Neurotrophic growth factors for the treatment of amyotrophic lateral sclerosis: where do we stand ?

Amyotrophic lateral sclerosis (ALS) is a devastating neurodegenerative disease that results in progressive loss of motoneurons, motor weakness and death within 3-5 years after disease onset. Therapeutic options remain limited despite substantial number of approaches that have been tested clinically....

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Main Authors: Alexandre Henriques, Claudia Pitzer, Armin Schneider
Format: Article
Language:English
Published: Frontiers Media S.A. 2010-06-01
Series:Frontiers in Neuroscience
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fnins.2010.00032/full
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spelling doaj-6bc8c3a9614b49c4b16f45d55e4128662020-11-24T21:02:29ZengFrontiers Media S.A.Frontiers in Neuroscience1662-453X2010-06-01410.3389/fnins.2010.000321463Neurotrophic growth factors for the treatment of amyotrophic lateral sclerosis: where do we stand ?Alexandre Henriques0Alexandre Henriques1Alexandre Henriques2Claudia Pitzer3Armin Schneider4Institut National de la Santé et de la Recherche Médicale U692SYGNIS BioscienceUniversity of StrasbourgSYGNIS BioscienceSYGNIS BioscienceAmyotrophic lateral sclerosis (ALS) is a devastating neurodegenerative disease that results in progressive loss of motoneurons, motor weakness and death within 3-5 years after disease onset. Therapeutic options remain limited despite substantial number of approaches that have been tested clinically. Many neurotrophic growth factors are known to promote the survival of neurons and foster regeneration in the CNS. Various neurotrophic factors have been investigated preclinically and clinically for the treatment of ALS. Although preclinical data appeared promising, no neurotrophic factors succeeded yet in a clinical phase III trial. In this review we discuss the rationale behind those factors, possible reasons for clinical failures, and argue for a renewal of hope in this powerful class of drugs for the treatment of ALS.http://journal.frontiersin.org/Journal/10.3389/fnins.2010.00032/fullAmyotrophic Lateral Sclerosistherapyanimal modelClinical Trialgrowth factorsmotoneurons
collection DOAJ
language English
format Article
sources DOAJ
author Alexandre Henriques
Alexandre Henriques
Alexandre Henriques
Claudia Pitzer
Armin Schneider
spellingShingle Alexandre Henriques
Alexandre Henriques
Alexandre Henriques
Claudia Pitzer
Armin Schneider
Neurotrophic growth factors for the treatment of amyotrophic lateral sclerosis: where do we stand ?
Frontiers in Neuroscience
Amyotrophic Lateral Sclerosis
therapy
animal model
Clinical Trial
growth factors
motoneurons
author_facet Alexandre Henriques
Alexandre Henriques
Alexandre Henriques
Claudia Pitzer
Armin Schneider
author_sort Alexandre Henriques
title Neurotrophic growth factors for the treatment of amyotrophic lateral sclerosis: where do we stand ?
title_short Neurotrophic growth factors for the treatment of amyotrophic lateral sclerosis: where do we stand ?
title_full Neurotrophic growth factors for the treatment of amyotrophic lateral sclerosis: where do we stand ?
title_fullStr Neurotrophic growth factors for the treatment of amyotrophic lateral sclerosis: where do we stand ?
title_full_unstemmed Neurotrophic growth factors for the treatment of amyotrophic lateral sclerosis: where do we stand ?
title_sort neurotrophic growth factors for the treatment of amyotrophic lateral sclerosis: where do we stand ?
publisher Frontiers Media S.A.
series Frontiers in Neuroscience
issn 1662-453X
publishDate 2010-06-01
description Amyotrophic lateral sclerosis (ALS) is a devastating neurodegenerative disease that results in progressive loss of motoneurons, motor weakness and death within 3-5 years after disease onset. Therapeutic options remain limited despite substantial number of approaches that have been tested clinically. Many neurotrophic growth factors are known to promote the survival of neurons and foster regeneration in the CNS. Various neurotrophic factors have been investigated preclinically and clinically for the treatment of ALS. Although preclinical data appeared promising, no neurotrophic factors succeeded yet in a clinical phase III trial. In this review we discuss the rationale behind those factors, possible reasons for clinical failures, and argue for a renewal of hope in this powerful class of drugs for the treatment of ALS.
topic Amyotrophic Lateral Sclerosis
therapy
animal model
Clinical Trial
growth factors
motoneurons
url http://journal.frontiersin.org/Journal/10.3389/fnins.2010.00032/full
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