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Minoxidil is a potential neuroprotective drug for paclitaxel-induced peripheral neuropathy
Chemotherapy-induced peripheral neuropathy (CIPN) is a common side effect of cancer treatment. No medication has been shown to be effective in the treatment of CIPN. This study aims to integrate the image-based high-content screening, mouse behavior models and mechanistic cell-based assays to discov...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5368986/ https://www.ncbi.nlm.nih.gov/pubmed/28349969 http://dx.doi.org/10.1038/srep45366 |
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author | Chen, Yi-Fan Chen, Li-Hsien Yeh, Yu-Min Wu, Pei-Ying Chen, Yih-Fung Chang, Lian-Yun Chang, Jang-Yang Shen, Meng-Ru |
author_facet | Chen, Yi-Fan Chen, Li-Hsien Yeh, Yu-Min Wu, Pei-Ying Chen, Yih-Fung Chang, Lian-Yun Chang, Jang-Yang Shen, Meng-Ru |
author_sort | Chen, Yi-Fan |
collection | PubMed |
description | Chemotherapy-induced peripheral neuropathy (CIPN) is a common side effect of cancer treatment. No medication has been shown to be effective in the treatment of CIPN. This study aims to integrate the image-based high-content screening, mouse behavior models and mechanistic cell-based assays to discover potential neuroprotective drugs. Among screened compounds, minoxidil showed the most potent neuroprotective effect against paclitaxel, with regard to neurite outgrowth of dorsal root ganglia (DRG). Minoxidil protected mice from thermal insensitivity and alleviated mechanical allodynia in paclitaxel-treated mice. The ultrastructure and quantified G-ratio of myelin integrity of sciatic nerve tissues supported the observations in mouse behavioral tests. The mechanistic study on DRG neurons suggested that minoxidil suppressed neuroinflammation and remodeled the dysregulation of intracellular calcium homeostasis provoked by paclitaxel. Importantly, minoxidil showed a synergistic anti-tumor effect with paclitaxel both in tumor xenograft models of cervical and breast cancer. Interestingly, the quantitative assays on hair length and hair growth both exhibited that minoxidil significantly improved the hair quality after chemotherapy. Since minoxidil is a drug approved by the Food and Drug Administration (FDA), the safety and biocompatibility are well documented. The immediate next step is to launch an early-stage clinical trial intending to prevent CIPN by minoxidil. |
format | Online Article Text |
id | pubmed-5368986 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53689862017-03-30 Minoxidil is a potential neuroprotective drug for paclitaxel-induced peripheral neuropathy Chen, Yi-Fan Chen, Li-Hsien Yeh, Yu-Min Wu, Pei-Ying Chen, Yih-Fung Chang, Lian-Yun Chang, Jang-Yang Shen, Meng-Ru Sci Rep Article Chemotherapy-induced peripheral neuropathy (CIPN) is a common side effect of cancer treatment. No medication has been shown to be effective in the treatment of CIPN. This study aims to integrate the image-based high-content screening, mouse behavior models and mechanistic cell-based assays to discover potential neuroprotective drugs. Among screened compounds, minoxidil showed the most potent neuroprotective effect against paclitaxel, with regard to neurite outgrowth of dorsal root ganglia (DRG). Minoxidil protected mice from thermal insensitivity and alleviated mechanical allodynia in paclitaxel-treated mice. The ultrastructure and quantified G-ratio of myelin integrity of sciatic nerve tissues supported the observations in mouse behavioral tests. The mechanistic study on DRG neurons suggested that minoxidil suppressed neuroinflammation and remodeled the dysregulation of intracellular calcium homeostasis provoked by paclitaxel. Importantly, minoxidil showed a synergistic anti-tumor effect with paclitaxel both in tumor xenograft models of cervical and breast cancer. Interestingly, the quantitative assays on hair length and hair growth both exhibited that minoxidil significantly improved the hair quality after chemotherapy. Since minoxidil is a drug approved by the Food and Drug Administration (FDA), the safety and biocompatibility are well documented. The immediate next step is to launch an early-stage clinical trial intending to prevent CIPN by minoxidil. Nature Publishing Group 2017-03-28 /pmc/articles/PMC5368986/ /pubmed/28349969 http://dx.doi.org/10.1038/srep45366 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Chen, Yi-Fan Chen, Li-Hsien Yeh, Yu-Min Wu, Pei-Ying Chen, Yih-Fung Chang, Lian-Yun Chang, Jang-Yang Shen, Meng-Ru Minoxidil is a potential neuroprotective drug for paclitaxel-induced peripheral neuropathy |
title | Minoxidil is a potential neuroprotective drug for paclitaxel-induced peripheral neuropathy |
title_full | Minoxidil is a potential neuroprotective drug for paclitaxel-induced peripheral neuropathy |
title_fullStr | Minoxidil is a potential neuroprotective drug for paclitaxel-induced peripheral neuropathy |
title_full_unstemmed | Minoxidil is a potential neuroprotective drug for paclitaxel-induced peripheral neuropathy |
title_short | Minoxidil is a potential neuroprotective drug for paclitaxel-induced peripheral neuropathy |
title_sort | minoxidil is a potential neuroprotective drug for paclitaxel-induced peripheral neuropathy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5368986/ https://www.ncbi.nlm.nih.gov/pubmed/28349969 http://dx.doi.org/10.1038/srep45366 |
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