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Circular RNA hsa_circ_0007364 increases cervical cancer progression through activating methionine adenosyltransferase II alpha (MAT2A) expression by restraining microRNA-101-5p
Emerging evidence suggested that circular RNAs (circRNAs) play critical roles in cervical cancer (CC) progression. However, the roles and molecular mechanisms of hsa_circ_0007364 in the tumorigenesis of CC remain unclear. In the present study, we used bioinformatics analysis and a series of experime...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8291787/ https://www.ncbi.nlm.nih.gov/pubmed/33138667 http://dx.doi.org/10.1080/21655979.2020.1832343 |
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author | Chen, Hongfei Gu, Bin Zhao, Xiang Zhao, Yupeng Huo, Shuning Liu, Xiang Lu, Huihong |
author_facet | Chen, Hongfei Gu, Bin Zhao, Xiang Zhao, Yupeng Huo, Shuning Liu, Xiang Lu, Huihong |
author_sort | Chen, Hongfei |
collection | PubMed |
description | Emerging evidence suggested that circular RNAs (circRNAs) play critical roles in cervical cancer (CC) progression. However, the roles and molecular mechanisms of hsa_circ_0007364 in the tumorigenesis of CC remain unclear. In the present study, we used bioinformatics analysis and a series of experimental analysis to characterize a novel circRNA, hsa_circ_0007364 was up-regulated and associated with advanced clinical features in CC patients. Hsa_circ_0007364 inhibition notably suppressed the proliferation and invasion abilities of CC cells in vitro and reduced tumor growth in vivo. Moreover, hsa_circ_0007364 was uncovered to sponge miR-101-5p. Additionally, methionine adenosyltransferase II alpha (MAT2A) was verified as a target gene of miR-101-5p, and its downregulation reversed the inhibitory effects of hsa_circ_0007364 knockdown on CC progression. Therefore, we suggested that hsa_circ_0007364 might serve as an oncogenic circRNA in CC progression by regulating the miR-101-5p/MAT2A axis, which provides a potential therapeutic target to the treatment. Research highlights 1. hsa_circ_0007364 was upregulated in CC; 2. hsa_circ_0007364 promoted CC cell progression; 3. hsa_circ_0007364/miR-101-5p/MAT2A axis in CC. |
format | Online Article Text |
id | pubmed-8291787 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-82917872021-09-01 Circular RNA hsa_circ_0007364 increases cervical cancer progression through activating methionine adenosyltransferase II alpha (MAT2A) expression by restraining microRNA-101-5p Chen, Hongfei Gu, Bin Zhao, Xiang Zhao, Yupeng Huo, Shuning Liu, Xiang Lu, Huihong Bioengineered Research Paper Emerging evidence suggested that circular RNAs (circRNAs) play critical roles in cervical cancer (CC) progression. However, the roles and molecular mechanisms of hsa_circ_0007364 in the tumorigenesis of CC remain unclear. In the present study, we used bioinformatics analysis and a series of experimental analysis to characterize a novel circRNA, hsa_circ_0007364 was up-regulated and associated with advanced clinical features in CC patients. Hsa_circ_0007364 inhibition notably suppressed the proliferation and invasion abilities of CC cells in vitro and reduced tumor growth in vivo. Moreover, hsa_circ_0007364 was uncovered to sponge miR-101-5p. Additionally, methionine adenosyltransferase II alpha (MAT2A) was verified as a target gene of miR-101-5p, and its downregulation reversed the inhibitory effects of hsa_circ_0007364 knockdown on CC progression. Therefore, we suggested that hsa_circ_0007364 might serve as an oncogenic circRNA in CC progression by regulating the miR-101-5p/MAT2A axis, which provides a potential therapeutic target to the treatment. Research highlights 1. hsa_circ_0007364 was upregulated in CC; 2. hsa_circ_0007364 promoted CC cell progression; 3. hsa_circ_0007364/miR-101-5p/MAT2A axis in CC. Taylor & Francis 2020-11-02 /pmc/articles/PMC8291787/ /pubmed/33138667 http://dx.doi.org/10.1080/21655979.2020.1832343 Text en © 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Paper Chen, Hongfei Gu, Bin Zhao, Xiang Zhao, Yupeng Huo, Shuning Liu, Xiang Lu, Huihong Circular RNA hsa_circ_0007364 increases cervical cancer progression through activating methionine adenosyltransferase II alpha (MAT2A) expression by restraining microRNA-101-5p |
title | Circular RNA hsa_circ_0007364 increases cervical cancer progression through activating methionine adenosyltransferase II alpha (MAT2A) expression by restraining microRNA-101-5p |
title_full | Circular RNA hsa_circ_0007364 increases cervical cancer progression through activating methionine adenosyltransferase II alpha (MAT2A) expression by restraining microRNA-101-5p |
title_fullStr | Circular RNA hsa_circ_0007364 increases cervical cancer progression through activating methionine adenosyltransferase II alpha (MAT2A) expression by restraining microRNA-101-5p |
title_full_unstemmed | Circular RNA hsa_circ_0007364 increases cervical cancer progression through activating methionine adenosyltransferase II alpha (MAT2A) expression by restraining microRNA-101-5p |
title_short | Circular RNA hsa_circ_0007364 increases cervical cancer progression through activating methionine adenosyltransferase II alpha (MAT2A) expression by restraining microRNA-101-5p |
title_sort | circular rna hsa_circ_0007364 increases cervical cancer progression through activating methionine adenosyltransferase ii alpha (mat2a) expression by restraining microrna-101-5p |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8291787/ https://www.ncbi.nlm.nih.gov/pubmed/33138667 http://dx.doi.org/10.1080/21655979.2020.1832343 |
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