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Prognostic value of hsa-mir-299 and hsa-mir-7706 in hepatocellular carcinoma
This study aimed to investigate the expression of microRNA (miRNA) 299 and miRNA-7706 in patients with hepatocellular carcinoma (HCC), and to explore their effects on proliferation of SK-HEP-1 HCC cells. Expression of miRNA-299 and miRNA-7706 in tumor tissue (HCC group) and adjacent healthy tissue (...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6019942/ https://www.ncbi.nlm.nih.gov/pubmed/29963149 http://dx.doi.org/10.3892/ol.2018.8710 |
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author | Wang, Fenglin Dai, Min Chen, Hongjie Li, Yue Zhang, Jiongshan Zou, Zengcheng Yang, Hongzhi |
author_facet | Wang, Fenglin Dai, Min Chen, Hongjie Li, Yue Zhang, Jiongshan Zou, Zengcheng Yang, Hongzhi |
author_sort | Wang, Fenglin |
collection | PubMed |
description | This study aimed to investigate the expression of microRNA (miRNA) 299 and miRNA-7706 in patients with hepatocellular carcinoma (HCC), and to explore their effects on proliferation of SK-HEP-1 HCC cells. Expression of miRNA-299 and miRNA-7706 in tumor tissue (HCC group) and adjacent healthy tissue (>30 mm away from the tumor tissue) of 179 patients with HCC was determined by real-time polymerase chain reaction (qRT-PCR). miR-299 mimics and miR-7706 mimics were transfected into SK-HEP-1 HCC cells by RNA transfection. The proliferation and invasion of SK-HEP-1 cells were detected by CCK-8 kit and Transwell kit, respectively. Compared with adjacent tissues, expression levels of miRNA-299 and miRNA-7706 in HCC group were significantly downregulated. Analyses on the correlation between the expression of miRNA-299 and miRNA-7706 and clinical factors showed that expression levels of miRNA-299 and miRNA-7706 were significantly correlated with pathological stages and lymph node metastasis. ROC curve analysis showed that the areas under the curve were 0.837 and 0.845 for miRNA-299 and miRNA-7706 in the prediction of HCC, respectively. Survival analysis showed that the 5-year overall survival rate of patients with high expression levels of miRNA-299 and miRNA-7706 was significantly different from that of patients with low expression levels (P=0.016). Compared with cells transfected with scramble mimics, proliferation and invasion abilities of SK-HEP-1 cells transfected with miR-299 mimics and miRNA-7706 were significantly weakened. Results suggested that downregulation of miRNA-299 and miRNA-7706 can inhibit the proliferation of HCC cells and can be used as a new target for the treatment of HCC. |
format | Online Article Text |
id | pubmed-6019942 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-60199422018-06-29 Prognostic value of hsa-mir-299 and hsa-mir-7706 in hepatocellular carcinoma Wang, Fenglin Dai, Min Chen, Hongjie Li, Yue Zhang, Jiongshan Zou, Zengcheng Yang, Hongzhi Oncol Lett Articles This study aimed to investigate the expression of microRNA (miRNA) 299 and miRNA-7706 in patients with hepatocellular carcinoma (HCC), and to explore their effects on proliferation of SK-HEP-1 HCC cells. Expression of miRNA-299 and miRNA-7706 in tumor tissue (HCC group) and adjacent healthy tissue (>30 mm away from the tumor tissue) of 179 patients with HCC was determined by real-time polymerase chain reaction (qRT-PCR). miR-299 mimics and miR-7706 mimics were transfected into SK-HEP-1 HCC cells by RNA transfection. The proliferation and invasion of SK-HEP-1 cells were detected by CCK-8 kit and Transwell kit, respectively. Compared with adjacent tissues, expression levels of miRNA-299 and miRNA-7706 in HCC group were significantly downregulated. Analyses on the correlation between the expression of miRNA-299 and miRNA-7706 and clinical factors showed that expression levels of miRNA-299 and miRNA-7706 were significantly correlated with pathological stages and lymph node metastasis. ROC curve analysis showed that the areas under the curve were 0.837 and 0.845 for miRNA-299 and miRNA-7706 in the prediction of HCC, respectively. Survival analysis showed that the 5-year overall survival rate of patients with high expression levels of miRNA-299 and miRNA-7706 was significantly different from that of patients with low expression levels (P=0.016). Compared with cells transfected with scramble mimics, proliferation and invasion abilities of SK-HEP-1 cells transfected with miR-299 mimics and miRNA-7706 were significantly weakened. Results suggested that downregulation of miRNA-299 and miRNA-7706 can inhibit the proliferation of HCC cells and can be used as a new target for the treatment of HCC. D.A. Spandidos 2018-07 2018-05-16 /pmc/articles/PMC6019942/ /pubmed/29963149 http://dx.doi.org/10.3892/ol.2018.8710 Text en Copyright: © Wang 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 Wang, Fenglin Dai, Min Chen, Hongjie Li, Yue Zhang, Jiongshan Zou, Zengcheng Yang, Hongzhi Prognostic value of hsa-mir-299 and hsa-mir-7706 in hepatocellular carcinoma |
title | Prognostic value of hsa-mir-299 and hsa-mir-7706 in hepatocellular carcinoma |
title_full | Prognostic value of hsa-mir-299 and hsa-mir-7706 in hepatocellular carcinoma |
title_fullStr | Prognostic value of hsa-mir-299 and hsa-mir-7706 in hepatocellular carcinoma |
title_full_unstemmed | Prognostic value of hsa-mir-299 and hsa-mir-7706 in hepatocellular carcinoma |
title_short | Prognostic value of hsa-mir-299 and hsa-mir-7706 in hepatocellular carcinoma |
title_sort | prognostic value of hsa-mir-299 and hsa-mir-7706 in hepatocellular carcinoma |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6019942/ https://www.ncbi.nlm.nih.gov/pubmed/29963149 http://dx.doi.org/10.3892/ol.2018.8710 |
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