Let-7b contributes to hepatocellular cancer progression through Wnt/β-catenin signaling
Elevated evidences show that microRNAs (miRNAs) play vital roles in tumor progression regulation. However, the functional role of let-7b in hepatocellular carcinoma (HCC) is still largely unknown. In this study, we try to investigate the biological activity of let-7b in human HCC cells and try to fi...
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doaj-92afc9a1158144c297a3f527dcd2fc5a2020-11-24T23:15:15ZengElsevierSaudi Journal of Biological Sciences1319-562X2018-07-01255953958Let-7b contributes to hepatocellular cancer progression through Wnt/β-catenin signalingYiwei Wang0Yanbo Mo1Lin Wang2Peng Su3Yuxi Xie4North China University of Science and Technology Affiliated Hospital, Tangshan 063000, PR ChinaNorth China University of Science and Technology Affiliated Hospital, Tangshan 063000, PR ChinaNorth China University of Science and Technology Affiliated Hospital, Tangshan 063000, PR ChinaNorth China University of Technology, Tangshan 063000, PR ChinaNorth China University of Science and Technology Affiliated Hospital, Tangshan 063000, PR China; Corresponding author.Elevated evidences show that microRNAs (miRNAs) play vital roles in tumor progression regulation. However, the functional role of let-7b in hepatocellular carcinoma (HCC) is still largely unknown. In this study, we try to investigate the biological activity of let-7b in human HCC cells and try to find the potential regulatory signaling pathway. Our results indicate that let- 7b was remarkably down-regulated in human HCC tissues by qRT-PCR. In addition, let-7b overexpression decreased the expression of β-catenin and c-Myc, while upregulated E-cadherin expression in HCC cells which was verified by quantitative real-time PCR (qRT-PCR) and western blotting. Furthermore, Wnt/β-catenin was involved in let-7b biological activity which was revealed by luciferase assay. Moreover, Wnt/β-catenin signaling inhibitor blocks HCC cell proliferation which is as the same pattern as let-7b overexpression inhibits in HCC cells proliferation. In conclusion, down-regulated let-7b promotes HCC cell proliferation through Wnt/β-catenin signaling in HCC cells. These results suggested that appropriate manipulation of let-7b might be a new treatment of human HCC in the future. Keywords: Let-7b, Wnt/β-catenin signaling, Cell proliferationhttp://www.sciencedirect.com/science/article/pii/S1319562X18300731 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Yiwei Wang Yanbo Mo Lin Wang Peng Su Yuxi Xie |
spellingShingle |
Yiwei Wang Yanbo Mo Lin Wang Peng Su Yuxi Xie Let-7b contributes to hepatocellular cancer progression through Wnt/β-catenin signaling Saudi Journal of Biological Sciences |
author_facet |
Yiwei Wang Yanbo Mo Lin Wang Peng Su Yuxi Xie |
author_sort |
Yiwei Wang |
title |
Let-7b contributes to hepatocellular cancer progression through Wnt/β-catenin signaling |
title_short |
Let-7b contributes to hepatocellular cancer progression through Wnt/β-catenin signaling |
title_full |
Let-7b contributes to hepatocellular cancer progression through Wnt/β-catenin signaling |
title_fullStr |
Let-7b contributes to hepatocellular cancer progression through Wnt/β-catenin signaling |
title_full_unstemmed |
Let-7b contributes to hepatocellular cancer progression through Wnt/β-catenin signaling |
title_sort |
let-7b contributes to hepatocellular cancer progression through wnt/β-catenin signaling |
publisher |
Elsevier |
series |
Saudi Journal of Biological Sciences |
issn |
1319-562X |
publishDate |
2018-07-01 |
description |
Elevated evidences show that microRNAs (miRNAs) play vital roles in tumor progression regulation. However, the functional role of let-7b in hepatocellular carcinoma (HCC) is still largely unknown. In this study, we try to investigate the biological activity of let-7b in human HCC cells and try to find the potential regulatory signaling pathway. Our results indicate that let- 7b was remarkably down-regulated in human HCC tissues by qRT-PCR. In addition, let-7b overexpression decreased the expression of β-catenin and c-Myc, while upregulated E-cadherin expression in HCC cells which was verified by quantitative real-time PCR (qRT-PCR) and western blotting. Furthermore, Wnt/β-catenin was involved in let-7b biological activity which was revealed by luciferase assay. Moreover, Wnt/β-catenin signaling inhibitor blocks HCC cell proliferation which is as the same pattern as let-7b overexpression inhibits in HCC cells proliferation. In conclusion, down-regulated let-7b promotes HCC cell proliferation through Wnt/β-catenin signaling in HCC cells. These results suggested that appropriate manipulation of let-7b might be a new treatment of human HCC in the future. Keywords: Let-7b, Wnt/β-catenin signaling, Cell proliferation |
url |
http://www.sciencedirect.com/science/article/pii/S1319562X18300731 |
work_keys_str_mv |
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