MicroRNA-1246 Promotes Melanoma Progression Through Targeting FOXA2

Yanhua Yu,1 Fang Yu,1 Pijiang Sun2 1Department of Dermatology, Weihai Central Hospital Affiliated to Qingdao University, Weihai 264400, People’s Republic of China; 2Department of Hepatobiliary and Abdominal Hernias Surgery, Weihai Central Hospital Affiliated to Qingdao University, Weihai 2...

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Main Authors: Yu Y, Yu F, Sun P
Format: Article
Language:English
Published: Dove Medical Press 2020-02-01
Series:OncoTargets and Therapy
Subjects:
Online Access:https://www.dovepress.com/microrna-1246-promotes-melanoma-progression-through-targeting-foxa2-peer-reviewed-article-OTT
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spelling doaj-89fb67bab4d24462b4c762ac221645152020-11-25T01:19:52ZengDove Medical PressOncoTargets and Therapy1178-69302020-02-01Volume 131245125351708MicroRNA-1246 Promotes Melanoma Progression Through Targeting FOXA2Yu YYu FSun PYanhua Yu,1 Fang Yu,1 Pijiang Sun2 1Department of Dermatology, Weihai Central Hospital Affiliated to Qingdao University, Weihai 264400, People’s Republic of China; 2Department of Hepatobiliary and Abdominal Hernias Surgery, Weihai Central Hospital Affiliated to Qingdao University, Weihai 264400, People’s Republic of ChinaCorrespondence: Pijiang SunDepartment of Hepatobiliary and Abdominal Hernias Surgery, Weihai Central Hospital Affiliated to Qingdao University, No. 3 Mishandong Road, Wendeng District, Weihai 264400, Shandong, People’s Republic of ChinaTel +86 152 6441 0981Email beciham@163.comIntroduction: Recently, the incidence of melanoma has been rising and there is a lack of effective targeted therapies. The regulatory mechanisms of microRNA-1246 (miR-1246) have been found in many cancers, except melanoma. This study focused on the regulatory mechanism of miR-1246 in melanoma development.Methods: The expression of miR-1246 was assessed using quantitative real-time polymerase chain reaction (RT-qPCR). Cell viability and metastasis were detected by Transwell and MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide) assays. The protein expression of epithelial mesenchymal transition (EMT) makers was assessed by Western blot analysis. The target gene of miR-1246 was detected using luciferase reporter assay.Results: MiR-1246 expression was increased in melanoma tissues and cells. In addition, upregulation of miR-1246 promoted cell viability and metastasis in melanoma. Forkhead box protein A2 (FOXA2) was confirmed to be a direct target of miR-1246. And FOXA2 expression was decreased in melanoma and was suppressed by miR-1246. Importantly, upregulation of FOXA2 restored the carcinogenesis of miR-1246 in melanoma.Conclusion: MiR-1246 promoted cell viability and metastasis in melanoma by inhibiting FOXA2 expression.Keywords: miR-1246, melanoma, cell viability, cell metastasis, FOXA2https://www.dovepress.com/microrna-1246-promotes-melanoma-progression-through-targeting-foxa2-peer-reviewed-article-OTTmir-1246melanomacell viabilitycell metastasisfoxa2
collection DOAJ
language English
format Article
sources DOAJ
author Yu Y
Yu F
Sun P
spellingShingle Yu Y
Yu F
Sun P
MicroRNA-1246 Promotes Melanoma Progression Through Targeting FOXA2
OncoTargets and Therapy
mir-1246
melanoma
cell viability
cell metastasis
foxa2
author_facet Yu Y
Yu F
Sun P
author_sort Yu Y
title MicroRNA-1246 Promotes Melanoma Progression Through Targeting FOXA2
title_short MicroRNA-1246 Promotes Melanoma Progression Through Targeting FOXA2
title_full MicroRNA-1246 Promotes Melanoma Progression Through Targeting FOXA2
title_fullStr MicroRNA-1246 Promotes Melanoma Progression Through Targeting FOXA2
title_full_unstemmed MicroRNA-1246 Promotes Melanoma Progression Through Targeting FOXA2
title_sort microrna-1246 promotes melanoma progression through targeting foxa2
publisher Dove Medical Press
series OncoTargets and Therapy
issn 1178-6930
publishDate 2020-02-01
description Yanhua Yu,1 Fang Yu,1 Pijiang Sun2 1Department of Dermatology, Weihai Central Hospital Affiliated to Qingdao University, Weihai 264400, People’s Republic of China; 2Department of Hepatobiliary and Abdominal Hernias Surgery, Weihai Central Hospital Affiliated to Qingdao University, Weihai 264400, People’s Republic of ChinaCorrespondence: Pijiang SunDepartment of Hepatobiliary and Abdominal Hernias Surgery, Weihai Central Hospital Affiliated to Qingdao University, No. 3 Mishandong Road, Wendeng District, Weihai 264400, Shandong, People’s Republic of ChinaTel +86 152 6441 0981Email beciham@163.comIntroduction: Recently, the incidence of melanoma has been rising and there is a lack of effective targeted therapies. The regulatory mechanisms of microRNA-1246 (miR-1246) have been found in many cancers, except melanoma. This study focused on the regulatory mechanism of miR-1246 in melanoma development.Methods: The expression of miR-1246 was assessed using quantitative real-time polymerase chain reaction (RT-qPCR). Cell viability and metastasis were detected by Transwell and MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide) assays. The protein expression of epithelial mesenchymal transition (EMT) makers was assessed by Western blot analysis. The target gene of miR-1246 was detected using luciferase reporter assay.Results: MiR-1246 expression was increased in melanoma tissues and cells. In addition, upregulation of miR-1246 promoted cell viability and metastasis in melanoma. Forkhead box protein A2 (FOXA2) was confirmed to be a direct target of miR-1246. And FOXA2 expression was decreased in melanoma and was suppressed by miR-1246. Importantly, upregulation of FOXA2 restored the carcinogenesis of miR-1246 in melanoma.Conclusion: MiR-1246 promoted cell viability and metastasis in melanoma by inhibiting FOXA2 expression.Keywords: miR-1246, melanoma, cell viability, cell metastasis, FOXA2
topic mir-1246
melanoma
cell viability
cell metastasis
foxa2
url https://www.dovepress.com/microrna-1246-promotes-melanoma-progression-through-targeting-foxa2-peer-reviewed-article-OTT
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