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Improving therapeutic potential of GDNF family ligands

The last decade has been a frustrating time for investigators who had envisioned major advances in the treatment of Parkinson’s disease using neurotrophic factors. The first trials of glial cell line–derived neurotrophic factor for treating Parkinson’s disease were very promising. Later blinded cont...

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Detalles Bibliográficos
Autores principales: Runeberg-Roos, Pia, Penn, Richard D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7529618/
https://www.ncbi.nlm.nih.gov/pubmed/32725425
http://dx.doi.org/10.1007/s00441-020-03256-z
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author Runeberg-Roos, Pia
Penn, Richard D
author_facet Runeberg-Roos, Pia
Penn, Richard D
author_sort Runeberg-Roos, Pia
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description The last decade has been a frustrating time for investigators who had envisioned major advances in the treatment of Parkinson’s disease using neurotrophic factors. The first trials of glial cell line–derived neurotrophic factor for treating Parkinson’s disease were very promising. Later blinded control trials were disappointing, not reaching the predetermined outcomes for improvement in motor function. Consideration of the problems in the studies as well as the biology of the neurotrophins used can potentially lead to more effective therapies. Parkinson’s disease presents a multitude of opportunities for the cell biologist wanting to understand its pathology and to find possible new avenues for treatment.
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spelling pubmed-75296182020-10-19 Improving therapeutic potential of GDNF family ligands Runeberg-Roos, Pia Penn, Richard D Cell Tissue Res Review The last decade has been a frustrating time for investigators who had envisioned major advances in the treatment of Parkinson’s disease using neurotrophic factors. The first trials of glial cell line–derived neurotrophic factor for treating Parkinson’s disease were very promising. Later blinded control trials were disappointing, not reaching the predetermined outcomes for improvement in motor function. Consideration of the problems in the studies as well as the biology of the neurotrophins used can potentially lead to more effective therapies. Parkinson’s disease presents a multitude of opportunities for the cell biologist wanting to understand its pathology and to find possible new avenues for treatment. Springer Berlin Heidelberg 2020-07-28 2020 /pmc/articles/PMC7529618/ /pubmed/32725425 http://dx.doi.org/10.1007/s00441-020-03256-z Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Review
Runeberg-Roos, Pia
Penn, Richard D
Improving therapeutic potential of GDNF family ligands
title Improving therapeutic potential of GDNF family ligands
title_full Improving therapeutic potential of GDNF family ligands
title_fullStr Improving therapeutic potential of GDNF family ligands
title_full_unstemmed Improving therapeutic potential of GDNF family ligands
title_short Improving therapeutic potential of GDNF family ligands
title_sort improving therapeutic potential of gdnf family ligands
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7529618/
https://www.ncbi.nlm.nih.gov/pubmed/32725425
http://dx.doi.org/10.1007/s00441-020-03256-z
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