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miR-613 suppresses migration and invasion in esophageal squamous cell carcinoma via the targeting of G6PD

Esophageal squamous cell carcinoma (ESCC) is a common cancer in China and has a high mortality rate. MicroRNAs (miRs) are a family of post-transcriptional regulators, which negatively regulate target gene expression. miR-613 has been revealed to be a diagnostic and prognostic biomarker in ESCC. Howe...

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Detalles Bibliográficos
Autores principales: Su, Xiangyu, Gao, Chanchan, Feng, Xiaoyao, Jiang, Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7086187/
https://www.ncbi.nlm.nih.gov/pubmed/32256796
http://dx.doi.org/10.3892/etm.2020.8540
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author Su, Xiangyu
Gao, Chanchan
Feng, Xiaoyao
Jiang, Ming
author_facet Su, Xiangyu
Gao, Chanchan
Feng, Xiaoyao
Jiang, Ming
author_sort Su, Xiangyu
collection PubMed
description Esophageal squamous cell carcinoma (ESCC) is a common cancer in China and has a high mortality rate. MicroRNAs (miRs) are a family of post-transcriptional regulators, which negatively regulate target gene expression. miR-613 has been revealed to be a diagnostic and prognostic biomarker in ESCC. However, the role of miR-613 in ESCC remains unclear. In the present study, miR-613 expression was identified to be reduced in tumor tissues in comparison with corresponding adjacent normal tissues. TargetScan and a dual-luciferase reporter assay verified glucose-6-phosphate dehydrogenase (G6PD) as a direct target of miR-613. In contrast with miR-613, G6PD expression was increased in tumor tissues compared with matched healthy tissues. Furthermore, overexpression of miR-613 inhibited cell migration and invasion of Eca109 cells compared with controls, while G6PD overexpression reversed the inhibition induced by miR-613, as determined by wound healing and Transwell assays. In addition, miR-613 overexpression decreased the mRNA and protein expression of G6PD, matrix metalloproteinase (MMP)2 and MMP9, and reduced the phosphorylation of signal transducer and activator of transcription 3 (STAT3) compared with controls, while G6PD reversed the effects of miR-613. However, miR-613 and G6PD did not affect the expression of STAT3. In conclusion, the aforementioned results suggest that miR-613 targets G6PD to suppress ESCC cell migration and invasion through reduced MMP2 and MMP9 expression and inactivation of the STAT3 signaling pathway. Thus, the present study may provide a new molecular foundation for treatment of ESCC.
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spelling pubmed-70861872020-04-02 miR-613 suppresses migration and invasion in esophageal squamous cell carcinoma via the targeting of G6PD Su, Xiangyu Gao, Chanchan Feng, Xiaoyao Jiang, Ming Exp Ther Med Articles Esophageal squamous cell carcinoma (ESCC) is a common cancer in China and has a high mortality rate. MicroRNAs (miRs) are a family of post-transcriptional regulators, which negatively regulate target gene expression. miR-613 has been revealed to be a diagnostic and prognostic biomarker in ESCC. However, the role of miR-613 in ESCC remains unclear. In the present study, miR-613 expression was identified to be reduced in tumor tissues in comparison with corresponding adjacent normal tissues. TargetScan and a dual-luciferase reporter assay verified glucose-6-phosphate dehydrogenase (G6PD) as a direct target of miR-613. In contrast with miR-613, G6PD expression was increased in tumor tissues compared with matched healthy tissues. Furthermore, overexpression of miR-613 inhibited cell migration and invasion of Eca109 cells compared with controls, while G6PD overexpression reversed the inhibition induced by miR-613, as determined by wound healing and Transwell assays. In addition, miR-613 overexpression decreased the mRNA and protein expression of G6PD, matrix metalloproteinase (MMP)2 and MMP9, and reduced the phosphorylation of signal transducer and activator of transcription 3 (STAT3) compared with controls, while G6PD reversed the effects of miR-613. However, miR-613 and G6PD did not affect the expression of STAT3. In conclusion, the aforementioned results suggest that miR-613 targets G6PD to suppress ESCC cell migration and invasion through reduced MMP2 and MMP9 expression and inactivation of the STAT3 signaling pathway. Thus, the present study may provide a new molecular foundation for treatment of ESCC. D.A. Spandidos 2020-04 2020-02-21 /pmc/articles/PMC7086187/ /pubmed/32256796 http://dx.doi.org/10.3892/etm.2020.8540 Text en Copyright: © Su 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
Su, Xiangyu
Gao, Chanchan
Feng, Xiaoyao
Jiang, Ming
miR-613 suppresses migration and invasion in esophageal squamous cell carcinoma via the targeting of G6PD
title miR-613 suppresses migration and invasion in esophageal squamous cell carcinoma via the targeting of G6PD
title_full miR-613 suppresses migration and invasion in esophageal squamous cell carcinoma via the targeting of G6PD
title_fullStr miR-613 suppresses migration and invasion in esophageal squamous cell carcinoma via the targeting of G6PD
title_full_unstemmed miR-613 suppresses migration and invasion in esophageal squamous cell carcinoma via the targeting of G6PD
title_short miR-613 suppresses migration and invasion in esophageal squamous cell carcinoma via the targeting of G6PD
title_sort mir-613 suppresses migration and invasion in esophageal squamous cell carcinoma via the targeting of g6pd
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7086187/
https://www.ncbi.nlm.nih.gov/pubmed/32256796
http://dx.doi.org/10.3892/etm.2020.8540
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