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Circular RNA hsa_Circ_101141 as a Competing Endogenous RNA Facilitates Tumorigenesis of Hepatocellular Carcinoma by Regulating miR-1297/ROCK1 Pathway
As a novel class of noncoding RNAs, circular RNAs (circRNAs) have been recently reported to be involved in cell development and function. However, the functional role of circRNAs in hepatocellular carcinoma (HCC) remains unclear. In the present study, we found that the expression of human circ_10114...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7563807/ https://www.ncbi.nlm.nih.gov/pubmed/32787581 http://dx.doi.org/10.1177/0963689720948016 |
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author | Zhang, Tao Zhang, Lijuan Han, Dan Tursun, Kebinur Lu, Xiaobo |
author_facet | Zhang, Tao Zhang, Lijuan Han, Dan Tursun, Kebinur Lu, Xiaobo |
author_sort | Zhang, Tao |
collection | PubMed |
description | As a novel class of noncoding RNAs, circular RNAs (circRNAs) have been recently reported to be involved in cell development and function. However, the functional role of circRNAs in hepatocellular carcinoma (HCC) remains unclear. In the present study, we found that the expression of human circ_101141 was upregulated in HCC tissues and cells. In addition, downregulation of circ_101141 dramatically inhibited cell proliferation, migration, and invasion in HCC cells. In addition, by using the bioinformatics tools, the potential target of circ_101141 was predicted. Mechanistic investigations indicated that circ_101141 acted as a miR-1297 “sponge”; meanwhile, Rho-associated, coiled-coil-containing protein kinase 1 (ROCK1) was a direct target of miR-1297. Further experiments demonstrated that circ_101141 contributed to the progression of HCC by acting as competing endogenous RNA (ceRNA) of miR-1297 to regulate ROCK1 expression. Furthermore, knockdown of circ_101141 attenuated HCC tumorigenesis in vivo. Taken together, these findings indicated that circRNA circ_101141 acted as a ceRNA to facilitate tumorigenesis of HCC by regulating miR-1297/ROCK1 pathway. |
format | Online Article Text |
id | pubmed-7563807 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-75638072020-10-26 Circular RNA hsa_Circ_101141 as a Competing Endogenous RNA Facilitates Tumorigenesis of Hepatocellular Carcinoma by Regulating miR-1297/ROCK1 Pathway Zhang, Tao Zhang, Lijuan Han, Dan Tursun, Kebinur Lu, Xiaobo Cell Transplant Original Article As a novel class of noncoding RNAs, circular RNAs (circRNAs) have been recently reported to be involved in cell development and function. However, the functional role of circRNAs in hepatocellular carcinoma (HCC) remains unclear. In the present study, we found that the expression of human circ_101141 was upregulated in HCC tissues and cells. In addition, downregulation of circ_101141 dramatically inhibited cell proliferation, migration, and invasion in HCC cells. In addition, by using the bioinformatics tools, the potential target of circ_101141 was predicted. Mechanistic investigations indicated that circ_101141 acted as a miR-1297 “sponge”; meanwhile, Rho-associated, coiled-coil-containing protein kinase 1 (ROCK1) was a direct target of miR-1297. Further experiments demonstrated that circ_101141 contributed to the progression of HCC by acting as competing endogenous RNA (ceRNA) of miR-1297 to regulate ROCK1 expression. Furthermore, knockdown of circ_101141 attenuated HCC tumorigenesis in vivo. Taken together, these findings indicated that circRNA circ_101141 acted as a ceRNA to facilitate tumorigenesis of HCC by regulating miR-1297/ROCK1 pathway. SAGE Publications 2020-08-13 /pmc/articles/PMC7563807/ /pubmed/32787581 http://dx.doi.org/10.1177/0963689720948016 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Article Zhang, Tao Zhang, Lijuan Han, Dan Tursun, Kebinur Lu, Xiaobo Circular RNA hsa_Circ_101141 as a Competing Endogenous RNA Facilitates Tumorigenesis of Hepatocellular Carcinoma by Regulating miR-1297/ROCK1 Pathway |
title | Circular RNA hsa_Circ_101141 as a Competing Endogenous RNA
Facilitates Tumorigenesis of Hepatocellular Carcinoma by Regulating
miR-1297/ROCK1 Pathway |
title_full | Circular RNA hsa_Circ_101141 as a Competing Endogenous RNA
Facilitates Tumorigenesis of Hepatocellular Carcinoma by Regulating
miR-1297/ROCK1 Pathway |
title_fullStr | Circular RNA hsa_Circ_101141 as a Competing Endogenous RNA
Facilitates Tumorigenesis of Hepatocellular Carcinoma by Regulating
miR-1297/ROCK1 Pathway |
title_full_unstemmed | Circular RNA hsa_Circ_101141 as a Competing Endogenous RNA
Facilitates Tumorigenesis of Hepatocellular Carcinoma by Regulating
miR-1297/ROCK1 Pathway |
title_short | Circular RNA hsa_Circ_101141 as a Competing Endogenous RNA
Facilitates Tumorigenesis of Hepatocellular Carcinoma by Regulating
miR-1297/ROCK1 Pathway |
title_sort | circular rna hsa_circ_101141 as a competing endogenous rna
facilitates tumorigenesis of hepatocellular carcinoma by regulating
mir-1297/rock1 pathway |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7563807/ https://www.ncbi.nlm.nih.gov/pubmed/32787581 http://dx.doi.org/10.1177/0963689720948016 |
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