MyD88 overexpression partly reduced the anti-proliferative effect of miR-362-3p in EOC cells. In conclusion, our data showed that miR-362-3p has an anti-proliferative effect on EOC. |
format | Online Article Text |
id | pubmed-7347651 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-73476512020-07-14 The suppressive role of miR-362-3p in epithelial ovarian cancer Yuan, Jialing Li, Tao Yi, Ke Hou, Minmin Heliyon Article Ovarian cancer is a common cancer worldwide. Epithelial ovarian cancer (EOC) is the most common subtype of ovarian cancer. This study was designed to explore the function of miR-362-3p in EOC. QRT-PCR analysis was used to test miR-362-3p levels in EOC tissues and cell lines. Cell viability was tested via MTT assay. Transwell systems were applied to assay cell migration. The target gene of miR-362-3p was evaluated using dual luciferase reporter assays. The MyD88 protein in EOC cells was tested via western blot. Our data showed that miR-362-3p was expressed at low levels in EOC tissues and cells. miR-362-3p inhibited cell proliferation and migration, bound the 3′-untranslated region (UTR) of MyD88, and inhibited MyD88 expression. MyD88 was inversely correlated with miR-362-3p in EOC, and MyD88 overexpression partly reduced the anti-proliferative effect of miR-362-3p in EOC cells. In conclusion, our data showed that miR-362-3p has an anti-proliferative effect on EOC. Elsevier 2020-07-07 /pmc/articles/PMC7347651/ /pubmed/32671239 http://dx.doi.org/10.1016/j.heliyon.2020.e04258 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Yuan, Jialing Li, Tao Yi, Ke Hou, Minmin The suppressive role of miR-362-3p in epithelial ovarian cancer |
title | The suppressive role of miR-362-3p in epithelial ovarian cancer |
title_full | The suppressive role of miR-362-3p in epithelial ovarian cancer |
title_fullStr | The suppressive role of miR-362-3p in epithelial ovarian cancer |
title_full_unstemmed | The suppressive role of miR-362-3p in epithelial ovarian cancer |
title_short | The suppressive role of miR-362-3p in epithelial ovarian cancer |
title_sort | suppressive role of mir-362-3p in epithelial ovarian cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7347651/ https://www.ncbi.nlm.nih.gov/pubmed/32671239 http://dx.doi.org/10.1016/j.heliyon.2020.e04258 |
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