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DF2726A, a new IL-8 signalling inhibitor, is able to counteract chemotherapy-induced neuropathic pain
Chemotherapy-induced peripheral neuropathy (CIPN) is a common dose-limiting side effect of several anti-neoplastics and a main cause of sensory disturbances in cancer survivors, negatively impacting patients’ quality of life. Peripheral nerve degeneration or small fibre neuropathy is generally accep...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6692352/ https://www.ncbi.nlm.nih.gov/pubmed/31409858 http://dx.doi.org/10.1038/s41598-019-48231-z |
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author | Brandolini, Laura Castelli, Vanessa Aramini, Andrea Giorgio, Cristina Bianchini, Gianluca Russo, Roberto De Caro, Carmen d’Angelo, Michele Catanesi, Mariano Benedetti, Elisabetta Giordano, Antonio Cimini, Annamaria Allegretti, Marcello |
author_facet | Brandolini, Laura Castelli, Vanessa Aramini, Andrea Giorgio, Cristina Bianchini, Gianluca Russo, Roberto De Caro, Carmen d’Angelo, Michele Catanesi, Mariano Benedetti, Elisabetta Giordano, Antonio Cimini, Annamaria Allegretti, Marcello |
author_sort | Brandolini, Laura |
collection | PubMed |
description | Chemotherapy-induced peripheral neuropathy (CIPN) is a common dose-limiting side effect of several anti-neoplastics and a main cause of sensory disturbances in cancer survivors, negatively impacting patients’ quality of life. Peripheral nerve degeneration or small fibre neuropathy is generally accepted as the underlying mechanism in the development of CIPN. Recent evidence has contributed to clarify the determinant role of cytokines and chemokines in the process leading to neuronal hyperexcitability. Exposure to oxaliplatin triggers alterations in peripheral neuropathic pathways previously linked to IL-8 pathway. We investigated a novel selective inhibitor of IL-8 receptors, DF2726A, and showed its effects in counteracting CINP pathways, extending the relevance of the activation of IL-8 pathway to the class of platinum chemotherapeutics. Based on our results, we suggest that DF2726A might be a promising candidate for clinical treatment of CIPN conditions due to its efficacy and optimized pharmacokinetic/pharmacodynamic profile. |
format | Online Article Text |
id | pubmed-6692352 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-66923522019-08-19 DF2726A, a new IL-8 signalling inhibitor, is able to counteract chemotherapy-induced neuropathic pain Brandolini, Laura Castelli, Vanessa Aramini, Andrea Giorgio, Cristina Bianchini, Gianluca Russo, Roberto De Caro, Carmen d’Angelo, Michele Catanesi, Mariano Benedetti, Elisabetta Giordano, Antonio Cimini, Annamaria Allegretti, Marcello Sci Rep Article Chemotherapy-induced peripheral neuropathy (CIPN) is a common dose-limiting side effect of several anti-neoplastics and a main cause of sensory disturbances in cancer survivors, negatively impacting patients’ quality of life. Peripheral nerve degeneration or small fibre neuropathy is generally accepted as the underlying mechanism in the development of CIPN. Recent evidence has contributed to clarify the determinant role of cytokines and chemokines in the process leading to neuronal hyperexcitability. Exposure to oxaliplatin triggers alterations in peripheral neuropathic pathways previously linked to IL-8 pathway. We investigated a novel selective inhibitor of IL-8 receptors, DF2726A, and showed its effects in counteracting CINP pathways, extending the relevance of the activation of IL-8 pathway to the class of platinum chemotherapeutics. Based on our results, we suggest that DF2726A might be a promising candidate for clinical treatment of CIPN conditions due to its efficacy and optimized pharmacokinetic/pharmacodynamic profile. Nature Publishing Group UK 2019-08-13 /pmc/articles/PMC6692352/ /pubmed/31409858 http://dx.doi.org/10.1038/s41598-019-48231-z Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Brandolini, Laura Castelli, Vanessa Aramini, Andrea Giorgio, Cristina Bianchini, Gianluca Russo, Roberto De Caro, Carmen d’Angelo, Michele Catanesi, Mariano Benedetti, Elisabetta Giordano, Antonio Cimini, Annamaria Allegretti, Marcello DF2726A, a new IL-8 signalling inhibitor, is able to counteract chemotherapy-induced neuropathic pain |
title | DF2726A, a new IL-8 signalling inhibitor, is able to counteract chemotherapy-induced neuropathic pain |
title_full | DF2726A, a new IL-8 signalling inhibitor, is able to counteract chemotherapy-induced neuropathic pain |
title_fullStr | DF2726A, a new IL-8 signalling inhibitor, is able to counteract chemotherapy-induced neuropathic pain |
title_full_unstemmed | DF2726A, a new IL-8 signalling inhibitor, is able to counteract chemotherapy-induced neuropathic pain |
title_short | DF2726A, a new IL-8 signalling inhibitor, is able to counteract chemotherapy-induced neuropathic pain |
title_sort | df2726a, a new il-8 signalling inhibitor, is able to counteract chemotherapy-induced neuropathic pain |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6692352/ https://www.ncbi.nlm.nih.gov/pubmed/31409858 http://dx.doi.org/10.1038/s41598-019-48231-z |
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