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c-MET Protects Breast Cancer Cells from Apoptosis Induced by Sodium Butyrate

Sodium Butyrate (NaBu) is regarded as a potential reagent for cancer therapy. In this study, a specific breast cancer cell population that is resistant NaBu treatment was identified. These cells possess cancer stem cell characters, such as the capability of sphere formation in vitro and high tumor i...

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Detalles Bibliográficos
Autores principales: Sun, Bo, Liu, Rui, Xiao, Zhong-Dang, Zhu, Xuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3257283/
https://www.ncbi.nlm.nih.gov/pubmed/22253909
http://dx.doi.org/10.1371/journal.pone.0030143
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author Sun, Bo
Liu, Rui
Xiao, Zhong-Dang
Zhu, Xuan
author_facet Sun, Bo
Liu, Rui
Xiao, Zhong-Dang
Zhu, Xuan
author_sort Sun, Bo
collection PubMed
description Sodium Butyrate (NaBu) is regarded as a potential reagent for cancer therapy. In this study, a specific breast cancer cell population that is resistant NaBu treatment was identified. These cells possess cancer stem cell characters, such as the capability of sphere formation in vitro and high tumor incident rate (85%) in mouse model. Forty percent of the NaBu resistant cells express the cancer stem cells marker, the CD133, whereas only 10% intact cells present the CD133 antigen. Furthermore, the endogenous expressing c-MET contributes to the survival of cancer stem cell population from the treatment of NaBu. The CD133+ group also presents a higher level of c-MET. A combination treatment of MET siRNA and NaBu efficiently prohibited the breast cancer progression, and the incident rate of the tumor decrease to 18%. This study may help to develop a new and alternative strategy for breast cancer therapy.
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spelling pubmed-32572832012-01-17 c-MET Protects Breast Cancer Cells from Apoptosis Induced by Sodium Butyrate Sun, Bo Liu, Rui Xiao, Zhong-Dang Zhu, Xuan PLoS One Research Article Sodium Butyrate (NaBu) is regarded as a potential reagent for cancer therapy. In this study, a specific breast cancer cell population that is resistant NaBu treatment was identified. These cells possess cancer stem cell characters, such as the capability of sphere formation in vitro and high tumor incident rate (85%) in mouse model. Forty percent of the NaBu resistant cells express the cancer stem cells marker, the CD133, whereas only 10% intact cells present the CD133 antigen. Furthermore, the endogenous expressing c-MET contributes to the survival of cancer stem cell population from the treatment of NaBu. The CD133+ group also presents a higher level of c-MET. A combination treatment of MET siRNA and NaBu efficiently prohibited the breast cancer progression, and the incident rate of the tumor decrease to 18%. This study may help to develop a new and alternative strategy for breast cancer therapy. Public Library of Science 2012-01-12 /pmc/articles/PMC3257283/ /pubmed/22253909 http://dx.doi.org/10.1371/journal.pone.0030143 Text en Sun et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Sun, Bo
Liu, Rui
Xiao, Zhong-Dang
Zhu, Xuan
c-MET Protects Breast Cancer Cells from Apoptosis Induced by Sodium Butyrate
title c-MET Protects Breast Cancer Cells from Apoptosis Induced by Sodium Butyrate
title_full c-MET Protects Breast Cancer Cells from Apoptosis Induced by Sodium Butyrate
title_fullStr c-MET Protects Breast Cancer Cells from Apoptosis Induced by Sodium Butyrate
title_full_unstemmed c-MET Protects Breast Cancer Cells from Apoptosis Induced by Sodium Butyrate
title_short c-MET Protects Breast Cancer Cells from Apoptosis Induced by Sodium Butyrate
title_sort c-met protects breast cancer cells from apoptosis induced by sodium butyrate
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3257283/
https://www.ncbi.nlm.nih.gov/pubmed/22253909
http://dx.doi.org/10.1371/journal.pone.0030143
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