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LncRNA WWOX-AS1 inhibits the proliferation, migration and invasion of osteosarcoma cells

Recently, numerous long non-coding (lnc)RNAs have been revealed as serving important roles in human gene regulation. Previous studies have suggested that aberrant expression of lncRNAs is associated with cancer progression and metastasis. Previous studies have also demonstrated that decreased expres...

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Autores principales: Qu, Gang, Ma, Zhiqiang, Tong, Wenxian, Yang, Jiahui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6059707/
https://www.ncbi.nlm.nih.gov/pubmed/29845204
http://dx.doi.org/10.3892/mmr.2018.9058
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author Qu, Gang
Ma, Zhiqiang
Tong, Wenxian
Yang, Jiahui
author_facet Qu, Gang
Ma, Zhiqiang
Tong, Wenxian
Yang, Jiahui
author_sort Qu, Gang
collection PubMed
description Recently, numerous long non-coding (lnc)RNAs have been revealed as serving important roles in human gene regulation. Previous studies have suggested that aberrant expression of lncRNAs is associated with cancer progression and metastasis. Previous studies have also demonstrated that decreased expression of WW domain-containing oxidoreductase (WWOX) is associated with poor prognosis in numerous cancer types. However, the effect of WWOX antisense RNA 1 (WWOX-AS1) in the development of cancer remains unknown. The aim of the present study was to investigate the role of WWOX-AS1 in osteosarcoma. The expression levels of WWOX-AS1 in human osteosarcoma cell lines and a normal osteoblastic cell line were investigated using reverse transcription-quantitative polymerase chain reaction (RT-qPCR). The results revealed that WWOX-AS1 expression was downregulated in osteosarcoma tissues. Furthermore, the association between WWOX-AS1 and the prognosis of patients with osteosarcoma was investigated using Kaplan-Meier and log-rank tests. The results suggested that patients exhibiting high WWOX-AS1 expression demonstrated a greater overall survival compared with patients exhibiting low WWOX-AS1 expression. In addition, overexpression and knockdown of WWOX-AS1 was performed using transfection experiments and confirmed by RT-qPCR in MG63 and SAOS2 cells, respectively. The results demonstrated that WWOX-AS1 and WWOX expression were positively correlated. Furthermore, the results of the knockdown and overexpression functional experiments suggested that WWOX-AS1 overexpression inhibited the proliferation, migration and invasion of MG63 cells, and knockdown of WWOX-AS1 enhanced the proliferation, migration and invasion of MG63 cells in SAOS2 cells. In conclusion, the results of the present study suggested that WWOX-AS1 may represent a potential biomarker and therapeutic target for the treatment of osteosarcoma.
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spelling pubmed-60597072018-07-26 LncRNA WWOX-AS1 inhibits the proliferation, migration and invasion of osteosarcoma cells Qu, Gang Ma, Zhiqiang Tong, Wenxian Yang, Jiahui Mol Med Rep Articles Recently, numerous long non-coding (lnc)RNAs have been revealed as serving important roles in human gene regulation. Previous studies have suggested that aberrant expression of lncRNAs is associated with cancer progression and metastasis. Previous studies have also demonstrated that decreased expression of WW domain-containing oxidoreductase (WWOX) is associated with poor prognosis in numerous cancer types. However, the effect of WWOX antisense RNA 1 (WWOX-AS1) in the development of cancer remains unknown. The aim of the present study was to investigate the role of WWOX-AS1 in osteosarcoma. The expression levels of WWOX-AS1 in human osteosarcoma cell lines and a normal osteoblastic cell line were investigated using reverse transcription-quantitative polymerase chain reaction (RT-qPCR). The results revealed that WWOX-AS1 expression was downregulated in osteosarcoma tissues. Furthermore, the association between WWOX-AS1 and the prognosis of patients with osteosarcoma was investigated using Kaplan-Meier and log-rank tests. The results suggested that patients exhibiting high WWOX-AS1 expression demonstrated a greater overall survival compared with patients exhibiting low WWOX-AS1 expression. In addition, overexpression and knockdown of WWOX-AS1 was performed using transfection experiments and confirmed by RT-qPCR in MG63 and SAOS2 cells, respectively. The results demonstrated that WWOX-AS1 and WWOX expression were positively correlated. Furthermore, the results of the knockdown and overexpression functional experiments suggested that WWOX-AS1 overexpression inhibited the proliferation, migration and invasion of MG63 cells, and knockdown of WWOX-AS1 enhanced the proliferation, migration and invasion of MG63 cells in SAOS2 cells. In conclusion, the results of the present study suggested that WWOX-AS1 may represent a potential biomarker and therapeutic target for the treatment of osteosarcoma. D.A. Spandidos 2018-07 2018-05-23 /pmc/articles/PMC6059707/ /pubmed/29845204 http://dx.doi.org/10.3892/mmr.2018.9058 Text en Copyright: © Qu et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Qu, Gang
Ma, Zhiqiang
Tong, Wenxian
Yang, Jiahui
LncRNA WWOX-AS1 inhibits the proliferation, migration and invasion of osteosarcoma cells
title LncRNA WWOX-AS1 inhibits the proliferation, migration and invasion of osteosarcoma cells
title_full LncRNA WWOX-AS1 inhibits the proliferation, migration and invasion of osteosarcoma cells
title_fullStr LncRNA WWOX-AS1 inhibits the proliferation, migration and invasion of osteosarcoma cells
title_full_unstemmed LncRNA WWOX-AS1 inhibits the proliferation, migration and invasion of osteosarcoma cells
title_short LncRNA WWOX-AS1 inhibits the proliferation, migration and invasion of osteosarcoma cells
title_sort lncrna wwox-as1 inhibits the proliferation, migration and invasion of osteosarcoma cells
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6059707/
https://www.ncbi.nlm.nih.gov/pubmed/29845204
http://dx.doi.org/10.3892/mmr.2018.9058
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