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Circular RNA circABCC4 as the ceRNA of miR‐1182 facilitates prostate cancer progression by promoting FOXP4 expression
- Source :
- Journal of Cellular and Molecular Medicine
- Publication Year :
- 2019
- Publisher :
- Wiley, 2019.
-
Abstract
- In recent years, circular RNAs (circRNAs) have been identified to be essential regulators of various human cancers. However, knowledge of the functions of circRNAs in prostate cancer remains very limited. The correlation between circABCC4 and human cancer is largely unknown. This study aims to investigate the biological functions of circABCC4 in prostate cancer progression and illustrate the underlying mechanism. We found that circABCC4 was remarkably up‐regulated in prostate cancer tissues and cell lines and promoted FOXP4 expression by sponging miR‐1182 in prostate cancer cells. CircABCC4 knockdown markedly suppressed prostate cancer cell proliferation, cell‐cycle progression, migration and invasion in vitro. Furthermore, silencing of the circRNA also delayed tumor growth in vivo. Taken together, our findings indicated that circABCC4 facilitates the malignant behaviour of prostate cancer by promoting FOXP4 expression through sponging of miR‐1182. The circABCC4–miR‐1182‐FOXP4 regulatory loop may be a promising therapeutic target for prostate cancer intervention.
- Subjects :
- Male
0301 basic medicine
proliferation
FOXP4
Biology
migration
Mice
03 medical and health sciences
Prostate cancer
0302 clinical medicine
Cell Movement
In vivo
Circular RNA
Cell Line, Tumor
medicine
Animals
Humans
Gene silencing
circABCC4
Aged
Cell Proliferation
Gene knockdown
Mechanism (biology)
Competing endogenous RNA
Prostatic Neoplasms
Forkhead Transcription Factors
RNA, Circular
Original Articles
Cell Biology
Middle Aged
prostate cancer
medicine.disease
Gene Expression Regulation, Neoplastic
MicroRNAs
030104 developmental biology
Cell culture
030220 oncology & carcinogenesis
Disease Progression
Cancer research
Heterografts
Molecular Medicine
Original Article
Subjects
Details
- ISSN :
- 15824934 and 15821838
- Volume :
- 23
- Database :
- OpenAIRE
- Journal :
- Journal of Cellular and Molecular Medicine
- Accession number :
- edsair.doi.dedup.....674b21f6ad8c57d29ec19e9939120c51