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Clinical development of mTOR inhibitors in breast cancer

The mammalian target of rapamycin (mTOR) pathway is a central pathway that regulates mRNA translation, protein synthesis, glucose metabolism, lipid synthesis and autophagy, and is involved in malignant transformation. Several randomized trials have shown that the use of mTOR inhibitors could improve...

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Autores principales: Vicier, Cecile, Dieci, Maria Vittoria, Arnedos, Monica, Delaloge, Suzette, Viens, Patrice, Andre, Fabrice
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3978635/
https://www.ncbi.nlm.nih.gov/pubmed/25189767
http://dx.doi.org/10.1186/bcr3618
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author Vicier, Cecile
Dieci, Maria Vittoria
Arnedos, Monica
Delaloge, Suzette
Viens, Patrice
Andre, Fabrice
author_facet Vicier, Cecile
Dieci, Maria Vittoria
Arnedos, Monica
Delaloge, Suzette
Viens, Patrice
Andre, Fabrice
author_sort Vicier, Cecile
collection PubMed
description The mammalian target of rapamycin (mTOR) pathway is a central pathway that regulates mRNA translation, protein synthesis, glucose metabolism, lipid synthesis and autophagy, and is involved in malignant transformation. Several randomized trials have shown that the use of mTOR inhibitors could improve patient outcome with hormone receptor-positive or human epidermal growth factor receptor-2-positive breast cancer. This review analyzes new perspectives from these trials. Preclinical studies have suggested that the mTOR pathway may play a role in the resistance to hormone therapy, trastuzumab and chemotherapy for breast cancer. This concept has been tested in clinical trials for neoadjuvant treatment and for metastatic breast cancer patients. Also, much effort has gone into the identification of biomarkers that will allow for more precise stratification of patients. Findings from these studies will provide indispensable tools for the design of future clinical trials and identify new perspectives and challenges for researchers and clinicians.
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spelling pubmed-39786352014-04-08 Clinical development of mTOR inhibitors in breast cancer Vicier, Cecile Dieci, Maria Vittoria Arnedos, Monica Delaloge, Suzette Viens, Patrice Andre, Fabrice Breast Cancer Res Review The mammalian target of rapamycin (mTOR) pathway is a central pathway that regulates mRNA translation, protein synthesis, glucose metabolism, lipid synthesis and autophagy, and is involved in malignant transformation. Several randomized trials have shown that the use of mTOR inhibitors could improve patient outcome with hormone receptor-positive or human epidermal growth factor receptor-2-positive breast cancer. This review analyzes new perspectives from these trials. Preclinical studies have suggested that the mTOR pathway may play a role in the resistance to hormone therapy, trastuzumab and chemotherapy for breast cancer. This concept has been tested in clinical trials for neoadjuvant treatment and for metastatic breast cancer patients. Also, much effort has gone into the identification of biomarkers that will allow for more precise stratification of patients. Findings from these studies will provide indispensable tools for the design of future clinical trials and identify new perspectives and challenges for researchers and clinicians. BioMed Central 2014 2014-02-17 /pmc/articles/PMC3978635/ /pubmed/25189767 http://dx.doi.org/10.1186/bcr3618 Text en Copyright © 2014 BioMed Central Ltd.
spellingShingle Review
Vicier, Cecile
Dieci, Maria Vittoria
Arnedos, Monica
Delaloge, Suzette
Viens, Patrice
Andre, Fabrice
Clinical development of mTOR inhibitors in breast cancer
title Clinical development of mTOR inhibitors in breast cancer
title_full Clinical development of mTOR inhibitors in breast cancer
title_fullStr Clinical development of mTOR inhibitors in breast cancer
title_full_unstemmed Clinical development of mTOR inhibitors in breast cancer
title_short Clinical development of mTOR inhibitors in breast cancer
title_sort clinical development of mtor inhibitors in breast cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3978635/
https://www.ncbi.nlm.nih.gov/pubmed/25189767
http://dx.doi.org/10.1186/bcr3618
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