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Circ_0003570 Suppresses the progression of hepatocellular carcinoma through miR-182-5p/STARD13 regulatory axis

BACKGROUND: Emerging evidence have revealed that circRNAs exert important biological effects in the development and progression of various diseases, including cancer. Our study aimed to elaborated the biological effects of hsa-circ_0003570 in hepatocellular carcinoma (HCC) development at the molecul...

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Autores principales: Zhang, Xu, Chen, Wenwen, Guo, Dan, Li, Yarui, Zhao, Yan, Ren, Mudan, Lu, Guifang, Lu, Xinlan, He, Shuixiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9563790/
https://www.ncbi.nlm.nih.gov/pubmed/36241975
http://dx.doi.org/10.1186/s12575-022-00176-w
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author Zhang, Xu
Chen, Wenwen
Guo, Dan
Li, Yarui
Zhao, Yan
Ren, Mudan
Lu, Guifang
Lu, Xinlan
He, Shuixiang
author_facet Zhang, Xu
Chen, Wenwen
Guo, Dan
Li, Yarui
Zhao, Yan
Ren, Mudan
Lu, Guifang
Lu, Xinlan
He, Shuixiang
author_sort Zhang, Xu
collection PubMed
description BACKGROUND: Emerging evidence have revealed that circRNAs exert important biological effects in the development and progression of various diseases, including cancer. Our study aimed to elaborated the biological effects of hsa-circ_0003570 in hepatocellular carcinoma (HCC) development at the molecular level. RESULTS: The results of functional experiments showed that knockdown of circ_0003570 induced HCC cell growth, migration and invasion, whereas overexpression of circ_0003570 presented the opposite effects. In vivo experiments, xenograft tumors grown from circ-overexpressed cells had smaller tumor volume and weight than the control group. Further investigations suggested that circ_0003570 may function as a competing endogenous RNA via competitively binding miR-182-5p and thereby regulating the repression of downstream target gene STARD13, which were demonstrated by dual luciferase reporter assay and functional rescued experiments. CONCLUSIONS: Taken together, circ_0003570 suppresses the development of HCC by modulating miR-182-5p/STARD13 axis. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12575-022-00176-w.
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spelling pubmed-95637902022-10-15 Circ_0003570 Suppresses the progression of hepatocellular carcinoma through miR-182-5p/STARD13 regulatory axis Zhang, Xu Chen, Wenwen Guo, Dan Li, Yarui Zhao, Yan Ren, Mudan Lu, Guifang Lu, Xinlan He, Shuixiang Biol Proced Online Research BACKGROUND: Emerging evidence have revealed that circRNAs exert important biological effects in the development and progression of various diseases, including cancer. Our study aimed to elaborated the biological effects of hsa-circ_0003570 in hepatocellular carcinoma (HCC) development at the molecular level. RESULTS: The results of functional experiments showed that knockdown of circ_0003570 induced HCC cell growth, migration and invasion, whereas overexpression of circ_0003570 presented the opposite effects. In vivo experiments, xenograft tumors grown from circ-overexpressed cells had smaller tumor volume and weight than the control group. Further investigations suggested that circ_0003570 may function as a competing endogenous RNA via competitively binding miR-182-5p and thereby regulating the repression of downstream target gene STARD13, which were demonstrated by dual luciferase reporter assay and functional rescued experiments. CONCLUSIONS: Taken together, circ_0003570 suppresses the development of HCC by modulating miR-182-5p/STARD13 axis. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12575-022-00176-w. BioMed Central 2022-10-14 /pmc/articles/PMC9563790/ /pubmed/36241975 http://dx.doi.org/10.1186/s12575-022-00176-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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 Research
Zhang, Xu
Chen, Wenwen
Guo, Dan
Li, Yarui
Zhao, Yan
Ren, Mudan
Lu, Guifang
Lu, Xinlan
He, Shuixiang
Circ_0003570 Suppresses the progression of hepatocellular carcinoma through miR-182-5p/STARD13 regulatory axis
title Circ_0003570 Suppresses the progression of hepatocellular carcinoma through miR-182-5p/STARD13 regulatory axis
title_full Circ_0003570 Suppresses the progression of hepatocellular carcinoma through miR-182-5p/STARD13 regulatory axis
title_fullStr Circ_0003570 Suppresses the progression of hepatocellular carcinoma through miR-182-5p/STARD13 regulatory axis
title_full_unstemmed Circ_0003570 Suppresses the progression of hepatocellular carcinoma through miR-182-5p/STARD13 regulatory axis
title_short Circ_0003570 Suppresses the progression of hepatocellular carcinoma through miR-182-5p/STARD13 regulatory axis
title_sort circ_0003570 suppresses the progression of hepatocellular carcinoma through mir-182-5p/stard13 regulatory axis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9563790/
https://www.ncbi.nlm.nih.gov/pubmed/36241975
http://dx.doi.org/10.1186/s12575-022-00176-w
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