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Isolation and characterization of adult mammary stem cells from breast cancer-adjacent tissues

Normal adult mammary stem cells (AMSCs) are promising sources for breast reconstruction, particularly following the resection of breast tumors. However, carcinogenic events can potentially convert normal AMSCs to cancer stem cells, posing a safety concern for the use of AMSCs for clinical tissue reg...

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Autores principales: Shi, Ai-Ping, Fan, Zhi-Min, Ma, Ke-Wei, Jiang, Yan-Fang, Wang, Lei, Zhang, Ke-Wei, Fu, Shi-Bo, Xu, Ning, Zhang, Zhi-Ru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5588124/
https://www.ncbi.nlm.nih.gov/pubmed/28927044
http://dx.doi.org/10.3892/ol.2017.6485
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author Shi, Ai-Ping
Fan, Zhi-Min
Ma, Ke-Wei
Jiang, Yan-Fang
Wang, Lei
Zhang, Ke-Wei
Fu, Shi-Bo
Xu, Ning
Zhang, Zhi-Ru
author_facet Shi, Ai-Ping
Fan, Zhi-Min
Ma, Ke-Wei
Jiang, Yan-Fang
Wang, Lei
Zhang, Ke-Wei
Fu, Shi-Bo
Xu, Ning
Zhang, Zhi-Ru
author_sort Shi, Ai-Ping
collection PubMed
description Normal adult mammary stem cells (AMSCs) are promising sources for breast reconstruction, particularly following the resection of breast tumors. However, carcinogenic events can potentially convert normal AMSCs to cancer stem cells, posing a safety concern for the use of AMSCs for clinical tissue regeneration. In the present study, AMSCs and autologous primary breast cancer cells were isolated and compared for their ability to differentiate, their gene expression profile, and their potential to form tumors in vivo. AMSCs were isolated from normal tissue surrounding primary breast tumors by immunomagnetic sorting. The pluripotency of these cells was investigated by differentiation analysis, and gene expression profiles were compared with microarrays. Differentially expressed candidate genes were confirmed by reverse transcription-polymerase chain reaction and western blot analyses. The in vivo tumorigenicity of these cells, compared with low-malignancy MCF-7 cells, was also investigated by xenograft tumor formation analysis. The results revealed that AMSCs isolated from normal tissues surrounding primary breast tumors were positive for the stem cell markers epithelial-specific antigen and keratin-19. When stimulated with basic fibroblast growth factor, a differentiation agent, these AMSCs formed lobuloalveolar structures with myoepithelia that were positive for common acute lymphoblastic leukemia antigen. The gene expression profiles revealed that, compared with cancer cells, AMSCs expressed low levels of oncogenes, including MYC, RAS and ErbB receptor tyrosine kinase 2, and high levels of tumor suppressor genes, including RB transcriptional corepressor 1, phosphatase and tensin homolog, and cyclin-dependent kinase inhibitor 2A. When injected into nude non-obese diabetic/severe combined immunodeficiency-type mice, the AMSCs did not form tumors, and regular mammary ductal structures were generated. The AMSCs isolated from normal tissue adjacent to primary breast tumors had the normal phenotype of mammary stem cells, and therefore may be promising candidates for mammary reconstruction subsequent to breast tumor resection.
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spelling pubmed-55881242017-09-18 Isolation and characterization of adult mammary stem cells from breast cancer-adjacent tissues Shi, Ai-Ping Fan, Zhi-Min Ma, Ke-Wei Jiang, Yan-Fang Wang, Lei Zhang, Ke-Wei Fu, Shi-Bo Xu, Ning Zhang, Zhi-Ru Oncol Lett Articles Normal adult mammary stem cells (AMSCs) are promising sources for breast reconstruction, particularly following the resection of breast tumors. However, carcinogenic events can potentially convert normal AMSCs to cancer stem cells, posing a safety concern for the use of AMSCs for clinical tissue regeneration. In the present study, AMSCs and autologous primary breast cancer cells were isolated and compared for their ability to differentiate, their gene expression profile, and their potential to form tumors in vivo. AMSCs were isolated from normal tissue surrounding primary breast tumors by immunomagnetic sorting. The pluripotency of these cells was investigated by differentiation analysis, and gene expression profiles were compared with microarrays. Differentially expressed candidate genes were confirmed by reverse transcription-polymerase chain reaction and western blot analyses. The in vivo tumorigenicity of these cells, compared with low-malignancy MCF-7 cells, was also investigated by xenograft tumor formation analysis. The results revealed that AMSCs isolated from normal tissues surrounding primary breast tumors were positive for the stem cell markers epithelial-specific antigen and keratin-19. When stimulated with basic fibroblast growth factor, a differentiation agent, these AMSCs formed lobuloalveolar structures with myoepithelia that were positive for common acute lymphoblastic leukemia antigen. The gene expression profiles revealed that, compared with cancer cells, AMSCs expressed low levels of oncogenes, including MYC, RAS and ErbB receptor tyrosine kinase 2, and high levels of tumor suppressor genes, including RB transcriptional corepressor 1, phosphatase and tensin homolog, and cyclin-dependent kinase inhibitor 2A. When injected into nude non-obese diabetic/severe combined immunodeficiency-type mice, the AMSCs did not form tumors, and regular mammary ductal structures were generated. The AMSCs isolated from normal tissue adjacent to primary breast tumors had the normal phenotype of mammary stem cells, and therefore may be promising candidates for mammary reconstruction subsequent to breast tumor resection. D.A. Spandidos 2017-09 2017-06-28 /pmc/articles/PMC5588124/ /pubmed/28927044 http://dx.doi.org/10.3892/ol.2017.6485 Text en Copyright: © Shi et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Shi, Ai-Ping
Fan, Zhi-Min
Ma, Ke-Wei
Jiang, Yan-Fang
Wang, Lei
Zhang, Ke-Wei
Fu, Shi-Bo
Xu, Ning
Zhang, Zhi-Ru
Isolation and characterization of adult mammary stem cells from breast cancer-adjacent tissues
title Isolation and characterization of adult mammary stem cells from breast cancer-adjacent tissues
title_full Isolation and characterization of adult mammary stem cells from breast cancer-adjacent tissues
title_fullStr Isolation and characterization of adult mammary stem cells from breast cancer-adjacent tissues
title_full_unstemmed Isolation and characterization of adult mammary stem cells from breast cancer-adjacent tissues
title_short Isolation and characterization of adult mammary stem cells from breast cancer-adjacent tissues
title_sort isolation and characterization of adult mammary stem cells from breast cancer-adjacent tissues
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5588124/
https://www.ncbi.nlm.nih.gov/pubmed/28927044
http://dx.doi.org/10.3892/ol.2017.6485
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