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The Regulatory Role of circRNA_101308 in Cervical Cancer and the Prediction of Its Mechanism

PURPOSE: Accumulating evidence indicates that circular RNAs (circRNAs) are closely involved in canceration and cancer progression. However, the role of circRNAs in cervical cancer (CC) is largely unknown. Here, we characterized the role of circRNA_101308 in CC. MATERIALS AND METHODS: The expression...

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Autores principales: Jiao, Jun, Jiao, Xinlin, Liu, Qingqing, Qu, Wenjie, Ma, Daoxin, Zhang, Youzhong, Cui, Baoxia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7319513/
https://www.ncbi.nlm.nih.gov/pubmed/32606970
http://dx.doi.org/10.2147/CMAR.S242615
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author Jiao, Jun
Jiao, Xinlin
Liu, Qingqing
Qu, Wenjie
Ma, Daoxin
Zhang, Youzhong
Cui, Baoxia
author_facet Jiao, Jun
Jiao, Xinlin
Liu, Qingqing
Qu, Wenjie
Ma, Daoxin
Zhang, Youzhong
Cui, Baoxia
author_sort Jiao, Jun
collection PubMed
description PURPOSE: Accumulating evidence indicates that circular RNAs (circRNAs) are closely involved in canceration and cancer progression. However, the role of circRNAs in cervical cancer (CC) is largely unknown. Here, we characterized the role of circRNA_101308 in CC. MATERIALS AND METHODS: The expression of circRNA_101308 in CC tissues was measured by quantitative reverse transcription-polymerase chain reaction (qRT-PCR). Then, circRNA_101308 was overexpressed in CC cells to detect its function by proliferation and apoptosis assays, Transwell assays and animal experiments. The potential mechanism of circRNA_101308 in CC was explored by RNA pull-down, Gene Ontology (GO) and pathway analyses. RESULTS: CircRNA_101308 was significantly downregulated in CC tissues. The level of circRNA_101308 was much lower in CC patients with lymph node metastasis or deep myometrial invasion compared to those patients without lymph node metastasis and superficial myometrial invasion. CircRNA_101308 overexpression inhibited CC cell proliferation, invasion and migration. MiR-26a-5p, miR-196a-5p, miR-196b-5p, miR-335-3p, and miR-1307-3p were found to be sponged by circRNA_101308 in CC cells. Further, GO and pathway analyses predicted the potential functional processes and pathways of circRNA_101308 in CC. CONCLUSION: CircRNA_101308 is downregulated and acts as a tumor suppressor in CC. CircRNA_101308 can participate in many different processes by sponging different miRNAs in CC cells. This exploration of circRNA_101308 provides new directions for research on cancer development and the clinical treatment of CC.
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spelling pubmed-73195132020-06-29 The Regulatory Role of circRNA_101308 in Cervical Cancer and the Prediction of Its Mechanism Jiao, Jun Jiao, Xinlin Liu, Qingqing Qu, Wenjie Ma, Daoxin Zhang, Youzhong Cui, Baoxia Cancer Manag Res Original Research PURPOSE: Accumulating evidence indicates that circular RNAs (circRNAs) are closely involved in canceration and cancer progression. However, the role of circRNAs in cervical cancer (CC) is largely unknown. Here, we characterized the role of circRNA_101308 in CC. MATERIALS AND METHODS: The expression of circRNA_101308 in CC tissues was measured by quantitative reverse transcription-polymerase chain reaction (qRT-PCR). Then, circRNA_101308 was overexpressed in CC cells to detect its function by proliferation and apoptosis assays, Transwell assays and animal experiments. The potential mechanism of circRNA_101308 in CC was explored by RNA pull-down, Gene Ontology (GO) and pathway analyses. RESULTS: CircRNA_101308 was significantly downregulated in CC tissues. The level of circRNA_101308 was much lower in CC patients with lymph node metastasis or deep myometrial invasion compared to those patients without lymph node metastasis and superficial myometrial invasion. CircRNA_101308 overexpression inhibited CC cell proliferation, invasion and migration. MiR-26a-5p, miR-196a-5p, miR-196b-5p, miR-335-3p, and miR-1307-3p were found to be sponged by circRNA_101308 in CC cells. Further, GO and pathway analyses predicted the potential functional processes and pathways of circRNA_101308 in CC. CONCLUSION: CircRNA_101308 is downregulated and acts as a tumor suppressor in CC. CircRNA_101308 can participate in many different processes by sponging different miRNAs in CC cells. This exploration of circRNA_101308 provides new directions for research on cancer development and the clinical treatment of CC. Dove 2020-06-22 /pmc/articles/PMC7319513/ /pubmed/32606970 http://dx.doi.org/10.2147/CMAR.S242615 Text en © 2020 Jiao et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Jiao, Jun
Jiao, Xinlin
Liu, Qingqing
Qu, Wenjie
Ma, Daoxin
Zhang, Youzhong
Cui, Baoxia
The Regulatory Role of circRNA_101308 in Cervical Cancer and the Prediction of Its Mechanism
title The Regulatory Role of circRNA_101308 in Cervical Cancer and the Prediction of Its Mechanism
title_full The Regulatory Role of circRNA_101308 in Cervical Cancer and the Prediction of Its Mechanism
title_fullStr The Regulatory Role of circRNA_101308 in Cervical Cancer and the Prediction of Its Mechanism
title_full_unstemmed The Regulatory Role of circRNA_101308 in Cervical Cancer and the Prediction of Its Mechanism
title_short The Regulatory Role of circRNA_101308 in Cervical Cancer and the Prediction of Its Mechanism
title_sort regulatory role of circrna_101308 in cervical cancer and the prediction of its mechanism
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7319513/
https://www.ncbi.nlm.nih.gov/pubmed/32606970
http://dx.doi.org/10.2147/CMAR.S242615
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