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Curcumin Acts as a Chemosensitizer for Leiomyosarcoma Cells In Vitro But Fails to Mediate Antioxidant Enzyme Activity in Cisplatin-Induced Experimental Nephrotoxicity in Rats

Background. Cisplatin (cis-diamminedichloroplatinum) is a widely used chemotherapeutic agent for the treatment of various cancers. Although it represents an effective regimen, its application is accompanied by side effects to normal tissues, especially to the kidneys. Cisplatin generates free radica...

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Autores principales: Dhima, Irida, Zerikiotis, Stelios, Lekkas, Panagiotis, Simos, Yannis V., Gkiouli, Maria, Vezyraki, Patra, Dounousi, Evangelia, Ragos, Vasilios, Giannakopoulos, Xenophon, Baltogiannis, Dimitrios, Kalfakakou, Vasiliki, Evangelou, Angelos, Peschos, Dimitrios, Karkabounas, Spyridon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6710690/
https://www.ncbi.nlm.nih.gov/pubmed/31441361
http://dx.doi.org/10.1177/1534735419872811
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author Dhima, Irida
Zerikiotis, Stelios
Lekkas, Panagiotis
Simos, Yannis V.
Gkiouli, Maria
Vezyraki, Patra
Dounousi, Evangelia
Ragos, Vasilios
Giannakopoulos, Xenophon
Baltogiannis, Dimitrios
Kalfakakou, Vasiliki
Evangelou, Angelos
Peschos, Dimitrios
Karkabounas, Spyridon
author_facet Dhima, Irida
Zerikiotis, Stelios
Lekkas, Panagiotis
Simos, Yannis V.
Gkiouli, Maria
Vezyraki, Patra
Dounousi, Evangelia
Ragos, Vasilios
Giannakopoulos, Xenophon
Baltogiannis, Dimitrios
Kalfakakou, Vasiliki
Evangelou, Angelos
Peschos, Dimitrios
Karkabounas, Spyridon
author_sort Dhima, Irida
collection PubMed
description Background. Cisplatin (cis-diamminedichloroplatinum) is a widely used chemotherapeutic agent for the treatment of various cancers. Although it represents an effective regimen, its application is accompanied by side effects to normal tissues, especially to the kidneys. Cisplatin generates free radicals and impairs the function of antioxidant enzymes. Modulation of cisplatin-induced oxidative stress by specific antioxidant molecules represents an attractive approach to minimize side effects. Methods. We studied the ability of curcumin to sensitize leiomyosarcoma (LMS) cells to cisplatin. Assays for cell proliferation, mitochondrial function, induction of apoptosis, and cell cycle arrest were performed using various concentrations of cisplatin and a concentration of curcumin that caused a nonsignificant reduction in cell viability. Moreover, the effect of curcumin was examined against cisplatin-induced experimental nephrotoxicity. Renal injury was assessed by measuring serum creatinine, blood urea nitrogen (BUN), and the kidney’s relative weight. Oxidative stress was measured by means of enzymatic activities of superoxide dismutase and glutathione peroxidase in the rats’ blood and malondialdehyde levels in rats’ urine. Results. In our study, we found that curcumin sensitizes LMS cells to cisplatin by enhancing apoptosis and impairing mitochondrial function. In an in vivo model of cisplatin-induced experimental nephrotoxicity, intraperitoneal administration of curcumin failed to preserve blood’s antioxidant enzyme activity and decrease lipid peroxidation. Nevertheless, curcumin was able to protect nephrons’ histology from cisplatin’s toxic effect. Conclusion. Our results showed that curcumin can act as chemosensitizer, but its role as an adjunctive cisplatin-induced oxidative stress inhibitor requires further dose-finding studies to maximize the effectiveness of chemotherapy.
