Insights into cisplatin-induced neurotoxicity and mitochondrial dysfunction in Caenorhabditis elegans

Cisplatin is the most common drug in first-line chemotherapy against solid tumors. We and others have previously used the nematode Caenorhabditis elegans to identify genetic factors influencing the sensitivity and resistance to cisplatin. In this study, we used C. elegans to explore cisplatin effect...

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Main Authors: Carmen Martínez-Fernández (Author), Milana Bergamino (Author), Alfonso Schiavi (Author), David Brena (Author), Natascia Ventura (Author), Sebastian Honnen (Author), Alberto Villanueva (Author), Ernest Nadal (Author), Julián Cerón (Author)
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Published: The Company of Biologists, 2022-03-01T00:00:00Z.
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100 1 0 |a Carmen Martínez-Fernández  |e author 
700 1 0 |a Milana Bergamino  |e author 
700 1 0 |a Alfonso Schiavi  |e author 
700 1 0 |a David Brena  |e author 
700 1 0 |a Natascia Ventura  |e author 
700 1 0 |a Sebastian Honnen  |e author 
700 1 0 |a Alberto Villanueva  |e author 
700 1 0 |a Ernest Nadal  |e author 
700 1 0 |a Julián Cerón  |e author 
245 0 0 |a Insights into cisplatin-induced neurotoxicity and mitochondrial dysfunction in Caenorhabditis elegans 
260 |b The Company of Biologists,   |c 2022-03-01T00:00:00Z. 
500 |a 1754-8403 
500 |a 1754-8411 
500 |a 10.1242/dmm.049161 
520 |a Cisplatin is the most common drug in first-line chemotherapy against solid tumors. We and others have previously used the nematode Caenorhabditis elegans to identify genetic factors influencing the sensitivity and resistance to cisplatin. In this study, we used C. elegans to explore cisplatin effects on mitochondrial functions and investigate cisplatin-induced neurotoxicity through a high-resolution system for evaluating locomotion. First, we report that a high-glucose diet sensitizes C. elegans to cisplatin at the physiological level and that mitochondrial CED-13 protects the cell from cisplatin-induced oxidative stress. Additionally, by assessing mitochondrial function with a Seahorse XFe96 Analyzer, we observed a detrimental effect of cisplatin and glucose on mitochondrial respiration. Second, because catechol-O-methyltransferases (involved in dopamine degradation) are upregulated upon cisplatin exposure, we studied the protective role of dopamine against cisplatin-induced neurotoxicity. Using a Tierpsy Tracker system for measuring neurotoxicity, we showed that abnormal displacements and body postures in cat-2 mutants, which have dopamine synthesis disrupted, can be rescued by adding dopamine. Then, we demonstrated that dopamine treatment protects against the dose-dependent neurotoxicity caused by cisplatin. 
546 |a EN 
690 |a c. elegans 
690 |a crispr-cas9 
690 |a cisplatin 
690 |a glucose 
690 |a mitochondria 
690 |a neurotoxicity 
690 |a Medicine 
690 |a R 
690 |a Pathology 
690 |a RB1-214 
655 7 |a article  |2 local 
786 0 |n Disease Models & Mechanisms, Vol 15, Iss 3 (2022) 
787 0 |n http://dmm.biologists.org/content/15/3/dmm049161 
787 0 |n https://doaj.org/toc/1754-8403 
787 0 |n https://doaj.org/toc/1754-8411 
856 4 1 |u https://doaj.org/article/cdcb1c8b76c94909a5a92b8767d40b32  |z Connect to this object online.