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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2021
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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 |
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author | Wang, Kai Fan, Yi Sun, Ji Zhao, Liwei Yu, Yufu Li, Gonghui |
author_facet | Wang, Kai Fan, Yi Sun, Ji Zhao, Liwei Yu, Yufu Li, Gonghui |
author_sort | Wang, Kai |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-8185672 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-81856722021-06-21 Circ_0061140 stimulates the malignant development of prostate cancer by targeting miR-1193 Wang, Kai Fan, Yi Sun, Ji Zhao, Liwei Yu, Yufu Li, Gonghui Transl Androl Urol Original Article 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. AME Publishing Company 2021-05 /pmc/articles/PMC8185672/ /pubmed/34159074 http://dx.doi.org/10.21037/tau-20-1477 Text en 2021 Translational Andrology and Urology. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Original Article Wang, Kai Fan, Yi Sun, Ji Zhao, Liwei Yu, Yufu Li, Gonghui Circ_0061140 stimulates the malignant development of prostate cancer by targeting miR-1193 |
title | Circ_0061140 stimulates the malignant development of prostate cancer by targeting miR-1193 |
title_full | Circ_0061140 stimulates the malignant development of prostate cancer by targeting miR-1193 |
title_fullStr | Circ_0061140 stimulates the malignant development of prostate cancer by targeting miR-1193 |
title_full_unstemmed | Circ_0061140 stimulates the malignant development of prostate cancer by targeting miR-1193 |
title_short | Circ_0061140 stimulates the malignant development of prostate cancer by targeting miR-1193 |
title_sort | circ_0061140 stimulates the malignant development of prostate cancer by targeting mir-1193 |
topic | Original Article |
url | 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 |
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