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Activation of mammalian target of rapamycin (mTOR) in triple negative feline mammary carcinomas
BACKGROUND: Triple negative breast cancer (TNBC) in humans is defined by the absence of oestrogen receptor (ER), progesterone receptor (PR) and HER2 overexpression. Mammalian target of rapamycin (mTOR) is overexpressed in TNBC and it represents a potential target for the treatment of this aggressive...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3637810/ https://www.ncbi.nlm.nih.gov/pubmed/23587222 http://dx.doi.org/10.1186/1746-6148-9-80 |
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author | Maniscalco, Lorella Millán, Yolanda Iussich, Selina Denina, Mauro Sánchez-Céspedes, Raquel Gattino, Francesca Biolatti, Bartolomeo Sasaki, Nobuo Nakagawa, Takayuki Di Renzo, Maria Flavia de las Mulas, Juana Martín De Maria, Raffaella |
author_facet | Maniscalco, Lorella Millán, Yolanda Iussich, Selina Denina, Mauro Sánchez-Céspedes, Raquel Gattino, Francesca Biolatti, Bartolomeo Sasaki, Nobuo Nakagawa, Takayuki Di Renzo, Maria Flavia de las Mulas, Juana Martín De Maria, Raffaella |
author_sort | Maniscalco, Lorella |
collection | PubMed |
description | BACKGROUND: Triple negative breast cancer (TNBC) in humans is defined by the absence of oestrogen receptor (ER), progesterone receptor (PR) and HER2 overexpression. Mammalian target of rapamycin (mTOR) is overexpressed in TNBC and it represents a potential target for the treatment of this aggressive tumour. Feline mammary carcinoma (FMC) is considered to be a model for hormone-independent human breast cancer. This study investigated mTOR and p-mTOR expression in FMC in relation to triple negative (TN) phenotype. RESULTS: The expression of mTOR, p-mTOR, ERα, PR and HER2 was evaluated in 58 FMCs by immunohistochemistry and in six FMC cell lines by Western blot analysis. 53.5% of FMC analyzed were ER, PR, HER2 negative (TN-FMC) while 56.9% and 55.2% of cases expressed mTOR and p-mTOR respectively. In this study we found that m-TOR and p-mTOR were more frequently detected in TN-FMC and in HER2 negative samples. CONCLUSIONS: In this study, we demonstrate that there is also a FMC subset defined as TN FMC, which is characterised by a statistically significant association with m-TOR and p-mTOR expression as demonstrated in human breast cancer. |
format | Online Article Text |
id | pubmed-3637810 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-36378102013-04-28 Activation of mammalian target of rapamycin (mTOR) in triple negative feline mammary carcinomas Maniscalco, Lorella Millán, Yolanda Iussich, Selina Denina, Mauro Sánchez-Céspedes, Raquel Gattino, Francesca Biolatti, Bartolomeo Sasaki, Nobuo Nakagawa, Takayuki Di Renzo, Maria Flavia de las Mulas, Juana Martín De Maria, Raffaella BMC Vet Res Research Article BACKGROUND: Triple negative breast cancer (TNBC) in humans is defined by the absence of oestrogen receptor (ER), progesterone receptor (PR) and HER2 overexpression. Mammalian target of rapamycin (mTOR) is overexpressed in TNBC and it represents a potential target for the treatment of this aggressive tumour. Feline mammary carcinoma (FMC) is considered to be a model for hormone-independent human breast cancer. This study investigated mTOR and p-mTOR expression in FMC in relation to triple negative (TN) phenotype. RESULTS: The expression of mTOR, p-mTOR, ERα, PR and HER2 was evaluated in 58 FMCs by immunohistochemistry and in six FMC cell lines by Western blot analysis. 53.5% of FMC analyzed were ER, PR, HER2 negative (TN-FMC) while 56.9% and 55.2% of cases expressed mTOR and p-mTOR respectively. In this study we found that m-TOR and p-mTOR were more frequently detected in TN-FMC and in HER2 negative samples. CONCLUSIONS: In this study, we demonstrate that there is also a FMC subset defined as TN FMC, which is characterised by a statistically significant association with m-TOR and p-mTOR expression as demonstrated in human breast cancer. BioMed Central 2013-04-15 /pmc/articles/PMC3637810/ /pubmed/23587222 http://dx.doi.org/10.1186/1746-6148-9-80 Text en Copyright © 2013 Maniscalco et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Maniscalco, Lorella Millán, Yolanda Iussich, Selina Denina, Mauro Sánchez-Céspedes, Raquel Gattino, Francesca Biolatti, Bartolomeo Sasaki, Nobuo Nakagawa, Takayuki Di Renzo, Maria Flavia de las Mulas, Juana Martín De Maria, Raffaella Activation of mammalian target of rapamycin (mTOR) in triple negative feline mammary carcinomas |
title | Activation of mammalian target of rapamycin (mTOR) in triple negative feline mammary carcinomas |
title_full | Activation of mammalian target of rapamycin (mTOR) in triple negative feline mammary carcinomas |
title_fullStr | Activation of mammalian target of rapamycin (mTOR) in triple negative feline mammary carcinomas |
title_full_unstemmed | Activation of mammalian target of rapamycin (mTOR) in triple negative feline mammary carcinomas |
title_short | Activation of mammalian target of rapamycin (mTOR) in triple negative feline mammary carcinomas |
title_sort | activation of mammalian target of rapamycin (mtor) in triple negative feline mammary carcinomas |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3637810/ https://www.ncbi.nlm.nih.gov/pubmed/23587222 http://dx.doi.org/10.1186/1746-6148-9-80 |
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