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A Drosophila model relevant to chemotherapy-related cognitive impairment
Chemotherapy-related cognitive impairment (CRCI) is a common adverse effect of treatment and is characterized by deficits involving multiple cognitive domains including memory. Despite the significant morbidity of CRCI and the expected increase in cancer survivors over the coming decades, the pathop...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10630312/ https://www.ncbi.nlm.nih.gov/pubmed/37935827 http://dx.doi.org/10.1038/s41598-023-46616-9 |
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author | Torre, Matthew Bukhari, Hassan Nithianandam, Vanitha Zanella, Camila A. Mata, Douglas A. Feany, Mel B. |
author_facet | Torre, Matthew Bukhari, Hassan Nithianandam, Vanitha Zanella, Camila A. Mata, Douglas A. Feany, Mel B. |
author_sort | Torre, Matthew |
collection | PubMed |
description | Chemotherapy-related cognitive impairment (CRCI) is a common adverse effect of treatment and is characterized by deficits involving multiple cognitive domains including memory. Despite the significant morbidity of CRCI and the expected increase in cancer survivors over the coming decades, the pathophysiology of CRCI remains incompletely understood, highlighting the need for new model systems to study CRCI. Given the powerful array of genetic approaches and facile high throughput screening ability in Drosophila, our goal was to validate a Drosophila model relevant to CRCI. We administered the chemotherapeutic agents cisplatin, cyclophosphamide, and doxorubicin to adult Drosophila. Neurologic deficits were observed with all tested chemotherapies, with doxorubicin and in particular cisplatin also resulting in memory deficits. We then performed histologic and immunohistochemical analysis of cisplatin-treated Drosophila tissue, demonstrating neuropathologic evidence of increased neurodegeneration, DNA damage, and oxidative stress. Thus, our Drosophila model relevant to CRCI recapitulates clinical, radiologic, and histologic alterations reported in chemotherapy patients. Our new Drosophila model can be used for mechanistic dissection of pathways contributing to CRCI (and chemotherapy-induced neurotoxicity more generally) and pharmacologic screens to identify disease-modifying therapies. |
format | Online Article Text |
id | pubmed-10630312 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-106303122023-11-07 A Drosophila model relevant to chemotherapy-related cognitive impairment Torre, Matthew Bukhari, Hassan Nithianandam, Vanitha Zanella, Camila A. Mata, Douglas A. Feany, Mel B. Sci Rep Article Chemotherapy-related cognitive impairment (CRCI) is a common adverse effect of treatment and is characterized by deficits involving multiple cognitive domains including memory. Despite the significant morbidity of CRCI and the expected increase in cancer survivors over the coming decades, the pathophysiology of CRCI remains incompletely understood, highlighting the need for new model systems to study CRCI. Given the powerful array of genetic approaches and facile high throughput screening ability in Drosophila, our goal was to validate a Drosophila model relevant to CRCI. We administered the chemotherapeutic agents cisplatin, cyclophosphamide, and doxorubicin to adult Drosophila. Neurologic deficits were observed with all tested chemotherapies, with doxorubicin and in particular cisplatin also resulting in memory deficits. We then performed histologic and immunohistochemical analysis of cisplatin-treated Drosophila tissue, demonstrating neuropathologic evidence of increased neurodegeneration, DNA damage, and oxidative stress. Thus, our Drosophila model relevant to CRCI recapitulates clinical, radiologic, and histologic alterations reported in chemotherapy patients. Our new Drosophila model can be used for mechanistic dissection of pathways contributing to CRCI (and chemotherapy-induced neurotoxicity more generally) and pharmacologic screens to identify disease-modifying therapies. Nature Publishing Group UK 2023-11-07 /pmc/articles/PMC10630312/ /pubmed/37935827 http://dx.doi.org/10.1038/s41598-023-46616-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Torre, Matthew Bukhari, Hassan Nithianandam, Vanitha Zanella, Camila A. Mata, Douglas A. Feany, Mel B. A Drosophila model relevant to chemotherapy-related cognitive impairment |
title | A Drosophila model relevant to chemotherapy-related cognitive impairment |
title_full | A Drosophila model relevant to chemotherapy-related cognitive impairment |
title_fullStr | A Drosophila model relevant to chemotherapy-related cognitive impairment |
title_full_unstemmed | A Drosophila model relevant to chemotherapy-related cognitive impairment |
title_short | A Drosophila model relevant to chemotherapy-related cognitive impairment |
title_sort | drosophila model relevant to chemotherapy-related cognitive impairment |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10630312/ https://www.ncbi.nlm.nih.gov/pubmed/37935827 http://dx.doi.org/10.1038/s41598-023-46616-9 |
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