Amyotrophic lateral sclerosis: applications of stem cells – an update

Lidia Cova1, Vincenzo Silani21Department of Neurology and Laboratory of Neuroscience, IRCCS Istituto Auxologico Italiano, Milano, Italy; 2Department of Neurology and Laboratory of Neuroscience, “Dino Ferrari” Center, Università degli Studi di Milano, IRCCS...

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Main Authors: Lidia Cova, Vincenzo Silani
Format: Article
Language:English
Published: Dove Medical Press 2010-10-01
Series:Stem Cells and Cloning : Advances and Applications
Online Access:http://www.dovepress.com/amyotrophic-lateral-sclerosis-applications-of-stem-cells-ndash-an-upda-a5557
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spelling doaj-29713822dba6480e84cf7b14d6b7400d2020-11-25T00:35:34ZengDove Medical PressStem Cells and Cloning : Advances and Applications1178-69572010-10-012010default145156Amyotrophic lateral sclerosis: applications of stem cells – an updateLidia CovaVincenzo SilaniLidia Cova1, Vincenzo Silani21Department of Neurology and Laboratory of Neuroscience, IRCCS Istituto Auxologico Italiano, Milano, Italy; 2Department of Neurology and Laboratory of Neuroscience, “Dino Ferrari” Center, Università degli Studi di Milano, IRCCS Istituto Auxologico Italiano, Milano, ItalyAbstract: Neurodegenerative diseases are a growing public health challenge, and amyotrophic lateral sclerosis (ALS) remains a fatal incurable disease. The advent of stem cell therapy has opened new horizons for both researchers and ALS patients, desperately looking for a treatment. ALS must be considered a systemic disease affecting many cell phenotypes besides motor neurons, even outside the central nervous system. Cell replacement therapy needs to address the specific neurobiological issues of ALS to safely and efficiently reach clinical settings. Moreover, the enormous potential of induced pluripotent cells directly derived from patients for modeling and understanding the pathological mechanisms, in correlation with the discoveries of new genes and animal models, provides new opportunities that need to be integrated with previously described transplantation strategies. Finally, a careful evaluation of preclinical data in conjunction with wary patient choice in clinical trials needs to be established in order to generate meaningful results.Keywords: amyotrophic lateral sclerosis, regenerative medicine, stem cell therapy, clinical trials http://www.dovepress.com/amyotrophic-lateral-sclerosis-applications-of-stem-cells-ndash-an-upda-a5557
collection DOAJ
language English
format Article
sources DOAJ
author Lidia Cova
Vincenzo Silani
spellingShingle Lidia Cova
Vincenzo Silani
Amyotrophic lateral sclerosis: applications of stem cells – an update
Stem Cells and Cloning : Advances and Applications
author_facet Lidia Cova
Vincenzo Silani
author_sort Lidia Cova
title Amyotrophic lateral sclerosis: applications of stem cells – an update
title_short Amyotrophic lateral sclerosis: applications of stem cells – an update
title_full Amyotrophic lateral sclerosis: applications of stem cells – an update
title_fullStr Amyotrophic lateral sclerosis: applications of stem cells – an update
title_full_unstemmed Amyotrophic lateral sclerosis: applications of stem cells – an update
title_sort amyotrophic lateral sclerosis: applications of stem cells – an update
publisher Dove Medical Press
series Stem Cells and Cloning : Advances and Applications
issn 1178-6957
publishDate 2010-10-01
description Lidia Cova1, Vincenzo Silani21Department of Neurology and Laboratory of Neuroscience, IRCCS Istituto Auxologico Italiano, Milano, Italy; 2Department of Neurology and Laboratory of Neuroscience, “Dino Ferrari” Center, Università degli Studi di Milano, IRCCS Istituto Auxologico Italiano, Milano, ItalyAbstract: Neurodegenerative diseases are a growing public health challenge, and amyotrophic lateral sclerosis (ALS) remains a fatal incurable disease. The advent of stem cell therapy has opened new horizons for both researchers and ALS patients, desperately looking for a treatment. ALS must be considered a systemic disease affecting many cell phenotypes besides motor neurons, even outside the central nervous system. Cell replacement therapy needs to address the specific neurobiological issues of ALS to safely and efficiently reach clinical settings. Moreover, the enormous potential of induced pluripotent cells directly derived from patients for modeling and understanding the pathological mechanisms, in correlation with the discoveries of new genes and animal models, provides new opportunities that need to be integrated with previously described transplantation strategies. Finally, a careful evaluation of preclinical data in conjunction with wary patient choice in clinical trials needs to be established in order to generate meaningful results.Keywords: amyotrophic lateral sclerosis, regenerative medicine, stem cell therapy, clinical trials
url http://www.dovepress.com/amyotrophic-lateral-sclerosis-applications-of-stem-cells-ndash-an-upda-a5557
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