Systemic 5-fluorouracil treatment causes a syndrome of delayed myelin destruction in the central nervous system

<p>Abstract</p> <p>Background</p> <p>Cancer treatment with a variety of chemotherapeutic agents often is associated with delayed adverse neurological consequences. Despite their clinical importance, almost nothing is known about the basis for such effects. It is not eve...

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Main Authors: Han Ruolan, Yang Yin M, Dietrich Joerg, Luebke Anne, Mayer-Pröschel Margot, Noble Mark
Format: Article
Language:English
Published: BMC 2008-04-01
Series:Journal of Biology
Online Access:http://jbiol.com/content/7/4/12
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spelling doaj-083b865ac4174cba89ab59f0841333fc2020-11-25T00:16:48ZengBMCJournal of Biology1478-58541475-49242008-04-01741210.1186/jbiol69Systemic 5-fluorouracil treatment causes a syndrome of delayed myelin destruction in the central nervous systemHan RuolanYang Yin MDietrich JoergLuebke AnneMayer-Pröschel MargotNoble Mark<p>Abstract</p> <p>Background</p> <p>Cancer treatment with a variety of chemotherapeutic agents often is associated with delayed adverse neurological consequences. Despite their clinical importance, almost nothing is known about the basis for such effects. It is not even known whether the occurrence of delayed adverse effects requires exposure to multiple chemotherapeutic agents, the presence of both chemotherapeutic agents and the body's own response to cancer, prolonged damage to the blood-brain barrier, inflammation or other such changes. Nor are there any animal models that could enable the study of this important problem.</p> <p>Results</p> <p>We found that clinically relevant concentrations of 5-fluorouracil (5-FU; a widely used chemotherapeutic agent) were toxic for both central nervous system (CNS) progenitor cells and non-dividing oligodendrocytes <it>in vitro </it>and <it>in vivo</it>. Short-term systemic administration of 5-FU caused both acute CNS damage and a syndrome of progressively worsening delayed damage to myelinated tracts of the CNS associated with altered transcriptional regulation in oligodendrocytes and extensive myelin pathology. Functional analysis also provided the first demonstration of delayed effects of chemotherapy on the latency of impulse conduction in the auditory system, offering the possibility of non-invasive analysis of myelin damage associated with cancer treatment.</p> <p>Conclusions</p> <p>Our studies demonstrate that systemic treatment with a single chemotherapeutic agent, 5-FU, is sufficient to cause a syndrome of delayed CNS damage and provide the first animal model of delayed damage to white-matter tracts of individuals treated with systemic chemotherapy. Unlike that caused by local irradiation, the degeneration caused by 5-FU treatment did not correlate with either chronic inflammation or extensive vascular damage and appears to represent a new class of delayed degenerative damage in the CNS.</p> http://jbiol.com/content/7/4/12
collection DOAJ
language English
format Article
sources DOAJ
author Han Ruolan
Yang Yin M
Dietrich Joerg
Luebke Anne
Mayer-Pröschel Margot
Noble Mark
spellingShingle Han Ruolan
Yang Yin M
Dietrich Joerg
Luebke Anne
Mayer-Pröschel Margot
Noble Mark
Systemic 5-fluorouracil treatment causes a syndrome of delayed myelin destruction in the central nervous system
Journal of Biology
author_facet Han Ruolan
Yang Yin M
Dietrich Joerg
Luebke Anne
Mayer-Pröschel Margot
Noble Mark
author_sort Han Ruolan
title Systemic 5-fluorouracil treatment causes a syndrome of delayed myelin destruction in the central nervous system
title_short Systemic 5-fluorouracil treatment causes a syndrome of delayed myelin destruction in the central nervous system
title_full Systemic 5-fluorouracil treatment causes a syndrome of delayed myelin destruction in the central nervous system
title_fullStr Systemic 5-fluorouracil treatment causes a syndrome of delayed myelin destruction in the central nervous system
title_full_unstemmed Systemic 5-fluorouracil treatment causes a syndrome of delayed myelin destruction in the central nervous system
title_sort systemic 5-fluorouracil treatment causes a syndrome of delayed myelin destruction in the central nervous system
publisher BMC
series Journal of Biology
issn 1478-5854
1475-4924
publishDate 2008-04-01
description <p>Abstract</p> <p>Background</p> <p>Cancer treatment with a variety of chemotherapeutic agents often is associated with delayed adverse neurological consequences. Despite their clinical importance, almost nothing is known about the basis for such effects. It is not even known whether the occurrence of delayed adverse effects requires exposure to multiple chemotherapeutic agents, the presence of both chemotherapeutic agents and the body's own response to cancer, prolonged damage to the blood-brain barrier, inflammation or other such changes. Nor are there any animal models that could enable the study of this important problem.</p> <p>Results</p> <p>We found that clinically relevant concentrations of 5-fluorouracil (5-FU; a widely used chemotherapeutic agent) were toxic for both central nervous system (CNS) progenitor cells and non-dividing oligodendrocytes <it>in vitro </it>and <it>in vivo</it>. Short-term systemic administration of 5-FU caused both acute CNS damage and a syndrome of progressively worsening delayed damage to myelinated tracts of the CNS associated with altered transcriptional regulation in oligodendrocytes and extensive myelin pathology. Functional analysis also provided the first demonstration of delayed effects of chemotherapy on the latency of impulse conduction in the auditory system, offering the possibility of non-invasive analysis of myelin damage associated with cancer treatment.</p> <p>Conclusions</p> <p>Our studies demonstrate that systemic treatment with a single chemotherapeutic agent, 5-FU, is sufficient to cause a syndrome of delayed CNS damage and provide the first animal model of delayed damage to white-matter tracts of individuals treated with systemic chemotherapy. Unlike that caused by local irradiation, the degeneration caused by 5-FU treatment did not correlate with either chronic inflammation or extensive vascular damage and appears to represent a new class of delayed degenerative damage in the CNS.</p>
url http://jbiol.com/content/7/4/12
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