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Gomisin M2 from Baizuan suppresses breast cancer stem cell proliferation in a zebrafish xenograft model
Gomisin M2 isolated from Schisandra viridis A. C. Smith has potential anti-tumor effects on certain cancers, including breast cancer. However, only a few investigations have been conducted on the effects of Gomisin M2 on breast cancer stem cells (CSCs), which have the ability to self-renew and diffe...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6814583/ https://www.ncbi.nlm.nih.gov/pubmed/31612865 http://dx.doi.org/10.18632/aging.102323 |
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author | Yang, Yeguo Hao, Erwei Pan, Xianglong Tan, Dechao Du, Zhengcai Xie, Jinling Hou, Xiaotao Deng, Jiagang Wei, Kun |
author_facet | Yang, Yeguo Hao, Erwei Pan, Xianglong Tan, Dechao Du, Zhengcai Xie, Jinling Hou, Xiaotao Deng, Jiagang Wei, Kun |
author_sort | Yang, Yeguo |
collection | PubMed |
description | Gomisin M2 isolated from Schisandra viridis A. C. Smith has potential anti-tumor effects on certain cancers, including breast cancer. However, only a few investigations have been conducted on the effects of Gomisin M2 on breast cancer stem cells (CSCs), which have the ability to self-renew and differentiate, as a possible strategy to resolve cancer cell resistance to apoptosis and to improve treatments. It is essential to investigate the effects of Gomisin M2 on breast cancer stem cells (BCSCs). In this study, we enriched breast cancer stem cells with CD44+/CD24- from MDA-MB-231 and HCC1806 cells through magnetic-activated cell sorting and cultured these in serum-free medium. The ability of Gomisin M2 to kill breast cancer stem cells was evaluated in vitro and in vivo. Gomisin M2 significantly inhibited the proliferation of the triple-negative breast cancer cell lines and mammosphere formation in breast CSCs and downregulated the Wnt/β-catenin self-renewal pathway. Moreover, Gomisin M2 induced apoptosis and blocked the mitochondrial membrane potential of BCSCs. Gomisin M2 suppressed the proliferation of MDA-MB-231 and HCC1806 xenografts in zebrafish. Together, these findings suggest that the anti-BCSC activity of Gomisin M2 could become a promising starting point for the discovery of novel BCSC-targeting drugs. |
format | Online Article Text |
id | pubmed-6814583 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Impact Journals |
record_format | MEDLINE/PubMed |
spelling | pubmed-68145832019-11-05 Gomisin M2 from Baizuan suppresses breast cancer stem cell proliferation in a zebrafish xenograft model Yang, Yeguo Hao, Erwei Pan, Xianglong Tan, Dechao Du, Zhengcai Xie, Jinling Hou, Xiaotao Deng, Jiagang Wei, Kun Aging (Albany NY) Research Paper Gomisin M2 isolated from Schisandra viridis A. C. Smith has potential anti-tumor effects on certain cancers, including breast cancer. However, only a few investigations have been conducted on the effects of Gomisin M2 on breast cancer stem cells (CSCs), which have the ability to self-renew and differentiate, as a possible strategy to resolve cancer cell resistance to apoptosis and to improve treatments. It is essential to investigate the effects of Gomisin M2 on breast cancer stem cells (BCSCs). In this study, we enriched breast cancer stem cells with CD44+/CD24- from MDA-MB-231 and HCC1806 cells through magnetic-activated cell sorting and cultured these in serum-free medium. The ability of Gomisin M2 to kill breast cancer stem cells was evaluated in vitro and in vivo. Gomisin M2 significantly inhibited the proliferation of the triple-negative breast cancer cell lines and mammosphere formation in breast CSCs and downregulated the Wnt/β-catenin self-renewal pathway. Moreover, Gomisin M2 induced apoptosis and blocked the mitochondrial membrane potential of BCSCs. Gomisin M2 suppressed the proliferation of MDA-MB-231 and HCC1806 xenografts in zebrafish. Together, these findings suggest that the anti-BCSC activity of Gomisin M2 could become a promising starting point for the discovery of novel BCSC-targeting drugs. Impact Journals 2019-10-14 /pmc/articles/PMC6814583/ /pubmed/31612865 http://dx.doi.org/10.18632/aging.102323 Text en Copyright © 2019 Yang et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Yang, Yeguo Hao, Erwei Pan, Xianglong Tan, Dechao Du, Zhengcai Xie, Jinling Hou, Xiaotao Deng, Jiagang Wei, Kun Gomisin M2 from Baizuan suppresses breast cancer stem cell proliferation in a zebrafish xenograft model |
title | Gomisin M2 from Baizuan suppresses breast cancer stem cell proliferation in a zebrafish xenograft model |
title_full | Gomisin M2 from Baizuan suppresses breast cancer stem cell proliferation in a zebrafish xenograft model |
title_fullStr | Gomisin M2 from Baizuan suppresses breast cancer stem cell proliferation in a zebrafish xenograft model |
title_full_unstemmed | Gomisin M2 from Baizuan suppresses breast cancer stem cell proliferation in a zebrafish xenograft model |
title_short | Gomisin M2 from Baizuan suppresses breast cancer stem cell proliferation in a zebrafish xenograft model |
title_sort | gomisin m2 from baizuan suppresses breast cancer stem cell proliferation in a zebrafish xenograft model |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6814583/ https://www.ncbi.nlm.nih.gov/pubmed/31612865 http://dx.doi.org/10.18632/aging.102323 |
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