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EO771, is it a well‐characterized cell line for mouse mammary cancer model? Limit and uncertainty

Among mouse mammary tumor models, syngeneic cell lines present an advantage for the study of immune response. However, few of these models are well characterized. The tumor line EO771 is derived from spontaneous breast cancer of C57BL/6 mice. These cells are widely used but are referenced under diff...

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Autores principales: Le Naour, Augustin, Rossary, Adrien, Vasson, Marie‐Paule
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/PMC7643677/
https://www.ncbi.nlm.nih.gov/pubmed/33026171
http://dx.doi.org/10.1002/cam4.3295
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author Le Naour, Augustin
Rossary, Adrien
Vasson, Marie‐Paule
author_facet Le Naour, Augustin
Rossary, Adrien
Vasson, Marie‐Paule
author_sort Le Naour, Augustin
collection PubMed
description Among mouse mammary tumor models, syngeneic cell lines present an advantage for the study of immune response. However, few of these models are well characterized. The tumor line EO771 is derived from spontaneous breast cancer of C57BL/6 mice. These cells are widely used but are referenced under different names: EO771, EO 771, and E0771. The characteristics of the EO771 cells are well described but some data are contradictory. This cell line presents the great interest of developing an immunocompetent neoplastic model using an orthotopic implantation reflecting the mammary tumors encountered in breast cancer patients. This review presents the phenotype characteristics of EO771 and its sensitivity to nutrients and different therapies such as radiotherapy, chemotherapy, hormone therapy, and immunotherapy.
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spelling pubmed-76436772020-11-13 EO771, is it a well‐characterized cell line for mouse mammary cancer model? Limit and uncertainty Le Naour, Augustin Rossary, Adrien Vasson, Marie‐Paule Cancer Med Cancer Biology Among mouse mammary tumor models, syngeneic cell lines present an advantage for the study of immune response. However, few of these models are well characterized. The tumor line EO771 is derived from spontaneous breast cancer of C57BL/6 mice. These cells are widely used but are referenced under different names: EO771, EO 771, and E0771. The characteristics of the EO771 cells are well described but some data are contradictory. This cell line presents the great interest of developing an immunocompetent neoplastic model using an orthotopic implantation reflecting the mammary tumors encountered in breast cancer patients. This review presents the phenotype characteristics of EO771 and its sensitivity to nutrients and different therapies such as radiotherapy, chemotherapy, hormone therapy, and immunotherapy. John Wiley and Sons Inc. 2020-10-07 /pmc/articles/PMC7643677/ /pubmed/33026171 http://dx.doi.org/10.1002/cam4.3295 Text en © 2020 The Authors. Cancer Medicine 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 Cancer Biology
Le Naour, Augustin
Rossary, Adrien
Vasson, Marie‐Paule
EO771, is it a well‐characterized cell line for mouse mammary cancer model? Limit and uncertainty
title EO771, is it a well‐characterized cell line for mouse mammary cancer model? Limit and uncertainty
title_full EO771, is it a well‐characterized cell line for mouse mammary cancer model? Limit and uncertainty
title_fullStr EO771, is it a well‐characterized cell line for mouse mammary cancer model? Limit and uncertainty
title_full_unstemmed EO771, is it a well‐characterized cell line for mouse mammary cancer model? Limit and uncertainty
title_short EO771, is it a well‐characterized cell line for mouse mammary cancer model? Limit and uncertainty
title_sort eo771, is it a well‐characterized cell line for mouse mammary cancer model? limit and uncertainty
topic Cancer Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7643677/
https://www.ncbi.nlm.nih.gov/pubmed/33026171
http://dx.doi.org/10.1002/cam4.3295
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