Cargando…

Molecular Biology and Clinical Mitigation of Cancer Treatment-Induced Neuropathy

Disruption of microtubule function is the antitumor mechanism of several classes of drugs used to treat cancer today. However, the significant beneficial effect on tumor outcomes is frequently counterbalanced by neurotoxic complications. Despite an abundance of scientific data, our under-standing of...

Descripción completa

Detalles Bibliográficos
Autores principales: Higa, Gerald M., Sypult, Corbin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Libertas Academica 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4820064/
https://www.ncbi.nlm.nih.gov/pubmed/27081324
http://dx.doi.org/10.4137/CMO.S32810
_version_ 1782425329787207680
author Higa, Gerald M.
Sypult, Corbin
author_facet Higa, Gerald M.
Sypult, Corbin
author_sort Higa, Gerald M.
collection PubMed
description Disruption of microtubule function is the antitumor mechanism of several classes of drugs used to treat cancer today. However, the significant beneficial effect on tumor outcomes is frequently counterbalanced by neurotoxic complications. Despite an abundance of scientific data, our under-standing of the biological mechanisms underlying this toxic reaction remains unclear, further hindering attempts to identify and develop effective preventive strategies. The primary goals of this review are to: (1) provide insight regarding the biology of the microtubule, (2) analyze the molecular and biochemical pathways that may be involved in the development of neurotoxicity, and (3) propose a unifying concept linking drug-induced neuropathy, microtubule dysfunction, and vitamin D.
format Online
Article
Text
id pubmed-4820064
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Libertas Academica
record_format MEDLINE/PubMed
spelling pubmed-48200642016-04-14 Molecular Biology and Clinical Mitigation of Cancer Treatment-Induced Neuropathy Higa, Gerald M. Sypult, Corbin Clin Med Insights Oncol Review Disruption of microtubule function is the antitumor mechanism of several classes of drugs used to treat cancer today. However, the significant beneficial effect on tumor outcomes is frequently counterbalanced by neurotoxic complications. Despite an abundance of scientific data, our under-standing of the biological mechanisms underlying this toxic reaction remains unclear, further hindering attempts to identify and develop effective preventive strategies. The primary goals of this review are to: (1) provide insight regarding the biology of the microtubule, (2) analyze the molecular and biochemical pathways that may be involved in the development of neurotoxicity, and (3) propose a unifying concept linking drug-induced neuropathy, microtubule dysfunction, and vitamin D. Libertas Academica 2016-04-03 /pmc/articles/PMC4820064/ /pubmed/27081324 http://dx.doi.org/10.4137/CMO.S32810 Text en © 2016 the author(s), publisher and licensee Libertas Academica Ltd. This is an open access article published under the Creative Commons CC-BY-NC 3.0 license.
spellingShingle Review
Higa, Gerald M.
Sypult, Corbin
Molecular Biology and Clinical Mitigation of Cancer Treatment-Induced Neuropathy
title Molecular Biology and Clinical Mitigation of Cancer Treatment-Induced Neuropathy
title_full Molecular Biology and Clinical Mitigation of Cancer Treatment-Induced Neuropathy
title_fullStr Molecular Biology and Clinical Mitigation of Cancer Treatment-Induced Neuropathy
title_full_unstemmed Molecular Biology and Clinical Mitigation of Cancer Treatment-Induced Neuropathy
title_short Molecular Biology and Clinical Mitigation of Cancer Treatment-Induced Neuropathy
title_sort molecular biology and clinical mitigation of cancer treatment-induced neuropathy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4820064/
https://www.ncbi.nlm.nih.gov/pubmed/27081324
http://dx.doi.org/10.4137/CMO.S32810
work_keys_str_mv AT higageraldm molecularbiologyandclinicalmitigationofcancertreatmentinducedneuropathy
AT sypultcorbin molecularbiologyandclinicalmitigationofcancertreatmentinducedneuropathy