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Bufalin suppresses hepatocarcinogenesis by targeting β-catenin/TCF signaling via cell cycle-related kinase

Hepatocellular carcinoma (HCC) is one of the most aggressive malignant tumors, of which treatment options are limited especially in advanced stage. Bufalin, the major digoxin-like component of the traditional Chinese medicine Chansu, exhibits significant antitumor activities in hepatoma cells, but t...

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Autores principales: Yu, Zhuo, Feng, Hai, Sun, Xuehua, Zhuo, Yunhui, Li, Man, Zhou, Zhenhua, Huang, Lingying, Jiang, Yun, Zhu, Xiaojun, Zhang, Xin, Le, Fan, Zheng, Chao, Cheng, Alfred Szelok, Gao, Yueqiu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5832857/
https://www.ncbi.nlm.nih.gov/pubmed/29497076
http://dx.doi.org/10.1038/s41598-018-22113-2
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author Yu, Zhuo
Feng, Hai
Sun, Xuehua
Zhuo, Yunhui
Li, Man
Zhou, Zhenhua
Huang, Lingying
Jiang, Yun
Zhu, Xiaojun
Zhang, Xin
Le, Fan
Zheng, Chao
Cheng, Alfred Szelok
Gao, Yueqiu
author_facet Yu, Zhuo
Feng, Hai
Sun, Xuehua
Zhuo, Yunhui
Li, Man
Zhou, Zhenhua
Huang, Lingying
Jiang, Yun
Zhu, Xiaojun
Zhang, Xin
Le, Fan
Zheng, Chao
Cheng, Alfred Szelok
Gao, Yueqiu
author_sort Yu, Zhuo
collection PubMed
description Hepatocellular carcinoma (HCC) is one of the most aggressive malignant tumors, of which treatment options are limited especially in advanced stage. Bufalin, the major digoxin-like component of the traditional Chinese medicine Chansu, exhibits significant antitumor activities in hepatoma cells, but the potential mechanism is obscure. Cell cycle-related kinase (CCRK) is recently identified to be a crucial oncogenic master regulator to drive hepatocarcinogenesis. Here we investigated the molecular function of bufalin on CCRK-regulated signaling pathway, and expounded the underlying mechanism in HCC suppression. In vitro with PLC5 HCC cells and human immortal LO2 cells, proliferation, malignant transformation and cell cycle progression assays were performed to evaluate the antitumor effect of bufalin. In vivo with xenograft and orthotopic mice models, tumor growths with weight and volume change were assessed with or without bufalin treatment. Western blot, RT-qPCR, immunofluorescence and immunohistochemistry were conducted to examine the expression level of CCRK and β-catenin/TCF signaling cascade. We revealed that bufalin suppresses PLC5 HCC cell proliferation, transformation and cell cycle progression rather than LO2 cells, which is correlated with CCRK-mediated β-catenin/TCF signaling. It was also confirmed in mice model. Thus, bufalin is a potential anti-HCC therapeutic candidate through the inhibition of CCRK-driven β-catenin/TCF oncogenic signaling pathway.
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spelling pubmed-58328572018-03-05 Bufalin suppresses hepatocarcinogenesis by targeting β-catenin/TCF signaling via cell cycle-related kinase Yu, Zhuo Feng, Hai Sun, Xuehua Zhuo, Yunhui Li, Man Zhou, Zhenhua Huang, Lingying Jiang, Yun Zhu, Xiaojun Zhang, Xin Le, Fan Zheng, Chao Cheng, Alfred Szelok Gao, Yueqiu Sci Rep Article Hepatocellular carcinoma (HCC) is one of the most aggressive malignant tumors, of which treatment options are limited especially in advanced stage. Bufalin, the major digoxin-like component of the traditional Chinese medicine Chansu, exhibits significant antitumor activities in hepatoma cells, but the potential mechanism is obscure. Cell cycle-related kinase (CCRK) is recently identified to be a crucial oncogenic master regulator to drive hepatocarcinogenesis. Here we investigated the molecular function of bufalin on CCRK-regulated signaling pathway, and expounded the underlying mechanism in HCC suppression. In vitro with PLC5 HCC cells and human immortal LO2 cells, proliferation, malignant transformation and cell cycle progression assays were performed to evaluate the antitumor effect of bufalin. In vivo with xenograft and orthotopic mice models, tumor growths with weight and volume change were assessed with or without bufalin treatment. Western blot, RT-qPCR, immunofluorescence and immunohistochemistry were conducted to examine the expression level of CCRK and β-catenin/TCF signaling cascade. We revealed that bufalin suppresses PLC5 HCC cell proliferation, transformation and cell cycle progression rather than LO2 cells, which is correlated with CCRK-mediated β-catenin/TCF signaling. It was also confirmed in mice model. Thus, bufalin is a potential anti-HCC therapeutic candidate through the inhibition of CCRK-driven β-catenin/TCF oncogenic signaling pathway. Nature Publishing Group UK 2018-03-01 /pmc/articles/PMC5832857/ /pubmed/29497076 http://dx.doi.org/10.1038/s41598-018-22113-2 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Yu, Zhuo
Feng, Hai
Sun, Xuehua
Zhuo, Yunhui
Li, Man
Zhou, Zhenhua
Huang, Lingying
Jiang, Yun
Zhu, Xiaojun
Zhang, Xin
Le, Fan
Zheng, Chao
Cheng, Alfred Szelok
Gao, Yueqiu
Bufalin suppresses hepatocarcinogenesis by targeting β-catenin/TCF signaling via cell cycle-related kinase
title Bufalin suppresses hepatocarcinogenesis by targeting β-catenin/TCF signaling via cell cycle-related kinase
title_full Bufalin suppresses hepatocarcinogenesis by targeting β-catenin/TCF signaling via cell cycle-related kinase
title_fullStr Bufalin suppresses hepatocarcinogenesis by targeting β-catenin/TCF signaling via cell cycle-related kinase
title_full_unstemmed Bufalin suppresses hepatocarcinogenesis by targeting β-catenin/TCF signaling via cell cycle-related kinase
title_short Bufalin suppresses hepatocarcinogenesis by targeting β-catenin/TCF signaling via cell cycle-related kinase
title_sort bufalin suppresses hepatocarcinogenesis by targeting β-catenin/tcf signaling via cell cycle-related kinase
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5832857/
https://www.ncbi.nlm.nih.gov/pubmed/29497076
http://dx.doi.org/10.1038/s41598-018-22113-2
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