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Hinokiflavone induces apoptosis and inhibits migration of breast cancer cells via EMT signalling pathway

Hinokiflavone is a natural product, isolated from Selaginella P. Beauv, Juniperus phoenicea and Rhus succedanea. Even though hinokiflavone was reported to possess cytotoxicity to many cancer cells, and has potential in cancer treatment, the anti‐proliferation and anti‐metastasis efficacy of hinokifl...

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Autores principales: Huang, Wenzhen, Liu, Chi, Liu, Fengen, Liu, Zhiyong, Lai, Guie, Yi, Jian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7318630/
https://www.ncbi.nlm.nih.gov/pubmed/32107809
http://dx.doi.org/10.1002/cbf.3443
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author Huang, Wenzhen
Liu, Chi
Liu, Fengen
Liu, Zhiyong
Lai, Guie
Yi, Jian
author_facet Huang, Wenzhen
Liu, Chi
Liu, Fengen
Liu, Zhiyong
Lai, Guie
Yi, Jian
author_sort Huang, Wenzhen
collection PubMed
description Hinokiflavone is a natural product, isolated from Selaginella P. Beauv, Juniperus phoenicea and Rhus succedanea. Even though hinokiflavone was reported to possess cytotoxicity to many cancer cells, and has potential in cancer treatment, the anti‐proliferation and anti‐metastasis efficacy of hinokiflavone on human breast cancer cells has not a further research. In this study, we investigated the anti‐cancer activity of hinokiflavone in human breast cancer cells in vitro and in vivo. Hinokiflavone exhibited a time‐ and dose‐dependent manner apoptosis induction by upregulating expression of Bax and downregulating Bcl‐2 in breast cancer cells. Furthermore, hinokiflavone significantly inhibited the migration and invasion of breast cancer cells by impairing the process of epithelial‐to‐mesenchymal transition. In addition, the tumour growth was distinctly inhibited by treatment of hinokiflavone in a xenograft tumour mouse model of MDA‐MB‐231 cells. Immunohistochemical analysis of tumour sections showed that MMP‐2(+) cells and Ki‐67(+) cells were remarkably decreased in tumour tissues of mice after treatment of hinokiflavone, indicating that hinokiflavone inhibits not only proliferation but also metastasis of breast cancer cells. Our study suggested that hinokiflavone can be a potential drug to breast cancer. SIGNIFICANCE OF THE STUDY: Hinokiflavone significantly inhibited proliferation and induced apoptosis in breast cancer cells. In addition, hinokiflavone remarkably inhibited migration and invasion of breast cancer cells via EMT signalling pathway. It is worth noting that hinokiflavone possesses anti‐tumour effect in tumour mouse xenograft model of breast cancer. Overall, our results indicated that hinokiflavone may be a potential anticancer drug for breast cancer treatment.
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spelling pubmed-73186302020-06-29 Hinokiflavone induces apoptosis and inhibits migration of breast cancer cells via EMT signalling pathway Huang, Wenzhen Liu, Chi Liu, Fengen Liu, Zhiyong Lai, Guie Yi, Jian Cell Biochem Funct Research Articles Hinokiflavone is a natural product, isolated from Selaginella P. Beauv, Juniperus phoenicea and Rhus succedanea. Even though hinokiflavone was reported to possess cytotoxicity to many cancer cells, and has potential in cancer treatment, the anti‐proliferation and anti‐metastasis efficacy of hinokiflavone on human breast cancer cells has not a further research. In this study, we investigated the anti‐cancer activity of hinokiflavone in human breast cancer cells in vitro and in vivo. Hinokiflavone exhibited a time‐ and dose‐dependent manner apoptosis induction by upregulating expression of Bax and downregulating Bcl‐2 in breast cancer cells. Furthermore, hinokiflavone significantly inhibited the migration and invasion of breast cancer cells by impairing the process of epithelial‐to‐mesenchymal transition. In addition, the tumour growth was distinctly inhibited by treatment of hinokiflavone in a xenograft tumour mouse model of MDA‐MB‐231 cells. Immunohistochemical analysis of tumour sections showed that MMP‐2(+) cells and Ki‐67(+) cells were remarkably decreased in tumour tissues of mice after treatment of hinokiflavone, indicating that hinokiflavone inhibits not only proliferation but also metastasis of breast cancer cells. Our study suggested that hinokiflavone can be a potential drug to breast cancer. SIGNIFICANCE OF THE STUDY: Hinokiflavone significantly inhibited proliferation and induced apoptosis in breast cancer cells. In addition, hinokiflavone remarkably inhibited migration and invasion of breast cancer cells via EMT signalling pathway. It is worth noting that hinokiflavone possesses anti‐tumour effect in tumour mouse xenograft model of breast cancer. Overall, our results indicated that hinokiflavone may be a potential anticancer drug for breast cancer treatment. John Wiley and Sons Inc. 2020-02-27 2020-04 /pmc/articles/PMC7318630/ /pubmed/32107809 http://dx.doi.org/10.1002/cbf.3443 Text en © 2020 The Authors. Cell Biochemistry and Function published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Huang, Wenzhen
Liu, Chi
Liu, Fengen
Liu, Zhiyong
Lai, Guie
Yi, Jian
Hinokiflavone induces apoptosis and inhibits migration of breast cancer cells via EMT signalling pathway
title Hinokiflavone induces apoptosis and inhibits migration of breast cancer cells via EMT signalling pathway
title_full Hinokiflavone induces apoptosis and inhibits migration of breast cancer cells via EMT signalling pathway
title_fullStr Hinokiflavone induces apoptosis and inhibits migration of breast cancer cells via EMT signalling pathway
title_full_unstemmed Hinokiflavone induces apoptosis and inhibits migration of breast cancer cells via EMT signalling pathway
title_short Hinokiflavone induces apoptosis and inhibits migration of breast cancer cells via EMT signalling pathway
title_sort hinokiflavone induces apoptosis and inhibits migration of breast cancer cells via emt signalling pathway
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7318630/
https://www.ncbi.nlm.nih.gov/pubmed/32107809
http://dx.doi.org/10.1002/cbf.3443
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