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Circ-TRIO promotes TNBC progression by regulating the miR-432-5p/CCDC58 axis
Numerous studies have shown that circRNAs are aberrantly expressed in various cancers and play a significant role in tumor progression. However, the molecular mechanisms of circRNAs in triple-negative breast cancer (TNBC) remain ambiguous. By intersecting throughput data and qRT-PCR results from tis...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9458743/ https://www.ncbi.nlm.nih.gov/pubmed/36075896 http://dx.doi.org/10.1038/s41419-022-05216-7 |
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author | Wang, Zekun Li, Yaming Yang, Jingwen Liang, Yiran Wang, Xiaolong Zhang, Ning Kong, Xiaoli Chen, Bing Wang, Lijuan Zhao, Wenjing Yang, Qifeng |
author_facet | Wang, Zekun Li, Yaming Yang, Jingwen Liang, Yiran Wang, Xiaolong Zhang, Ning Kong, Xiaoli Chen, Bing Wang, Lijuan Zhao, Wenjing Yang, Qifeng |
author_sort | Wang, Zekun |
collection | PubMed |
description | Numerous studies have shown that circRNAs are aberrantly expressed in various cancers and play a significant role in tumor progression. However, the molecular mechanisms of circRNAs in triple-negative breast cancer (TNBC) remain ambiguous. By intersecting throughput data and qRT-PCR results from tissues and cell lines, circ-TRIO was identified as a potential oncogenic regulator of TNBC. Moreover, circ-TRIO expression was detected in TNBC tissues and was correlated with the recurrence and prognosis of TNBC patients. The circular characteristics of circ-TRIO were verified by RNase R and CHX assays. Functionally, the knockdown of circ-TRIO inhibited the proliferation, migration and invasion of TNBC cells, while the overexpression of circ-TRIO resulted in the opposite impacts. Mechanistically, a dual luciferase reporter assay and RNA immunoprecipitation were performed and indicated that circ-TRIO could combine with miR-432-5p to regulate the expression of coiled-coil domain containing 58 (CCDC58). In summary, our study illustrates that circ-TRIO plays an important role in the progression of TNBC by regulating the miR-432-5p/CCDC58 axis, which could broaden our insight into the underlying mechanisms and provide a novel prognostic marker of TNBC in the clinic. |
format | Online Article Text |
id | pubmed-9458743 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-94587432022-09-10 Circ-TRIO promotes TNBC progression by regulating the miR-432-5p/CCDC58 axis Wang, Zekun Li, Yaming Yang, Jingwen Liang, Yiran Wang, Xiaolong Zhang, Ning Kong, Xiaoli Chen, Bing Wang, Lijuan Zhao, Wenjing Yang, Qifeng Cell Death Dis Article Numerous studies have shown that circRNAs are aberrantly expressed in various cancers and play a significant role in tumor progression. However, the molecular mechanisms of circRNAs in triple-negative breast cancer (TNBC) remain ambiguous. By intersecting throughput data and qRT-PCR results from tissues and cell lines, circ-TRIO was identified as a potential oncogenic regulator of TNBC. Moreover, circ-TRIO expression was detected in TNBC tissues and was correlated with the recurrence and prognosis of TNBC patients. The circular characteristics of circ-TRIO were verified by RNase R and CHX assays. Functionally, the knockdown of circ-TRIO inhibited the proliferation, migration and invasion of TNBC cells, while the overexpression of circ-TRIO resulted in the opposite impacts. Mechanistically, a dual luciferase reporter assay and RNA immunoprecipitation were performed and indicated that circ-TRIO could combine with miR-432-5p to regulate the expression of coiled-coil domain containing 58 (CCDC58). In summary, our study illustrates that circ-TRIO plays an important role in the progression of TNBC by regulating the miR-432-5p/CCDC58 axis, which could broaden our insight into the underlying mechanisms and provide a novel prognostic marker of TNBC in the clinic. Nature Publishing Group UK 2022-09-08 /pmc/articles/PMC9458743/ /pubmed/36075896 http://dx.doi.org/10.1038/s41419-022-05216-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Wang, Zekun Li, Yaming Yang, Jingwen Liang, Yiran Wang, Xiaolong Zhang, Ning Kong, Xiaoli Chen, Bing Wang, Lijuan Zhao, Wenjing Yang, Qifeng Circ-TRIO promotes TNBC progression by regulating the miR-432-5p/CCDC58 axis |
title | Circ-TRIO promotes TNBC progression by regulating the miR-432-5p/CCDC58 axis |
title_full | Circ-TRIO promotes TNBC progression by regulating the miR-432-5p/CCDC58 axis |
title_fullStr | Circ-TRIO promotes TNBC progression by regulating the miR-432-5p/CCDC58 axis |
title_full_unstemmed | Circ-TRIO promotes TNBC progression by regulating the miR-432-5p/CCDC58 axis |
title_short | Circ-TRIO promotes TNBC progression by regulating the miR-432-5p/CCDC58 axis |
title_sort | circ-trio promotes tnbc progression by regulating the mir-432-5p/ccdc58 axis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9458743/ https://www.ncbi.nlm.nih.gov/pubmed/36075896 http://dx.doi.org/10.1038/s41419-022-05216-7 |
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