Cargando…

All-trans retinoic acids induce differentiation and sensitize a radioresistant breast cancer cells to chemotherapy

BACKGROUND: Radiotherapy is of critical importance in the treatment of breast cancer. However, not all patients derive therapeutic benefit and some breast cancers are resistant to the treatment, and are thus evidenced with prospective distant metastatic spread and local recurrence. In this study, we...

Descripción completa

Detalles Bibliográficos
Autores principales: Yan, Yunwen, Li, Zhen, Xu, Xiang, Chen, Clark, Wei, Wei, Fan, Ming, Chen, Xufeng, Li, Jian Jian, Wang, Yuan, Huang, Jiaoti
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4815257/
https://www.ncbi.nlm.nih.gov/pubmed/27036550
http://dx.doi.org/10.1186/s12906-016-1088-y
_version_ 1782424570321436672
author Yan, Yunwen
Li, Zhen
Xu, Xiang
Chen, Clark
Wei, Wei
Fan, Ming
Chen, Xufeng
Li, Jian Jian
Wang, Yuan
Huang, Jiaoti
author_facet Yan, Yunwen
Li, Zhen
Xu, Xiang
Chen, Clark
Wei, Wei
Fan, Ming
Chen, Xufeng
Li, Jian Jian
Wang, Yuan
Huang, Jiaoti
author_sort Yan, Yunwen
collection PubMed
description BACKGROUND: Radiotherapy is of critical importance in the treatment of breast cancer. However, not all patients derive therapeutic benefit and some breast cancers are resistant to the treatment, and are thus evidenced with prospective distant metastatic spread and local recurrence. In this study, we investigated the potential therapeutic effects of all-trans retinoic acid (ATRA) on radiation-resistant breast cancer cells and the associated invasiveness. METHODS: The MCF7/C6 cells with gained radiation resistance after a long term treatment with fractionated ionizing radiation were derived from human breast cancer MCF7 cell line, and are enriched with cells expressing putative breast cancer stem cell biomarker CD44(+)/CD24(-/low)/ALDH(+). The enhanced invasiveness and the acquired resistances to chemotherapeutic treatments of MCF7/C6 cells were measured, and potential effects of all-trans retinoic acid (ATRA) on the induction of differentiation, invasion and migration, and on the sensitivities to chemotherapies in MCF7/C6 cells were investigated. RESULTS: MCF7/C6 cells are with enrichment of cancer stem-cell like cells with positive staining of CD44(+)/CD24(-/low), OCT3/4 and NANOG. MCF7/C6 cells showed an increased tumoregensis potential and enhanced aggressiveness of invasion and migration. Treatment with ATRA induces the differentiation in MCF7/C6 cells, resulting in reduced invasiveness and migration, and increased sensitivity to Epirubincin treatment. CONCLUSION: Our study suggests a potential clinic impact for ATRA as a chemotherapeutic agent for treatment of therapy-resistant breast cancer especially for the metastatic lesions. The study also provides a rationale for ATRA as a sensitizer of Epirubincin, a first-line treatment option for breast cancer patients. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12906-016-1088-y) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-4815257
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-48152572016-04-01 All-trans retinoic acids induce differentiation and sensitize a radioresistant breast cancer cells to chemotherapy Yan, Yunwen Li, Zhen Xu, Xiang Chen, Clark Wei, Wei Fan, Ming Chen, Xufeng Li, Jian Jian Wang, Yuan Huang, Jiaoti BMC Complement Altern Med Research Article BACKGROUND: Radiotherapy is of critical importance in the treatment of breast cancer. However, not all patients derive therapeutic benefit and some breast cancers are resistant to the treatment, and are thus evidenced with prospective distant metastatic spread and local recurrence. In this study, we investigated the potential therapeutic effects of all-trans retinoic acid (ATRA) on radiation-resistant breast cancer cells and the associated invasiveness. METHODS: The MCF7/C6 cells with gained radiation resistance