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miRNA-1284, a regulator of HMGB1, inhibits cell proliferation and migration in osteosarcoma
Previous literatures have reported the role of human micro RNA-1284 (hsa-miR-1284, in short miR-1284) in diverse cancers. However, its biological function in osteosarcoma pathogenesis remains unknown. In the present study, we investigated the potential role of miR-1284 in osteosarcoma. Expression of...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Portland Press Ltd.
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6043716/ https://www.ncbi.nlm.nih.gov/pubmed/29899164 http://dx.doi.org/10.1042/BSR20171675 |
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author | Lv, Shuai Guan, Meng |
author_facet | Lv, Shuai Guan, Meng |
author_sort | Lv, Shuai |
collection | PubMed |
description | Previous literatures have reported the role of human micro RNA-1284 (hsa-miR-1284, in short miR-1284) in diverse cancers. However, its biological function in osteosarcoma pathogenesis remains unknown. In the present study, we investigated the potential role of miR-1284 in osteosarcoma. Expression of miR-1284 and high mobility group box 1 (HMGB1) were examined in 80 tissues obtained from 40 patients. MiR-1284 level was measured in five osteosarcoma cell lines. Relative luciferase activity and HMGB1 expression were examined in MG-63 and U2OS cells transfected with wild-type or mutant 3′-UTR of HMGB1 in the presence of miR-1284 mimics or miR-NC. Cell viability, colony formation, and cell migration were measured in MG-63, U2OS and hFOB 1.19 cells, which were transfected with miR-1284 mimics or miR-NC. In the rescue experiments, recombinant HMGB1 plasmid was transfected into MG-63 and U2OS cells, and cell viability and migration were determined again. Our results indicated that relative level of miR-1284 was lower in tumor tissues compared with its adjacent tissues and it was found suppressed at lower levels in MG-63 and U2OS cell lines. Expression of HMGB1 is significantly elevated in tumor tissues and negatively correlated with miR-1284 expression. MiR-1284 exerted its function by directly binding to 3′-UTR of HMGB1 and regulates expression of HMGB1. The overexpression of miR-1284 inhibited the cell proliferation and migration, and altered the protein expression of epithelial–mesenchymal transition (EMT)-associated genes (E-cadherin, N-cadherin, Vimentin, and Snail), which was reversed by HMGB1 overexpression. In conclusion, miR-1284 can function as a new regulator to inhibit osteosarcoma cell proliferation and migration by targeting HMGB1. |
format | Online Article Text |
id | pubmed-6043716 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Portland Press Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-60437162018-07-18 miRNA-1284, a regulator of HMGB1, inhibits cell proliferation and migration in osteosarcoma Lv, Shuai Guan, Meng Biosci Rep Research Articles Previous literatures have reported the role of human micro RNA-1284 (hsa-miR-1284, in short miR-1284) in diverse cancers. However, its biological function in osteosarcoma pathogenesis remains unknown. In the present study, we investigated the potential role of miR-1284 in osteosarcoma. Expression of miR-1284 and high mobility group box 1 (HMGB1) were examined in 80 tissues obtained from 40 patients. MiR-1284 level was measured in five osteosarcoma cell lines. Relative luciferase activity and HMGB1 expression were examined in MG-63 and U2OS cells transfected with wild-type or mutant 3′-UTR of HMGB1 in the presence of miR-1284 mimics or miR-NC. Cell viability, colony formation, and cell migration were measured in MG-63, U2OS and hFOB 1.19 cells, which were transfected with miR-1284 mimics or miR-NC. In the rescue experiments, recombinant HMGB1 plasmid was transfected into MG-63 and U2OS cells, and cell viability and migration were determined again. Our results indicated that relative level of miR-1284 was lower in tumor tissues compared with its adjacent tissues and it was found suppressed at lower levels in MG-63 and U2OS cell lines. Expression of HMGB1 is significantly elevated in tumor tissues and negatively correlated with miR-1284 expression. MiR-1284 exerted its function by directly binding to 3′-UTR of HMGB1 and regulates expression of HMGB1. The overexpression of miR-1284 inhibited the cell proliferation and migration, and altered the protein expression of epithelial–mesenchymal transition (EMT)-associated genes (E-cadherin, N-cadherin, Vimentin, and Snail), which was reversed by HMGB1 overexpression. In conclusion, miR-1284 can function as a new regulator to inhibit osteosarcoma cell proliferation and migration by targeting HMGB1. Portland Press Ltd. 2018-07-13 /pmc/articles/PMC6043716/ /pubmed/29899164 http://dx.doi.org/10.1042/BSR20171675 Text en © 2018 The Author(s). http://creativecommons.org/licenses/by/4.0/This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) (http://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Articles Lv, Shuai Guan, Meng miRNA-1284, a regulator of HMGB1, inhibits cell proliferation and migration in osteosarcoma |
title | miRNA-1284, a regulator of HMGB1, inhibits cell proliferation and migration in osteosarcoma |
title_full | miRNA-1284, a regulator of HMGB1, inhibits cell proliferation and migration in osteosarcoma |
title_fullStr | miRNA-1284, a regulator of HMGB1, inhibits cell proliferation and migration in osteosarcoma |
title_full_unstemmed | miRNA-1284, a regulator of HMGB1, inhibits cell proliferation and migration in osteosarcoma |
title_short | miRNA-1284, a regulator of HMGB1, inhibits cell proliferation and migration in osteosarcoma |
title_sort | mirna-1284, a regulator of hmgb1, inhibits cell proliferation and migration in osteosarcoma |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6043716/ https://www.ncbi.nlm.nih.gov/pubmed/29899164 http://dx.doi.org/10.1042/BSR20171675 |
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