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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Main Authors: Jialing Yuan, Tao Li, Ke Yi, Minmin Hou
Format: Article
Language:English
Published: Elsevier 2020-07-01
Series:Heliyon
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2405844020311026
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spelling 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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