after a long term treatment with fractionated ionizing radiation were derived from human breast cancer MCF7 cell line, and are enriched with cells expressing putative breast cancer stem cell biomarker CD44(+)/CD24(-/low)/ALDH(+). The enhanced invasiveness and the acquired resistances to chemotherapeutic treatments of MCF7/C6 cells were measured, and potential effects of all-trans retinoic acid (ATRA) on the induction of differentiation, invasion and migration, and on the sensitivities to chemotherapies in MCF7/C6 cells were investigated. RESULTS: MCF7/C6 cells are with enrichment of cancer stem-cell like cells with positive staining of CD44(+)/CD24(-/low), OCT3/4 and NANOG. MCF7/C6 cells showed an increased tumoregensis potential and enhanced aggressiveness of invasion and migration. Treatment with ATRA induces the differentiation in MCF7/C6 cells, resulting in reduced invasiveness and migration, and increased sensitivity to Epirubincin treatment. CONCLUSION: Our study suggests a potential clinic impact for ATRA as a chemotherapeutic agent for treatment of therapy-resistant breast cancer especially for the metastatic lesions. The study also provides a rationale for ATRA as a sensitizer of Epirubincin, a first-line treatment option for breast cancer patients. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12906-016-1088-y) contains supplementary material, which is available to authorized users. BioMed Central 2016-03-31 /pmc/articles/PMC4815257/ /pubmed/27036550 http://dx.doi.org/10.1186/s12906-016-1088-y Text en © Yan et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Yan, Yunwen
Li, Zhen
Xu, Xiang
Chen, Clark
Wei, Wei
Fan, Ming
Chen, Xufeng
Li, Jian Jian
Wang, Yuan
Huang, Jiaoti
All-trans retinoic acids induce differentiation and sensitize a radioresistant breast cancer cells to chemotherapy
title All-trans retinoic acids induce differentiation and sensitize a radioresistant breast cancer cells to chemotherapy
title_full All-trans retinoic acids induce differentiation and sensitize a radioresistant breast cancer cells to chemotherapy
title_fullStr All-trans retinoic acids induce differentiation and sensitize a radioresistant breast cancer cells to chemotherapy
title_full_unstemmed All-trans retinoic acids induce differentiation and sensitize a radioresistant breast cancer cells to chemotherapy
title_short All-trans retinoic acids induce differentiation and sensitize a radioresistant breast cancer cells to chemotherapy
title_sort all-trans retinoic acids induce differentiation and sensitize a radioresistant breast cancer cells to chemotherapy
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4815257/
https://www.ncbi.nlm.nih.gov/pubmed/27036550
http://dx.doi.org/10.1186/s12906-016-1088-y
work_keys_str_mv AT yanyunwen alltransretinoicacidsinducedifferentiationandsensitizearadioresistantbreastcancercellstochemotherapy
AT lizhen alltransretinoicacidsinducedifferentiationandsensitizearadioresistantbreastcancercellstochemotherapy
AT xuxiang alltransretinoicacidsinducedifferentiationandsensitizearadioresistantbreastcancercellstochemotherapy
AT chenclark alltransretinoicacidsinducedifferentiationandsensitizearadioresistantbreastcancercellstochemotherapy
AT weiwei alltransretinoicacidsinducedifferentiationandsensitizearadioresistantbreastcancercellstochemotherapy
AT fanming alltransretinoicacidsinducedifferentiationandsensitizearadioresistantbreastcancercellstochemotherapy
AT chenxufeng alltransretinoicacidsinducedifferentiationandsensitizearadioresistantbreastcancercellstochemotherapy
AT lijianjian alltransretinoicacidsinducedifferentiationandsensitizearadioresistantbreastcancercellstochemotherapy
AT wangyuan alltransretinoicacidsinducedifferentiationandsensitizearadioresistantbreastcancercellstochemotherapy
AT huangjiaoti alltransretinoicacidsinducedifferentiationandsensitizearadioresistantbreastcancercellstochemotherapy