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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.
Afiliação
  • Jia Q; Department of Radiology, East Hospital, Xiamen University, Fuzhou, China.
  • Ye L; Department of Radiology, Zhengxing Hospital, Zhangzhou, China.
  • Xu S; Department of Nursing, Zhangzhou Health Vocational College, Zhangzhou, China.
  • Xiao H; Department of Radiology, East Hospital, Xiamen University, Fuzhou, China.
  • Xu S; Department of Radiology, East Hospital, Xiamen University, Fuzhou, China.
  • Shi Z; Department of Radiology, Zhengxing Hospital, Zhangzhou, China.
  • Li J; Department of Radiology, Zhengxing Hospital, Zhangzhou, China.
  • Chen Z; Department of Radiology, Zhengxing Hospital, Zhangzhou, China.
Thorac Cancer ; 11(3): 619-630, 2020 03.
Article em En | MEDLINE | ID: mdl-31962380
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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Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 6_ODS3_enfermedades_notrasmisibles Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Biomarcadores Tumorais / Regulação Neoplásica da Expressão Gênica / Proteínas de Homeodomínio / MicroRNAs / RNA Circular / Proteínas do Tecido Nervoso Tipo de estudo: Observational_studies / Prognostic_studies Limite: Animals / Female / Humans Idioma: En Revista: Thorac Cancer Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 6_ODS3_enfermedades_notrasmisibles Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Biomarcadores Tumorais / Regulação Neoplásica da Expressão Gênica / Proteínas de Homeodomínio / MicroRNAs / RNA Circular / Proteínas do Tecido Nervoso Tipo de estudo: Observational_studies / Prognostic_studies Limite: Animals / Female / Humans Idioma: En Revista: Thorac Cancer Ano de publicação: 2020 Tipo de documento: Article