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miR-454 functions as an oncogene by inhibiting CHD5 in hepatocellular carcinoma
Previous studies showed that miR-454 acted as an oncogene or tumor suppressor in cancer. However, its function in HCC remains unknown. In this study, we found that miR-454 expression was upregulated in HCC cell lines and tissues. Knockdown of miR-454 inhibited HCC cell proliferation and invasion and...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4770768/ https://www.ncbi.nlm.nih.gov/pubmed/26287602 |
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author | Yu, Lei Gong, Xuejun Sun, Lei Yao, Hong Lu, Baoling Zhu, Liying |
author_facet | Yu, Lei Gong, Xuejun Sun, Lei Yao, Hong Lu, Baoling Zhu, Liying |
author_sort | Yu, Lei |
collection | PubMed |
description | Previous studies showed that miR-454 acted as an oncogene or tumor suppressor in cancer. However, its function in HCC remains unknown. In this study, we found that miR-454 expression was upregulated in HCC cell lines and tissues. Knockdown of miR-454 inhibited HCC cell proliferation and invasion and epithelial mesenchymal transition (EMT), whereas overexpression of miR-454 promoted HCC cell proliferation and invasion and EMT. Furthermore, we identified the CHD5 as a direct target of miR-454. CHD5 was downregulated in HCC tissues and cell lines and the expression level of CHD5 was inversely correlated with the expression of miR-454 in HCC tissues. In addition, knockdown of miR-454 inhibited the growth of HepG2-engrafted tumors in vivo. Taken together, these results indicated that miR-454 functioned as an oncogene in HCC. |
format | Online Article Text |
id | pubmed-4770768 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-47707682016-03-21 miR-454 functions as an oncogene by inhibiting CHD5 in hepatocellular carcinoma Yu, Lei Gong, Xuejun Sun, Lei Yao, Hong Lu, Baoling Zhu, Liying Oncotarget Research Paper Previous studies showed that miR-454 acted as an oncogene or tumor suppressor in cancer. However, its function in HCC remains unknown. In this study, we found that miR-454 expression was upregulated in HCC cell lines and tissues. Knockdown of miR-454 inhibited HCC cell proliferation and invasion and epithelial mesenchymal transition (EMT), whereas overexpression of miR-454 promoted HCC cell proliferation and invasion and EMT. Furthermore, we identified the CHD5 as a direct target of miR-454. CHD5 was downregulated in HCC tissues and cell lines and the expression level of CHD5 was inversely correlated with the expression of miR-454 in HCC tissues. In addition, knockdown of miR-454 inhibited the growth of HepG2-engrafted tumors in vivo. Taken together, these results indicated that miR-454 functioned as an oncogene in HCC. Impact Journals LLC 2015-07-30 /pmc/articles/PMC4770768/ /pubmed/26287602 Text en Copyright: © 2015 Yu et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Yu, Lei Gong, Xuejun Sun, Lei Yao, Hong Lu, Baoling Zhu, Liying miR-454 functions as an oncogene by inhibiting CHD5 in hepatocellular carcinoma |
title | miR-454 functions as an oncogene by inhibiting CHD5 in hepatocellular carcinoma |
title_full | miR-454 functions as an oncogene by inhibiting CHD5 in hepatocellular carcinoma |
title_fullStr | miR-454 functions as an oncogene by inhibiting CHD5 in hepatocellular carcinoma |
title_full_unstemmed | miR-454 functions as an oncogene by inhibiting CHD5 in hepatocellular carcinoma |
title_short | miR-454 functions as an oncogene by inhibiting CHD5 in hepatocellular carcinoma |
title_sort | mir-454 functions as an oncogene by inhibiting chd5 in hepatocellular carcinoma |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4770768/ https://www.ncbi.nlm.nih.gov/pubmed/26287602 |
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