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...
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doaj-9a9878e34e314e32b2060a23b6a1c8362020-11-25T03:07:54ZengElsevierHeliyon2405-84402020-07-0167e04258The suppressive role of miR-362-3p in epithelial ovarian cancerJialing Yuan0Tao Li1Ke Yi2Minmin Hou3Key Laboratory of Birth Defects and Related Diseases of Women and Children (Sichuan University), Ministry of Education, ChinaKey Laboratory of Birth Defects and Related Diseases of Women and Children (Sichuan University), Ministry of Education, ChinaKey Laboratory of Birth Defects and Related Diseases of Women and Children (Sichuan University), Ministry of Education, ChinaCorresponding author.; Key Laboratory of Birth Defects and Related Diseases of Women and Children (Sichuan University), Ministry of Education, ChinaOvarian 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.http://www.sciencedirect.com/science/article/pii/S2405844020311026Cell biologyBioinformaticsCancer researchOncologyClinical researchOvarian cancer |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Jialing Yuan Tao Li Ke Yi Minmin Hou |
spellingShingle |
Jialing Yuan Tao Li Ke Yi Minmin Hou The suppressive role of miR-362-3p in epithelial ovarian cancer Heliyon Cell biology Bioinformatics Cancer research Oncology Clinical research Ovarian cancer |
author_facet |
Jialing Yuan Tao Li Ke Yi Minmin Hou |
author_sort |
Jialing Yuan |
title |
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_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_sort |
suppressive role of mir-362-3p in epithelial ovarian cancer |
publisher |
Elsevier |
series |
Heliyon |
issn |
2405-8440 |
publishDate |
2020-07-01 |
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. |
topic |
Cell biology Bioinformatics Cancer research Oncology Clinical research Ovarian cancer |
url |
http://www.sciencedirect.com/science/article/pii/S2405844020311026 |
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