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spelling pubmed-67106902019-09-05 Curcumin Acts as a Chemosensitizer for Leiomyosarcoma Cells In Vitro But Fails to Mediate Antioxidant Enzyme Activity in Cisplatin-Induced Experimental Nephrotoxicity in Rats Dhima, Irida Zerikiotis, Stelios Lekkas, Panagiotis Simos, Yannis V. Gkiouli, Maria Vezyraki, Patra Dounousi, Evangelia Ragos, Vasilios Giannakopoulos, Xenophon Baltogiannis, Dimitrios Kalfakakou, Vasiliki Evangelou, Angelos Peschos, Dimitrios Karkabounas, Spyridon Integr Cancer Ther Research Articles Background. Cisplatin (cis-diamminedichloroplatinum) is a widely used chemotherapeutic agent for the treatment of various cancers. Although it represents an effective regimen, its application is accompanied by side effects to normal tissues, especially to the kidneys. Cisplatin generates free radicals and impairs the function of antioxidant enzymes. Modulation of cisplatin-induced oxidative stress by specific antioxidant molecules represents an attractive approach to minimize side effects. Methods. We studied the ability of curcumin to sensitize leiomyosarcoma (LMS) cells to cisplatin. Assays for cell proliferation, mitochondrial function, induction of apoptosis, and cell cycle arrest were performed using various concentrations of cisplatin and a concentration of curcumin that caused a nonsignificant reduction in cell viability. Moreover, the effect of curcumin was examined against cisplatin-induced experimental nephrotoxicity. Renal injury was assessed by measuring serum creatinine, blood urea nitrogen (BUN), and the kidney’s relative weight. Oxidative stress was measured by means of enzymatic activities of superoxide dismutase and glutathione peroxidase in the rats’ blood and malondialdehyde levels in rats’ urine. Results. In our study, we found that curcumin sensitizes LMS cells to cisplatin by enhancing apoptosis and impairing mitochondrial function. In an in vivo model of cisplatin-induced experimental nephrotoxicity, intraperitoneal administration of curcumin failed to preserve blood’s antioxidant enzyme activity and decrease lipid peroxidation. Nevertheless, curcumin was able to protect nephrons’ histology from cisplatin’s toxic effect. Conclusion. Our results showed that curcumin can act as chemosensitizer, but its role as an adjunctive cisplatin-induced oxidative stress inhibitor requires further dose-finding studies to maximize the effectiveness of chemotherapy. SAGE Publications 2019-08-23 /pmc/articles/PMC6710690/ /pubmed/31441361 http://dx.doi.org/10.1177/1534735419872811 Text en © The Author(s) 2019 http://www.creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Research Articles
Dhima, Irida
Zerikiotis, Stelios
Lekkas, Panagiotis
Simos, Yannis V.
Gkiouli, Maria
Vezyraki, Patra
Dounousi, Evangelia
Ragos, Vasilios
Giannakopoulos, Xenophon
Baltogiannis, Dimitrios
Kalfakakou, Vasiliki
Evangelou, Angelos
Peschos, Dimitrios
Karkabounas, Spyridon
Curcumin Acts as a Chemosensitizer for Leiomyosarcoma Cells In Vitro But Fails to Mediate Antioxidant Enzyme Activity in Cisplatin-Induced Experimental Nephrotoxicity in Rats
title Curcumin Acts as a Chemosensitizer for Leiomyosarcoma Cells In Vitro But Fails to Mediate Antioxidant Enzyme Activity in Cisplatin-Induced Experimental Nephrotoxicity in Rats
title_full Curcumin Acts as a Chemosensitizer for Leiomyosarcoma Cells In Vitro But Fails to Mediate Antioxidant Enzyme Activity in Cisplatin-Induced Experimental Nephrotoxicity in Rats
title_fullStr Curcumin Acts as a Chemosensitizer for Leiomyosarcoma Cells In Vitro But Fails to Mediate Antioxidant Enzyme Activity in Cisplatin-Induced Experimental Nephrotoxicity in Rats
title_full_unstemmed Curcumin Acts as a Chemosensitizer for Leiomyosarcoma Cells In Vitro But Fails to Mediate Antioxidant Enzyme Activity in Cisplatin-Induced Experimental Nephrotoxicity in Rats
title_short Curcumin Acts as a Chemosensitizer for Leiomyosarcoma Cells In Vitro But Fails to Mediate Antioxidant Enzyme Activity in Cisplatin-Induced Experimental Nephrotoxicity in Rats
title_sort curcumin acts as a chemosensitizer for leiomyosarcoma cells in vitro but fails to mediate antioxidant enzyme activity in cisplatin-induced experimental nephrotoxicity in rats
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6710690/
https://www.ncbi.nlm.nih.gov/pubmed/31441361
http://dx.doi.org/10.1177/1534735419872811
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