LncRNA miR503HG interacts with miR-31-5p through multiple ways to regulate cancer cell invasion and migration in ovarian cancer

Abstract The role of lncRNA miR503HG has been investigated in several types of cancer, but its functions in ovarian cancer (OC) is unclear. Analysis of TCGA dataset revealed a 50-fold lower expression level of miR503HG in OC tissues than that in non-tumor tissues, indicating the involvement of miR50...

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Main Authors: Ding Zhu, Xueshuang Huang, Fang Liang, Lijing Zhao
Format: Article
Language:English
Published: BMC 2020-01-01
Series:Journal of Ovarian Research
Subjects:
Online Access:https://doi.org/10.1186/s13048-019-0599-9
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spelling doaj-4a5b707291a3439fa57f3252d85986802021-01-10T12:40:21ZengBMCJournal of Ovarian Research1757-22152020-01-011311710.1186/s13048-019-0599-9LncRNA miR503HG interacts with miR-31-5p through multiple ways to regulate cancer cell invasion and migration in ovarian cancerDing Zhu0Xueshuang Huang1Fang Liang2Lijing Zhao3Department of Gynecology, Hunan Provincial People’s HospitalBiomedical Research Center, Hunan University of MedicineDepartment of Gynecology, Hunan Provincial People’s HospitalDepartment of Gynecology, Hunan Provincial People’s HospitalAbstract The role of lncRNA miR503HG has been investigated in several types of cancer, but its functions in ovarian cancer (OC) is unclear. Analysis of TCGA dataset revealed a 50-fold lower expression level of miR503HG in OC tissues than that in non-tumor tissues, indicating the involvement of miR503HG in OC. Results in this study showed that miR503HG was downregulated in OC and predicted poor survival. Expression of miR503HG negatively correlated with the expression of miR-31-5p across OC and non-tumor tissues. RNA-RNA interaction analysis revealed that miR503HG can interact with miR-31-5p. Dual-luciferase assay showed that miR-31-5p and miR503HG may directly interact with each other. Methylation specific PCR (MSP) showed that overexpression of miR503HG led to increased methylation level of miR-31-5p gene. Transwell assay showed that overexpression of miR-31-5p resulted in increased invasion and migration rates of OC cells. Overexpression of MiR503HG played an opposite role and attenuated the effects of overexpressing miR-31-5p. Therefore, miR503HG may promote the methylation of miR-31-5p and serve as its sponge to inhibit OC cell invasion and migration.https://doi.org/10.1186/s13048-019-0599-9Ovarian cancermiR503HGmiR-31-5pPrognosis
collection DOAJ
language English
format Article
sources DOAJ
author Ding Zhu
Xueshuang Huang
Fang Liang
Lijing Zhao
spellingShingle Ding Zhu
Xueshuang Huang
Fang Liang
Lijing Zhao
LncRNA miR503HG interacts with miR-31-5p through multiple ways to regulate cancer cell invasion and migration in ovarian cancer
Journal of Ovarian Research
Ovarian cancer
miR503HG
miR-31-5p
Prognosis
author_facet Ding Zhu
Xueshuang Huang
Fang Liang
Lijing Zhao
author_sort Ding Zhu
title LncRNA miR503HG interacts with miR-31-5p through multiple ways to regulate cancer cell invasion and migration in ovarian cancer
title_short LncRNA miR503HG interacts with miR-31-5p through multiple ways to regulate cancer cell invasion and migration in ovarian cancer
title_full LncRNA miR503HG interacts with miR-31-5p through multiple ways to regulate cancer cell invasion and migration in ovarian cancer
title_fullStr LncRNA miR503HG interacts with miR-31-5p through multiple ways to regulate cancer cell invasion and migration in ovarian cancer
title_full_unstemmed LncRNA miR503HG interacts with miR-31-5p through multiple ways to regulate cancer cell invasion and migration in ovarian cancer
title_sort lncrna mir503hg interacts with mir-31-5p through multiple ways to regulate cancer cell invasion and migration in ovarian cancer
publisher BMC
series Journal of Ovarian Research
issn 1757-2215
publishDate 2020-01-01
description Abstract The role of lncRNA miR503HG has been investigated in several types of cancer, but its functions in ovarian cancer (OC) is unclear. Analysis of TCGA dataset revealed a 50-fold lower expression level of miR503HG in OC tissues than that in non-tumor tissues, indicating the involvement of miR503HG in OC. Results in this study showed that miR503HG was downregulated in OC and predicted poor survival. Expression of miR503HG negatively correlated with the expression of miR-31-5p across OC and non-tumor tissues. RNA-RNA interaction analysis revealed that miR503HG can interact with miR-31-5p. Dual-luciferase assay showed that miR-31-5p and miR503HG may directly interact with each other. Methylation specific PCR (MSP) showed that overexpression of miR503HG led to increased methylation level of miR-31-5p gene. Transwell assay showed that overexpression of miR-31-5p resulted in increased invasion and migration rates of OC cells. Overexpression of MiR503HG played an opposite role and attenuated the effects of overexpressing miR-31-5p. Therefore, miR503HG may promote the methylation of miR-31-5p and serve as its sponge to inhibit OC cell invasion and migration.
topic Ovarian cancer
miR503HG
miR-31-5p
Prognosis
url https://doi.org/10.1186/s13048-019-0599-9
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AT xueshuanghuang lncrnamir503hginteractswithmir315pthroughmultiplewaystoregulatecancercellinvasionandmigrationinovariancancer
AT fangliang lncrnamir503hginteractswithmir315pthroughmultiplewaystoregulatecancercellinvasionandmigrationinovariancancer
AT lijingzhao lncrnamir503hginteractswithmir315pthroughmultiplewaystoregulatecancercellinvasionandmigrationinovariancancer
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