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Intergenic CircRNA Circ_0007379 Inhibits Colorectal Cancer Progression by Modulating miR-320a Biogenesis in a KSRP-Dependent Manner
Circular RNAs (circRNAs) are covalently closed RNA structures that play multiple roles in tumorigenesis and progression. Compared with exon‒intron circRNAs, the biological functions and implications of intergenic circRNAs in human cancer are still poorly understood. Here, we performed circRNA microa...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10411474/ https://www.ncbi.nlm.nih.gov/pubmed/37564198 http://dx.doi.org/10.7150/ijbs.85063 |
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author | Long, Fei Li, Liang Xie, Canbin Ma, Min Wu, Zhiwei Lu, Zhixing Liu, Baiying Yang, Ming Zhang, Fan Ning, Zhengping Zhong, Chonglei Yu, Bowen Liu, Shiyi Wan, Longyu Tian, Buning Yang, Kaiyan Guo, Yihang Chen, Miao Chou, Jin Li, Xiaorong Hu, Gui Lin, Changwei Zhang, Yi |
author_facet | Long, Fei Li, Liang Xie, Canbin Ma, Min Wu, Zhiwei Lu, Zhixing Liu, Baiying Yang, Ming Zhang, Fan Ning, Zhengping Zhong, Chonglei Yu, Bowen Liu, Shiyi Wan, Longyu Tian, Buning Yang, Kaiyan Guo, Yihang Chen, Miao Chou, Jin Li, Xiaorong Hu, Gui Lin, Changwei Zhang, Yi |
author_sort | Long, Fei |
collection | PubMed |
description | Circular RNAs (circRNAs) are covalently closed RNA structures that play multiple roles in tumorigenesis and progression. Compared with exon‒intron circRNAs, the biological functions and implications of intergenic circRNAs in human cancer are still poorly understood. Here, we performed circRNA microarray analysis and identified an intergenic circRNA, circ_0007379, that was significantly downregulated in patients with colorectal cancer (CRC). The biogenesis of circ_0007379 was mediated by reverse complementary matches (RCMs) and was negatively regulated by the RNA helicase DHX9. Functionally, circ_0007379 suppressed CRC cell growth and metastasis in cell culture as well as in patient-derived organoid and xenograft models. Mechanistically, circ_0007379 acted as a scaffold to facilitate the processing of both pri-miR-320a and pre-miR-320a in a KSRP-dependent manner, leading to miR-320a maturation and subsequent repression of transcription factor RUNX1 expression. Thus, our findings establish a previously unrecognized function of circRNA in inhibiting CRC progression. |
format | Online Article Text |
id | pubmed-10411474 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-104114742023-08-10 Intergenic CircRNA Circ_0007379 Inhibits Colorectal Cancer Progression by Modulating miR-320a Biogenesis in a KSRP-Dependent Manner Long, Fei Li, Liang Xie, Canbin Ma, Min Wu, Zhiwei Lu, Zhixing Liu, Baiying Yang, Ming Zhang, Fan Ning, Zhengping Zhong, Chonglei Yu, Bowen Liu, Shiyi Wan, Longyu Tian, Buning Yang, Kaiyan Guo, Yihang Chen, Miao Chou, Jin Li, Xiaorong Hu, Gui Lin, Changwei Zhang, Yi Int J Biol Sci Research Paper Circular RNAs (circRNAs) are covalently closed RNA structures that play multiple roles in tumorigenesis and progression. Compared with exon‒intron circRNAs, the biological functions and implications of intergenic circRNAs in human cancer are still poorly understood. Here, we performed circRNA microarray analysis and identified an intergenic circRNA, circ_0007379, that was significantly downregulated in patients with colorectal cancer (CRC). The biogenesis of circ_0007379 was mediated by reverse complementary matches (RCMs) and was negatively regulated by the RNA helicase DHX9. Functionally, circ_0007379 suppressed CRC cell growth and metastasis in cell culture as well as in patient-derived organoid and xenograft models. Mechanistically, circ_0007379 acted as a scaffold to facilitate the processing of both pri-miR-320a and pre-miR-320a in a KSRP-dependent manner, leading to miR-320a maturation and subsequent repression of transcription factor RUNX1 expression. Thus, our findings establish a previously unrecognized function of circRNA in inhibiting CRC progression. Ivyspring International Publisher 2023-07-24 /pmc/articles/PMC10411474/ /pubmed/37564198 http://dx.doi.org/10.7150/ijbs.85063 Text en © The author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions. |
spellingShingle | Research Paper Long, Fei Li, Liang Xie, Canbin Ma, Min Wu, Zhiwei Lu, Zhixing Liu, Baiying Yang, Ming Zhang, Fan Ning, Zhengping Zhong, Chonglei Yu, Bowen Liu, Shiyi Wan, Longyu Tian, Buning Yang, Kaiyan Guo, Yihang Chen, Miao Chou, Jin Li, Xiaorong Hu, Gui Lin, Changwei Zhang, Yi Intergenic CircRNA Circ_0007379 Inhibits Colorectal Cancer Progression by Modulating miR-320a Biogenesis in a KSRP-Dependent Manner |
title | Intergenic CircRNA Circ_0007379 Inhibits Colorectal Cancer Progression by Modulating miR-320a Biogenesis in a KSRP-Dependent Manner |
title_full | Intergenic CircRNA Circ_0007379 Inhibits Colorectal Cancer Progression by Modulating miR-320a Biogenesis in a KSRP-Dependent Manner |
title_fullStr | Intergenic CircRNA Circ_0007379 Inhibits Colorectal Cancer Progression by Modulating miR-320a Biogenesis in a KSRP-Dependent Manner |
title_full_unstemmed | Intergenic CircRNA Circ_0007379 Inhibits Colorectal Cancer Progression by Modulating miR-320a Biogenesis in a KSRP-Dependent Manner |
title_short | Intergenic CircRNA Circ_0007379 Inhibits Colorectal Cancer Progression by Modulating miR-320a Biogenesis in a KSRP-Dependent Manner |
title_sort | intergenic circrna circ_0007379 inhibits colorectal cancer progression by modulating mir-320a biogenesis in a ksrp-dependent manner |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10411474/ https://www.ncbi.nlm.nih.gov/pubmed/37564198 http://dx.doi.org/10.7150/ijbs.85063 |
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