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CircNEIL3 promotes cervical cancer cell proliferation by adsorbing miR-137 and upregulating KLF12
BACKGROUND: CircRNAs play crucial roles in multiple tumours. However, the functions of most circRNAs in cervical cancer remain unclear. METHODS: This study collected GSE113696 data from the GEO database to search for differentially expressed circRNAs in cervical cancer. Quantitative reverse transcri...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7792354/ https://www.ncbi.nlm.nih.gov/pubmed/33413360 http://dx.doi.org/10.1186/s12935-020-01736-4 |
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author | Chen, Yuan Geng, Yiting Huang, Junchao Xi, Dan Xu, Guoping Gu, Wendong Shao, Yingjie |
author_facet | Chen, Yuan Geng, Yiting Huang, Junchao Xi, Dan Xu, Guoping Gu, Wendong Shao, Yingjie |
author_sort | Chen, Yuan |
collection | PubMed |
description | BACKGROUND: CircRNAs play crucial roles in multiple tumours. However, the functions of most circRNAs in cervical cancer remain unclear. METHODS: This study collected GSE113696 data from the GEO database to search for differentially expressed circRNAs in cervical cancer. Quantitative reverse transcription PCR was used to detect the expression level of circNEIL3 in cervical cancer cells and tissues. Then, functional experiments in vitro and in vivo were performed to evaluate the effects of circNEIL3 in cervical cancer. RESULTS: CircNEIL3 was highly expressed in cervical cancer. In vivo and in vitro experiments verified that circNEIL3 enhanced the proliferation capacity of cervical cancer cells. RNA immunoprecipitation, luciferase reporter assay, pull-down assay, and fluorescent in situ hybridization confirmed the interaction between circNEIL3 and miR-137 in cervical cancer. A luciferase reporter assay showed that circNEIL3 adsorbed miR-137 and upregulated KLF12 to regulate the proliferation of cervical cancer cells. CONCLUSIONS: CircNEIL3 is an oncogene in cervical cancer and might serve as a ceRNA that competitively binds to miR-137, thereby indirectly upregulating the expression of KLF12 and promoting the proliferation of cervical cancer cells. |
format | Online Article Text |
id | pubmed-7792354 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-77923542021-01-11 CircNEIL3 promotes cervical cancer cell proliferation by adsorbing miR-137 and upregulating KLF12 Chen, Yuan Geng, Yiting Huang, Junchao Xi, Dan Xu, Guoping Gu, Wendong Shao, Yingjie Cancer Cell Int Primary Research BACKGROUND: CircRNAs play crucial roles in multiple tumours. However, the functions of most circRNAs in cervical cancer remain unclear. METHODS: This study collected GSE113696 data from the GEO database to search for differentially expressed circRNAs in cervical cancer. Quantitative reverse transcription PCR was used to detect the expression level of circNEIL3 in cervical cancer cells and tissues. Then, functional experiments in vitro and in vivo were performed to evaluate the effects of circNEIL3 in cervical cancer. RESULTS: CircNEIL3 was highly expressed in cervical cancer. In vivo and in vitro experiments verified that circNEIL3 enhanced the proliferation capacity of cervical cancer cells. RNA immunoprecipitation, luciferase reporter assay, pull-down assay, and fluorescent in situ hybridization confirmed the interaction between circNEIL3 and miR-137 in cervical cancer. A luciferase reporter assay showed that circNEIL3 adsorbed miR-137 and upregulated KLF12 to regulate the proliferation of cervical cancer cells. CONCLUSIONS: CircNEIL3 is an oncogene in cervical cancer and might serve as a ceRNA that competitively binds to miR-137, thereby indirectly upregulating the expression of KLF12 and promoting the proliferation of cervical cancer cells. BioMed Central 2021-01-07 /pmc/articles/PMC7792354/ /pubmed/33413360 http://dx.doi.org/10.1186/s12935-020-01736-4 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Primary Research Chen, Yuan Geng, Yiting Huang, Junchao Xi, Dan Xu, Guoping Gu, Wendong Shao, Yingjie CircNEIL3 promotes cervical cancer cell proliferation by adsorbing miR-137 and upregulating KLF12 |
title | CircNEIL3 promotes cervical cancer cell proliferation by adsorbing miR-137 and upregulating KLF12 |
title_full | CircNEIL3 promotes cervical cancer cell proliferation by adsorbing miR-137 and upregulating KLF12 |
title_fullStr | CircNEIL3 promotes cervical cancer cell proliferation by adsorbing miR-137 and upregulating KLF12 |
title_full_unstemmed | CircNEIL3 promotes cervical cancer cell proliferation by adsorbing miR-137 and upregulating KLF12 |
title_short | CircNEIL3 promotes cervical cancer cell proliferation by adsorbing miR-137 and upregulating KLF12 |
title_sort | circneil3 promotes cervical cancer cell proliferation by adsorbing mir-137 and upregulating klf12 |
topic | Primary Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7792354/ https://www.ncbi.nlm.nih.gov/pubmed/33413360 http://dx.doi.org/10.1186/s12935-020-01736-4 |
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