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miR-34a suppresses proliferation and induces apoptosis of human lens epithelial cells by targeting E2F3
microRNA (miRNA) is abnormally expressed in numerous diseases, and it was intimately associated with cell proliferation and apoptosis. However, the mechanism by which miRNAs control cataractogenesis remains unclear. In the current study, it was demonstrated that miR-34a was highly expressed in the c...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5355663/ https://www.ncbi.nlm.nih.gov/pubmed/27840975 http://dx.doi.org/10.3892/mmr.2016.5901 |
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author | Xiang, Wu Lin, Haotian Wang, Qilin Chen, Wan Liu, Zhaochuan Chen, Hui Zhang, Hui Chen, Weirong |
author_facet | Xiang, Wu Lin, Haotian Wang, Qilin Chen, Wan Liu, Zhaochuan Chen, Hui Zhang, Hui Chen, Weirong |
author_sort | Xiang, Wu |
collection | PubMed |
description | microRNA (miRNA) is abnormally expressed in numerous diseases, and it was intimately associated with cell proliferation and apoptosis. However, the mechanism by which miRNAs control cataractogenesis remains unclear. In the current study, it was demonstrated that miR-34a was highly expressed in the cataractous lens by stem-loop reverse transcription-quantitative polymerase chain reaction. Trying to investigate the role of miR-34a in human lens epithelial cells, miR-34a mimics were transfected into SRA01/04 cells, and this suppressed proliferation and induced apoptosis. Subsequently, E2F3 was confirmed as a direct target of miR-34a. Downregulation of E2F3 by small interfering (si) RNA siE2F3 resulted in proliferation inhibition and apoptosis of SRA01/04 cells. Furthermore, it was demonstrated that miR-34a and siE2F3 downregulated E2F3 expression at a protein level. In summary, the current study demonstrated that miR-34a suppressed the proliferation and induced apoptosis of SRA01/04 cells by downregulating E2F3. These observations provide novel insights with potential therapeutic applications for the treatment of cataracts. |
format | Online Article Text |
id | pubmed-5355663 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-53556632017-03-31 miR-34a suppresses proliferation and induces apoptosis of human lens epithelial cells by targeting E2F3 Xiang, Wu Lin, Haotian Wang, Qilin Chen, Wan Liu, Zhaochuan Chen, Hui Zhang, Hui Chen, Weirong Mol Med Rep Articles microRNA (miRNA) is abnormally expressed in numerous diseases, and it was intimately associated with cell proliferation and apoptosis. However, the mechanism by which miRNAs control cataractogenesis remains unclear. In the current study, it was demonstrated that miR-34a was highly expressed in the cataractous lens by stem-loop reverse transcription-quantitative polymerase chain reaction. Trying to investigate the role of miR-34a in human lens epithelial cells, miR-34a mimics were transfected into SRA01/04 cells, and this suppressed proliferation and induced apoptosis. Subsequently, E2F3 was confirmed as a direct target of miR-34a. Downregulation of E2F3 by small interfering (si) RNA siE2F3 resulted in proliferation inhibition and apoptosis of SRA01/04 cells. Furthermore, it was demonstrated that miR-34a and siE2F3 downregulated E2F3 expression at a protein level. In summary, the current study demonstrated that miR-34a suppressed the proliferation and induced apoptosis of SRA01/04 cells by downregulating E2F3. These observations provide novel insights with potential therapeutic applications for the treatment of cataracts. D.A. Spandidos 2016-12 2016-10-27 /pmc/articles/PMC5355663/ /pubmed/27840975 http://dx.doi.org/10.3892/mmr.2016.5901 Text en Copyright: © Xiang et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Xiang, Wu Lin, Haotian Wang, Qilin Chen, Wan Liu, Zhaochuan Chen, Hui Zhang, Hui Chen, Weirong miR-34a suppresses proliferation and induces apoptosis of human lens epithelial cells by targeting E2F3 |
title | miR-34a suppresses proliferation and induces apoptosis of human lens epithelial cells by targeting E2F3 |
title_full | miR-34a suppresses proliferation and induces apoptosis of human lens epithelial cells by targeting E2F3 |
title_fullStr | miR-34a suppresses proliferation and induces apoptosis of human lens epithelial cells by targeting E2F3 |
title_full_unstemmed | miR-34a suppresses proliferation and induces apoptosis of human lens epithelial cells by targeting E2F3 |
title_short | miR-34a suppresses proliferation and induces apoptosis of human lens epithelial cells by targeting E2F3 |
title_sort | mir-34a suppresses proliferation and induces apoptosis of human lens epithelial cells by targeting e2f3 |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5355663/ https://www.ncbi.nlm.nih.gov/pubmed/27840975 http://dx.doi.org/10.3892/mmr.2016.5901 |
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