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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
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.
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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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