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Circ_0061140 stimulates the malignant development of prostate cancer by targeting miR-1193

BACKGROUND: This study sought to explore the expression pattern in prostate cancer (PCa) tissues, as well as the regulatory effects of circ_0061140 on the proliferative potential of PCa cells. METHODS: A quantitative real-time polymerase chain reaction (qRT-PCR) analysis was undertaken to detect cir...

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Detalles Bibliográficos
Autores principales: Wang, Kai, Fan, Yi, Sun, Ji, Zhao, Liwei, Yu, Yufu, Li, Gonghui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8185672/
https://www.ncbi.nlm.nih.gov/pubmed/34159074
http://dx.doi.org/10.21037/tau-20-1477
Descripción
Sumario:BACKGROUND: This study sought to explore the expression pattern in prostate cancer (PCa) tissues, as well as the regulatory effects of circ_0061140 on the proliferative potential of PCa cells. METHODS: A quantitative real-time polymerase chain reaction (qRT-PCR) analysis was undertaken to detect circ_0061140 levels in 43 paired PCa tissues and adjacent normal tissues. After the knockdown of circ_0061140, changes in the proliferative potential of PCa cells and tumor growth in nude mice with PCa were detected. Finally, the relationship of circ_0061140 and miR-1193 in the development of PCa was assessed. RESULTS: The results showed that circ_0061140 was upregulated in PCa tissues. PCa patients with higher Gleason score or larger sized tumors expressed higher levels of circ_0061140. Additionally, the knockdown of circ_0061140 inhibited the proliferative potential of PCa cells. MiR-1193 was the target gene binding circ_0061140, and its level was negatively regulated by circ_0061140. Finally, rescue experiments showed that miR-1193 was regulated by circ_0061140 in the development of PCa. CONCLUSIONS: Circ_0061140 is upregulated in PCa tissues, and is closely linked to Gleason score and tumor size in PCa. Additionally, it causes PCa cells to proliferate by negatively regulating miR-1193.