Metformin limits the tumourigenicity of iPS cells without affecting their pluripotency

The antidiabetic drug metformin efficiently circumvents the dilemma that in reducing the tumourigenicity of stem cells, their essence, specifically their pluripotency, must also be sacrificed. Metformin prevents the occurrence or drastically reduces the size and weight of teratoma-like masses after...

Full description

Bibliographic Details
Main Authors: Vazquez-Martin, Alejandro, Cufi, Sílvia, Lopez-Bonet, Eugeni, Corominas-Faja, Bruna, Oliveras-Ferraros, Cristina, Martin-Castillo, Begoña, Menendez, Javier A.
Format: Online
Language:English
Published: Nature Publishing Group 2012
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3520055/
id pubmed-3520055
recordtype oai_dc
spelling pubmed-35200552012-12-12 Metformin limits the tumourigenicity of iPS cells without affecting their pluripotency Vazquez-Martin, Alejandro Cufi, Sílvia Lopez-Bonet, Eugeni Corominas-Faja, Bruna Oliveras-Ferraros, Cristina Martin-Castillo, Begoña Menendez, Javier A. Article The antidiabetic drug metformin efficiently circumvents the dilemma that in reducing the tumourigenicity of stem cells, their essence, specifically their pluripotency, must also be sacrificed. Metformin prevents the occurrence or drastically reduces the size and weight of teratoma-like masses after the transplantation of induced pluripotent stem (iPS) cells into immunodeficient mice. Yet, iPS cells implanted into metformin-treated mice retain full pluripotency, as they produce the same number of distinct tissue types derived from the three embryonic germ layers that is observed in untreated mice. Mechanistically, metformin appears to suppress the Oct4-driven compartment of malignant stem cells responsible for teratocarcinoma growth while safeguarding an intact, Oct4-independent competency to generate terminally differentiated tissues. Metformin's ability to efficiently and specifically control the tumourigenic fate of teratoma-initiating iPS cells without interfering with their pluripotency not only has implications for the clinical use of iPS cells but also in stem cell biology, cancer and ageing. Nature Publishing Group 2012-12-12 /pmc/articles/PMC3520055/ /pubmed/23236586 http://dx.doi.org/10.1038/srep00964 Text en Copyright © 2012, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Vazquez-Martin, Alejandro
Cufi, Sílvia
Lopez-Bonet, Eugeni
Corominas-Faja, Bruna
Oliveras-Ferraros, Cristina
Martin-Castillo, Begoña
Menendez, Javier A.
spellingShingle Vazquez-Martin, Alejandro
Cufi, Sílvia
Lopez-Bonet, Eugeni
Corominas-Faja, Bruna
Oliveras-Ferraros, Cristina
Martin-Castillo, Begoña
Menendez, Javier A.
Metformin limits the tumourigenicity of iPS cells without affecting their pluripotency
author_facet Vazquez-Martin, Alejandro
Cufi, Sílvia
Lopez-Bonet, Eugeni
Corominas-Faja, Bruna
Oliveras-Ferraros, Cristina
Martin-Castillo, Begoña
Menendez, Javier A.
author_sort Vazquez-Martin, Alejandro
title Metformin limits the tumourigenicity of iPS cells without affecting their pluripotency
title_short Metformin limits the tumourigenicity of iPS cells without affecting their pluripotency
title_full Metformin limits the tumourigenicity of iPS cells without affecting their pluripotency
title_fullStr Metformin limits the tumourigenicity of iPS cells without affecting their pluripotency
title_full_unstemmed Metformin limits the tumourigenicity of iPS cells without affecting their pluripotency
title_sort metformin limits the tumourigenicity of ips cells without affecting their pluripotency
description The antidiabetic drug metformin efficiently circumvents the dilemma that in reducing the tumourigenicity of stem cells, their essence, specifically their pluripotency, must also be sacrificed. Metformin prevents the occurrence or drastically reduces the size and weight of teratoma-like masses after the transplantation of induced pluripotent stem (iPS) cells into immunodeficient mice. Yet, iPS cells implanted into metformin-treated mice retain full pluripotency, as they produce the same number of distinct tissue types derived from the three embryonic germ layers that is observed in untreated mice. Mechanistically, metformin appears to suppress the Oct4-driven compartment of malignant stem cells responsible for teratocarcinoma growth while safeguarding an intact, Oct4-independent competency to generate terminally differentiated tissues. Metformin's ability to efficiently and specifically control the tumourigenic fate of teratoma-initiating iPS cells without interfering with their pluripotency not only has implications for the clinical use of iPS cells but also in stem cell biology, cancer and ageing.
publisher Nature Publishing Group
publishDate 2012
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3520055/
_version_ 1611939780267868160