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Discovery of Potential Neuroprotective Agents against Paclitaxel-Induced Peripheral Neuropathy
[Image: see text] Chemotherapy-induced neurotoxicity is a common adverse effect of cancer treatment. No medication has been shown to be effective in the prevention or treatment of chemotherapy-induced neurotoxicity. Using minoxidil as an initial template for structural modifications in conjunction w...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8958505/ https://www.ncbi.nlm.nih.gov/pubmed/35234475 http://dx.doi.org/10.1021/acs.jmedchem.1c01912 |
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author | Chen, Yi-Fan Wu, Chien-Huang Chen, Li-Hsien Lee, Hao-Wei Lee, Jinq-Chyi Yeh, Teng-Kuang Chang, Jang-Yang Chou, Ming-Chen Wu, Hui-Ling Lai, Yen-Po Song, Jen-Shin Yeh, Kai-Chia Chen, Chiung-Tong Lee, Chia-Jui Shia, Kak-Shan Shen, Meng-Ru |
author_facet | Chen, Yi-Fan Wu, Chien-Huang Chen, Li-Hsien Lee, Hao-Wei Lee, Jinq-Chyi Yeh, Teng-Kuang Chang, Jang-Yang Chou, Ming-Chen Wu, Hui-Ling Lai, Yen-Po Song, Jen-Shin Yeh, Kai-Chia Chen, Chiung-Tong Lee, Chia-Jui Shia, Kak-Shan Shen, Meng-Ru |
author_sort | Chen, Yi-Fan |
collection | PubMed |
description | [Image: see text] Chemotherapy-induced neurotoxicity is a common adverse effect of cancer treatment. No medication has been shown to be effective in the prevention or treatment of chemotherapy-induced neurotoxicity. Using minoxidil as an initial template for structural modifications in conjunction with an in vitro neurite outgrowth assay, an image-based high-content screening platform, and mouse behavior models, an effective neuroprotective agent CN016 was discovered. Our results showed that CN016 could inhibit paclitaxel-induced inflammatory responses and infiltration of immune cells into sensory neurons significantly. Thus, the suppression of proinflammatory factors elucidates, in part, the mechanism of action of CN016 on alleviating paclitaxel-induced peripheral neuropathy. Based on excellent efficacy in improving behavioral functions, high safety profiles (MTD > 500 mg/kg), and a large therapeutic window (MTD/MED > 50) in mice, CN016 might have great potential to become a peripherally neuroprotective agent to prevent neurotoxicity caused by chemotherapeutics as typified by paclitaxel. |
format | Online Article Text |
id | pubmed-8958505 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-89585052022-03-29 Discovery of Potential Neuroprotective Agents against Paclitaxel-Induced Peripheral Neuropathy Chen, Yi-Fan Wu, Chien-Huang Chen, Li-Hsien Lee, Hao-Wei Lee, Jinq-Chyi Yeh, Teng-Kuang Chang, Jang-Yang Chou, Ming-Chen Wu, Hui-Ling Lai, Yen-Po Song, Jen-Shin Yeh, Kai-Chia Chen, Chiung-Tong Lee, Chia-Jui Shia, Kak-Shan Shen, Meng-Ru J Med Chem [Image: see text] Chemotherapy-induced neurotoxicity is a common adverse effect of cancer treatment. No medication has been shown to be effective in the prevention or treatment of chemotherapy-induced neurotoxicity. Using minoxidil as an initial template for structural modifications in conjunction with an in vitro neurite outgrowth assay, an image-based high-content screening platform, and mouse behavior models, an effective neuroprotective agent CN016 was discovered. Our results showed that CN016 could inhibit paclitaxel-induced inflammatory responses and infiltration of immune cells into sensory neurons significantly. Thus, the suppression of proinflammatory factors elucidates, in part, the mechanism of action of CN016 on alleviating paclitaxel-induced peripheral neuropathy. Based on excellent efficacy in improving behavioral functions, high safety profiles (MTD > 500 mg/kg), and a large therapeutic window (MTD/MED > 50) in mice, CN016 might have great potential to become a peripherally neuroprotective agent to prevent neurotoxicity caused by chemotherapeutics as typified by paclitaxel. American Chemical Society 2022-03-02 2022-03-24 /pmc/articles/PMC8958505/ /pubmed/35234475 http://dx.doi.org/10.1021/acs.jmedchem.1c01912 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Chen, Yi-Fan Wu, Chien-Huang Chen, Li-Hsien Lee, Hao-Wei Lee, Jinq-Chyi Yeh, Teng-Kuang Chang, Jang-Yang Chou, Ming-Chen Wu, Hui-Ling Lai, Yen-Po Song, Jen-Shin Yeh, Kai-Chia Chen, Chiung-Tong Lee, Chia-Jui Shia, Kak-Shan Shen, Meng-Ru Discovery of Potential Neuroprotective Agents against Paclitaxel-Induced Peripheral Neuropathy |
title | Discovery of Potential
Neuroprotective Agents against
Paclitaxel-Induced Peripheral Neuropathy |
title_full | Discovery of Potential
Neuroprotective Agents against
Paclitaxel-Induced Peripheral Neuropathy |
title_fullStr | Discovery of Potential
Neuroprotective Agents against
Paclitaxel-Induced Peripheral Neuropathy |
title_full_unstemmed | Discovery of Potential
Neuroprotective Agents against
Paclitaxel-Induced Peripheral Neuropathy |
title_short | Discovery of Potential
Neuroprotective Agents against
Paclitaxel-Induced Peripheral Neuropathy |
title_sort | discovery of potential
neuroprotective agents against
paclitaxel-induced peripheral neuropathy |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8958505/ https://www.ncbi.nlm.nih.gov/pubmed/35234475 http://dx.doi.org/10.1021/acs.jmedchem.1c01912 |
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