Cargando…

Acidic Fibroblast Growth Factor in Spinal Cord Injury

Spinal cord injury (SCI), with an incidence rate of 246 per million person-years among adults in Taiwan, remains a devastating disease in the modern day. Elderly men with lower socioeconomic status have an even higher risk for SCI. Despite advances made in medicine and technology to date, there are...

Descripción completa

Detalles Bibliográficos
Autores principales: Ko, Chin-Chu, Tu, Tsung-Hsi, Wu, Jau-Ching, Huang, Wen-Cheng, Cheng, Henrich
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Spinal Neurosurgery Society 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6944993/
https://www.ncbi.nlm.nih.gov/pubmed/30653905
http://dx.doi.org/10.14245/ns.1836216.108
_version_ 1783485104178331648
author Ko, Chin-Chu
Tu, Tsung-Hsi
Wu, Jau-Ching
Huang, Wen-Cheng
Cheng, Henrich
author_facet Ko, Chin-Chu
Tu, Tsung-Hsi
Wu, Jau-Ching
Huang, Wen-Cheng
Cheng, Henrich
author_sort Ko, Chin-Chu
collection PubMed
description Spinal cord injury (SCI), with an incidence rate of 246 per million person-years among adults in Taiwan, remains a devastating disease in the modern day. Elderly men with lower socioeconomic status have an even higher risk for SCI. Despite advances made in medicine and technology to date, there are few effective treatments for SCI due to limitations in the regenerative capacity of the adult central nervous system. Experiments and clinical trials have explored neuro-regeneration in human SCI, encompassing cell- and molecule-based therapies. Furthermore, strategies have aimed at restoring connections, including autologous peripheral nerve grafts and biomaterial scaffolds that theoretically promote axonal growth. Most molecule-based therapies target the modulation of inhibitory molecules to promote axonal growth, degrade glial scarring obstacles, and stimulate intrinsic regenerative capacity. Among them, acidic fibroblast growth factor (aFGF) has been investigated for nerve repair; it is mitogenic and pluripotent in nature and could enhance axonal growth and mitigate glial scarring. For more than 2 decades, the authors have conducted multiple trials, including human and animal experiments, using aFGF to repair nerve injuries, including central and peripheral nerves. In these trials, aFGF has shown promise for neural regeneration, and in the future, more trials and applications should investigate aFGF as a neurotrophic factor. Focusing on aFGF, the current review aimed to summarize the historical evolution of the utilization of aFGF in SCI and nerve injuries, to present applications and trials, to summarize briefly its possible mechanisms, and to provide future perspectives.
format Online
Article
Text
id pubmed-6944993
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Korean Spinal Neurosurgery Society
record_format MEDLINE/PubMed
spelling pubmed-69449932020-01-14 Acidic Fibroblast Growth Factor in Spinal Cord Injury Ko, Chin-Chu Tu, Tsung-Hsi Wu, Jau-Ching Huang, Wen-Cheng Cheng, Henrich Neurospine Review Article Spinal cord injury (SCI), with an incidence rate of 246 per million person-years among adults in Taiwan, remains a devastating disease in the modern day. Elderly men with lower socioeconomic status have an even higher risk for SCI. Despite advances made in medicine and technology to date, there are few effective treatments for SCI due to limitations in the regenerative capacity of the adult central nervous system. Experiments and clinical trials have explored neuro-regeneration in human SCI, encompassing cell- and molecule-based therapies. Furthermore, strategies have aimed at restoring connections, including autologous peripheral nerve grafts and biomaterial scaffolds that theoretically promote axonal growth. Most molecule-based therapies target the modulation of inhibitory molecules to promote axonal growth, degrade glial scarring obstacles, and stimulate intrinsic regenerative capacity. Among them, acidic fibroblast growth factor (aFGF) has been investigated for nerve repair; it is mitogenic and pluripotent in nature and could enhance axonal growth and mitigate glial scarring. For more than 2 decades, the authors have conducted multiple trials, including human and animal experiments, using aFGF to repair nerve injuries, including central and peripheral nerves. In these trials, aFGF has shown promise for neural regeneration, and in the future, more trials and applications should investigate aFGF as a neurotrophic factor. Focusing on aFGF, the current review aimed to summarize the historical evolution of the utilization of aFGF in SCI and nerve injuries, to present applications and trials, to summarize briefly its possible mechanisms, and to provide future perspectives. Korean Spinal Neurosurgery Society 2019-12 2019-01-15 /pmc/articles/PMC6944993/ /pubmed/30653905 http://dx.doi.org/10.14245/ns.1836216.108 Text en Copyright © 2019 by the Korean Spinal Neurosurgery Society This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Ko, Chin-Chu
Tu, Tsung-Hsi
Wu, Jau-Ching
Huang, Wen-Cheng
Cheng, Henrich
Acidic Fibroblast Growth Factor in Spinal Cord Injury
title Acidic Fibroblast Growth Factor in Spinal Cord Injury
title_full Acidic Fibroblast Growth Factor in Spinal Cord Injury
title_fullStr Acidic Fibroblast Growth Factor in Spinal Cord Injury
title_full_unstemmed Acidic Fibroblast Growth Factor in Spinal Cord Injury
title_short Acidic Fibroblast Growth Factor in Spinal Cord Injury
title_sort acidic fibroblast growth factor in spinal cord injury
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6944993/
https://www.ncbi.nlm.nih.gov/pubmed/30653905
http://dx.doi.org/10.14245/ns.1836216.108
work_keys_str_mv AT kochinchu acidicfibroblastgrowthfactorinspinalcordinjury
AT tutsunghsi acidicfibroblastgrowthfactorinspinalcordinjury
AT wujauching acidicfibroblastgrowthfactorinspinalcordinjury
AT huangwencheng acidicfibroblastgrowthfactorinspinalcordinjury
AT chenghenrich acidicfibroblastgrowthfactorinspinalcordinjury