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The cell-autonomous mechanisms underlying the activity of metformin as an anticancer drug

The biguanide drug metformin profoundly affects cell metabolism, causing an impairment of the cell energy balance and triggering a plethora of pleiotropic effects that vary depending on the cellular or environmental context. Interestingly, a decade ago, it was observed that metformin-treated diabeti...

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Autores principales: Sacco, Francesca, Calderone, Alberto, Castagnoli, Luisa, Cesareni, Gianni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5155371/
https://www.ncbi.nlm.nih.gov/pubmed/27875520
http://dx.doi.org/10.1038/bjc.2016.385
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author Sacco, Francesca
Calderone, Alberto
Castagnoli, Luisa
Cesareni, Gianni
author_facet Sacco, Francesca
Calderone, Alberto
Castagnoli, Luisa
Cesareni, Gianni
author_sort Sacco, Francesca
collection PubMed
description The biguanide drug metformin profoundly affects cell metabolism, causing an impairment of the cell energy balance and triggering a plethora of pleiotropic effects that vary depending on the cellular or environmental context. Interestingly, a decade ago, it was observed that metformin-treated diabetic patients have a significantly lower cancer risk. Although a variety of in vivo and in vitro observations emphasising the role of metformin as anticancer drug have been reported, the underlying mechanisms are still poorly understood. Here, we discuss our current understanding of the molecular mechanisms that are perturbed by metformin treatment and that might be relevant to understand its antitumour activities. We focus on the cell-autonomous mechanisms modulating growth and death of cancer cells.
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spelling pubmed-51553712016-12-29 The cell-autonomous mechanisms underlying the activity of metformin as an anticancer drug Sacco, Francesca Calderone, Alberto Castagnoli, Luisa Cesareni, Gianni Br J Cancer Minireview The biguanide drug metformin profoundly affects cell metabolism, causing an impairment of the cell energy balance and triggering a plethora of pleiotropic effects that vary depending on the cellular or environmental context. Interestingly, a decade ago, it was observed that metformin-treated diabetic patients have a significantly lower cancer risk. Although a variety of in vivo and in vitro observations emphasising the role of metformin as anticancer drug have been reported, the underlying mechanisms are still poorly understood. Here, we discuss our current understanding of the molecular mechanisms that are perturbed by metformin treatment and that might be relevant to understand its antitumour activities. We focus on the cell-autonomous mechanisms modulating growth and death of cancer cells. Nature Publishing Group 2016-12-06 2016-11-22 /pmc/articles/PMC5155371/ /pubmed/27875520 http://dx.doi.org/10.1038/bjc.2016.385 Text en Copyright © 2016 The Author(s) http://creativecommons.org/licenses/by-nc-sa/4.0/ This work is licensed under the Creative Commons Attribution-Non-Commercial-Share Alike 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/
spellingShingle Minireview
Sacco, Francesca
Calderone, Alberto
Castagnoli, Luisa
Cesareni, Gianni
The cell-autonomous mechanisms underlying the activity of metformin as an anticancer drug
title The cell-autonomous mechanisms underlying the activity of metformin as an anticancer drug
title_full The cell-autonomous mechanisms underlying the activity of metformin as an anticancer drug
title_fullStr The cell-autonomous mechanisms underlying the activity of metformin as an anticancer drug
title_full_unstemmed The cell-autonomous mechanisms underlying the activity of metformin as an anticancer drug
title_short The cell-autonomous mechanisms underlying the activity of metformin as an anticancer drug
title_sort cell-autonomous mechanisms underlying the activity of metformin as an anticancer drug
topic Minireview
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5155371/
https://www.ncbi.nlm.nih.gov/pubmed/27875520
http://dx.doi.org/10.1038/bjc.2016.385
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