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Hsa_circ_0070963 inhibits liver fibrosis via regulation of miR-223-3p and LEMD3
Previous circular RNA (circRNA) microarray analyses have uncovered an abnormal expression of hsa_circ_0070963 in hepatic stellate cells (HSCs). However, the specific role of hsa_circ_0070963 in liver fibrosis remains unknown. Here, we show that hsa_circ_0070963 inhibits liver fibrosis via regulation...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7053641/ https://www.ncbi.nlm.nih.gov/pubmed/32003753 http://dx.doi.org/10.18632/aging.102705 |
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author | Ji, Dong Chen, Guo-Feng Wang, Jin-Cheng Ji, Si-Han Wu, Xue-Wen Lu, Xiao-Jie Chen, Jin-Lian Li, Jing-Tao |
author_facet | Ji, Dong Chen, Guo-Feng Wang, Jin-Cheng Ji, Si-Han Wu, Xue-Wen Lu, Xiao-Jie Chen, Jin-Lian Li, Jing-Tao |
author_sort | Ji, Dong |
collection | PubMed |
description | Previous circular RNA (circRNA) microarray analyses have uncovered an abnormal expression of hsa_circ_0070963 in hepatic stellate cells (HSCs). However, the specific role of hsa_circ_0070963 in liver fibrosis remains unknown. Here, we show that hsa_circ_0070963 inhibits liver fibrosis via regulation of miR-223-3p and LEMD3. Moreover, we demonstrated that hsa_circ_0070963 levels were reduced during liver fibrosis while restoring hsa_circ_0070963 levels abolished HSC activation, with a reduction in α-SMA and type I collagen levels both in vitro and in vivo. Furthermore, hsa_circ_0070963 overexpression suppressed both cell proliferation and the cell cycle of HSCs. MiR-223-3p was confirmed as a target of hsa_circ_0070963 and was shown to be involved in the effects of hsa_circ_0070963 on HSC activation. Furthermore, LEMD3 was confirmed as a target of miR-223-3p and was shown to be responsible for the activation of HSCs. The interactions between hsa_circ_0070963, miR-223-3p, and LEMD3 were validated via bioinformatic analysis, luciferase reporter assays, and rescue experiments. Collectively, hsa_circ_0070963 appeared to function as a miR-223-3p sponge that inhibited HSC activation in liver fibrosis via regulation of miR-223-3p and LEMD3. Therefore, hsa_circ_0070963 may serve as a potential therapeutic target for liver fibrosis. |
format | Online Article Text |
id | pubmed-7053641 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Impact Journals |
record_format | MEDLINE/PubMed |
spelling | pubmed-70536412020-03-12 Hsa_circ_0070963 inhibits liver fibrosis via regulation of miR-223-3p and LEMD3 Ji, Dong Chen, Guo-Feng Wang, Jin-Cheng Ji, Si-Han Wu, Xue-Wen Lu, Xiao-Jie Chen, Jin-Lian Li, Jing-Tao Aging (Albany NY) Research Paper Previous circular RNA (circRNA) microarray analyses have uncovered an abnormal expression of hsa_circ_0070963 in hepatic stellate cells (HSCs). However, the specific role of hsa_circ_0070963 in liver fibrosis remains unknown. Here, we show that hsa_circ_0070963 inhibits liver fibrosis via regulation of miR-223-3p and LEMD3. Moreover, we demonstrated that hsa_circ_0070963 levels were reduced during liver fibrosis while restoring hsa_circ_0070963 levels abolished HSC activation, with a reduction in α-SMA and type I collagen levels both in vitro and in vivo. Furthermore, hsa_circ_0070963 overexpression suppressed both cell proliferation and the cell cycle of HSCs. MiR-223-3p was confirmed as a target of hsa_circ_0070963 and was shown to be involved in the effects of hsa_circ_0070963 on HSC activation. Furthermore, LEMD3 was confirmed as a target of miR-223-3p and was shown to be responsible for the activation of HSCs. The interactions between hsa_circ_0070963, miR-223-3p, and LEMD3 were validated via bioinformatic analysis, luciferase reporter assays, and rescue experiments. Collectively, hsa_circ_0070963 appeared to function as a miR-223-3p sponge that inhibited HSC activation in liver fibrosis via regulation of miR-223-3p and LEMD3. Therefore, hsa_circ_0070963 may serve as a potential therapeutic target for liver fibrosis. Impact Journals 2020-01-29 /pmc/articles/PMC7053641/ /pubmed/32003753 http://dx.doi.org/10.18632/aging.102705 Text en Copyright © 2020 Ji et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Ji, Dong Chen, Guo-Feng Wang, Jin-Cheng Ji, Si-Han Wu, Xue-Wen Lu, Xiao-Jie Chen, Jin-Lian Li, Jing-Tao Hsa_circ_0070963 inhibits liver fibrosis via regulation of miR-223-3p and LEMD3 |
title | Hsa_circ_0070963 inhibits liver fibrosis via regulation of miR-223-3p and LEMD3 |
title_full | Hsa_circ_0070963 inhibits liver fibrosis via regulation of miR-223-3p and LEMD3 |
title_fullStr | Hsa_circ_0070963 inhibits liver fibrosis via regulation of miR-223-3p and LEMD3 |
title_full_unstemmed | Hsa_circ_0070963 inhibits liver fibrosis via regulation of miR-223-3p and LEMD3 |
title_short | Hsa_circ_0070963 inhibits liver fibrosis via regulation of miR-223-3p and LEMD3 |
title_sort | hsa_circ_0070963 inhibits liver fibrosis via regulation of mir-223-3p and lemd3 |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7053641/ https://www.ncbi.nlm.nih.gov/pubmed/32003753 http://dx.doi.org/10.18632/aging.102705 |
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