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Induced pluripotent stem cells and personalized medicine: current progress and future perspectives

Generation of induced pluripotent stem cells (iPSCs) has revolutionized the field of regenerative medicine by providing researchers with a unique tool to derive disease-specific stem cells for study. iPSCs can self-renew and can differentiate into many cell types, offering a potentially unlimited so...

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Detalles Bibliográficos
Autores principales: Chun, Yong Soon, Byun, Kyunghee, Lee, Bonghee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Association of Anatomists 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3254878/
https://www.ncbi.nlm.nih.gov/pubmed/22254153
http://dx.doi.org/10.5115/acb.2011.44.4.245
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author Chun, Yong Soon
Byun, Kyunghee
Lee, Bonghee
author_facet Chun, Yong Soon
Byun, Kyunghee
Lee, Bonghee
author_sort Chun, Yong Soon
collection PubMed
description Generation of induced pluripotent stem cells (iPSCs) has revolutionized the field of regenerative medicine by providing researchers with a unique tool to derive disease-specific stem cells for study. iPSCs can self-renew and can differentiate into many cell types, offering a potentially unlimited source of cells for targeted differentiation into somatic effector cells. Hence, iPSCs are likely to be invaluable for therapeutic applications and disease-related research. In this review, we summarize the recent progress of iPSC generation that has been made with an emphasis on both basic and clinical applications including disease modeling, drug toxicity screening/drug discovery and cell replacement therapy.
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spelling pubmed-32548782012-01-17 Induced pluripotent stem cells and personalized medicine: current progress and future perspectives Chun, Yong Soon Byun, Kyunghee Lee, Bonghee Anat Cell Biol Review Article Generation of induced pluripotent stem cells (iPSCs) has revolutionized the field of regenerative medicine by providing researchers with a unique tool to derive disease-specific stem cells for study. iPSCs can self-renew and can differentiate into many cell types, offering a potentially unlimited source of cells for targeted differentiation into somatic effector cells. Hence, iPSCs are likely to be invaluable for therapeutic applications and disease-related research. In this review, we summarize the recent progress of iPSC generation that has been made with an emphasis on both basic and clinical applications including disease modeling, drug toxicity screening/drug discovery and cell replacement therapy. Korean Association of Anatomists 2011-12 2011-12-30 /pmc/articles/PMC3254878/ /pubmed/22254153 http://dx.doi.org/10.5115/acb.2011.44.4.245 Text en Copyright © 2011. Anatomy & Cell Biology http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Chun, Yong Soon
Byun, Kyunghee
Lee, Bonghee
Induced pluripotent stem cells and personalized medicine: current progress and future perspectives
title Induced pluripotent stem cells and personalized medicine: current progress and future perspectives
title_full Induced pluripotent stem cells and personalized medicine: current progress and future perspectives
title_fullStr Induced pluripotent stem cells and personalized medicine: current progress and future perspectives
title_full_unstemmed Induced pluripotent stem cells and personalized medicine: current progress and future perspectives
title_short Induced pluripotent stem cells and personalized medicine: current progress and future perspectives
title_sort induced pluripotent stem cells and personalized medicine: current progress and future perspectives
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3254878/
https://www.ncbi.nlm.nih.gov/pubmed/22254153
http://dx.doi.org/10.5115/acb.2011.44.4.245
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