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Circular RNA 0007255 regulates the progression of breast cancer through miR‐335‐5p/SIX2 axis

BACKGROUND: Breast cancer (BC) is a common cancer in women worldwide. Emerging evidence has indicated that circular RNA hsa‐circ_0007255 (circ_0007255) is a prognostic mediator in BC progression. However, the functional role of circ_0007255 needs to be determined. METHODS: The expression of circ_000...

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Autores principales: Jia, Qianxin, Ye, Lanlan, Xu, Shangwen, Xiao, Hui, Xu, Siding, Shi, Zhaoyin, Li, Jinsheng, Chen, Ziqian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons Australia, Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7049509/
https://www.ncbi.nlm.nih.gov/pubmed/31962380
http://dx.doi.org/10.1111/1759-7714.13306
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author Jia, Qianxin
Ye, Lanlan
Xu, Shangwen
Xiao, Hui
Xu, Siding
Shi, Zhaoyin
Li, Jinsheng
Chen, Ziqian
author_facet Jia, Qianxin
Ye, Lanlan
Xu, Shangwen
Xiao, Hui
Xu, Siding
Shi, Zhaoyin
Li, Jinsheng
Chen, Ziqian
author_sort Jia, Qianxin
collection PubMed
description BACKGROUND: Breast cancer (BC) is a common cancer in women worldwide. Emerging evidence has indicated that circular RNA hsa‐circ_0007255 (circ_0007255) is a prognostic mediator in BC progression. However, the functional role of circ_0007255 needs to be determined. METHODS: The expression of circ_0007255, microRNA (miR)‐335‐5p, and SIX Homeobox 2 (SIX2) was evaluated using quantitative real‐time polymerase chain reaction (qRT‐PCR) or western blot assay. Actinomycin D and RNase R treatment was performed to analyze the stability of circ_0007255. Additionally, Seahorse extracellular flux, colony formation and transwell analyses were carried out to detect oxygen consumption ratio (OCR), colony formation and cell mobility, respectively. The interaction between miR‐335‐5p and circ_0007255 or SIX2 was confirmed via dual‐luciferase reporter assay. A xenograft tumor model was established to explore the role of circ_0007255 in vivo. RESULTS: Circ_0007255 and SIX2 were overexpressed, but miR‐335‐5p was diminished in BC tissues and cells. Circ_0007255 absence inhibited oxygen consumption, colony formation, cell migration and invasion, and these effects were particularly abrogated via miR‐335‐5p upregulation in BC cells. Moreover, SIX2 deficiency eliminated the promotion effects of miR‐335‐5p inhibitor on oxygen consumption, colony formation, and cell mobility in BC cells. Importantly, circ_0007255 inhibited tumor growth in vivo. Mechanically, circ_0007255 was a sponge of miR‐335‐5p to regulate SIX2 expression in BC progression. CONCLUSION: Circ_0007255 functioned as a novel oncogene in the progression of BC by regulating miR‐335‐5p/SIX2 axis, and might be a promising biomarker for BC treatment. KEY POINTS: Significant findings of the study: Levels of circ_0007255 and SIX2 were upregulated, but miR‐335‐5p was diminished in BC tissues and cells. Circ_0007255 was an oncogene in BC development and exerted its function via miR‐335‐5p/SIX2 axis in BC. Tumor growth was reduced by circ_0007255 absence. What this study adds: Circ_0007255 functioned as a novel oncogene in the progression of BC by regulating miR‐335‐5p/SIX2 axis, and might be a promising biomarker for BC treatment.
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spelling pubmed-70495092020-03-05 Circular RNA 0007255 regulates the progression of breast cancer through miR‐335‐5p/SIX2 axis Jia, Qianxin Ye, Lanlan Xu, Shangwen Xiao, Hui Xu, Siding Shi, Zhaoyin Li, Jinsheng Chen, Ziqian Thorac Cancer Original Articles BACKGROUND: Breast cancer (BC) is a common cancer in women worldwide. Emerging evidence has indicated that circular RNA hsa‐circ_0007255 (circ_0007255) is a prognostic mediator in BC progression. However, the functional role of circ_0007255 needs to be determined. METHODS: The expression of circ_0007255, microRNA (miR)‐335‐5p, and SIX Homeobox 2 (SIX2) was evaluated using quantitative real‐time polymerase chain reaction (qRT‐PCR) or western blot assay. Actinomycin D and RNase R treatment was performed to analyze the stability of circ_0007255. Additionally, Seahorse extracellular flux, colony formation and transwell analyses were carried out to detect oxygen consumption ratio (OCR), colony formation and cell mobility, respectively. The interaction between miR‐335‐5p and circ_0007255 or SIX2 was confirmed via dual‐luciferase reporter assay. A xenograft tumor model was established to explore the role of circ_0007255 in vivo. RESULTS: Circ_0007255 and SIX2 were overexpressed, but miR‐335‐5p was diminished in BC tissues and cells. Circ_0007255 absence inhibited oxygen consumption, colony formation, cell migration and invasion, and these effects were particularly abrogated via miR‐335‐5p upregulation in BC cells. Moreover, SIX2 deficiency eliminated the promotion effects of miR‐335‐5p inhibitor on oxygen consumption, colony formation, and cell mobility in BC cells. Importantly, circ_0007255 inhibited tumor growth in vivo. Mechanically, circ_0007255 was a sponge of miR‐335‐5p to regulate SIX2 expression in BC progression. CONCLUSION: Circ_0007255 functioned as a novel oncogene in the progression of BC by regulating miR‐335‐5p/SIX2 axis, and might be a promising biomarker for BC treatment. KEY POINTS: Significant findings of the study: Levels of circ_0007255 and SIX2 were upregulated, but miR‐335‐5p was diminished in BC tissues and cells. Circ_0007255 was an oncogene in BC development and exerted its function via miR‐335‐5p/SIX2 axis in BC. Tumor growth was reduced by circ_0007255 absence. What this study adds: Circ_0007255 functioned as a novel oncogene in the progression of BC by regulating miR‐335‐5p/SIX2 axis, and might be a promising biomarker for BC treatment. John Wiley & Sons Australia, Ltd 2020-01-21 2020-03 /pmc/articles/PMC7049509/ /pubmed/31962380 http://dx.doi.org/10.1111/1759-7714.13306 Text en © 2020 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, 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 Original Articles
Jia, Qianxin
Ye, Lanlan
Xu, Shangwen
Xiao, Hui
Xu, Siding
Shi, Zhaoyin
Li, Jinsheng
Chen, Ziqian
Circular RNA 0007255 regulates the progression of breast cancer through miR‐335‐5p/SIX2 axis
title Circular RNA 0007255 regulates the progression of breast cancer through miR‐335‐5p/SIX2 axis
title_full Circular RNA 0007255 regulates the progression of breast cancer through miR‐335‐5p/SIX2 axis
title_fullStr Circular RNA 0007255 regulates the progression of breast cancer through miR‐335‐5p/SIX2 axis
title_full_unstemmed Circular RNA 0007255 regulates the progression of breast cancer through miR‐335‐5p/SIX2 axis
title_short Circular RNA 0007255 regulates the progression of breast cancer through miR‐335‐5p/SIX2 axis
title_sort circular rna 0007255 regulates the progression of breast cancer through mir‐335‐5p/six2 axis
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7049509/
https://www.ncbi.nlm.nih.gov/pubmed/31962380
http://dx.doi.org/10.1111/1759-7714.13306
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