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Inhibition of Tumor Growth and Modulation of Antioxidant Activity of Rhodoxanthin Isolated from Taxus baccata Aril against B16F10 Murine Malignant Melanoma

Malignant melanoma is the most aggressive type of skin cancer, and due to the numerous limitations of current treatment methods, there is an urgent need to develop novel approaches for both the prevention and treatment of malignant melanoma, with research-oriented bioactive substances representing a...

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Autores principales: Dumitraş, Daria-Antonia, Dreanca, Alexandra Iulia, Pall, Emoke, Gal, Adrian Florin, Rus, Vasile, Morohoschi, Andreea Georgiana, Cotul, Mihaela, Nan, Monica Irina, Andrei, Sanda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9687082/
https://www.ncbi.nlm.nih.gov/pubmed/36421450
http://dx.doi.org/10.3390/antiox11112264
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author Dumitraş, Daria-Antonia
Dreanca, Alexandra Iulia
Pall, Emoke
Gal, Adrian Florin
Rus, Vasile
Morohoschi, Andreea Georgiana
Cotul, Mihaela
Nan, Monica Irina
Andrei, Sanda
author_facet Dumitraş, Daria-Antonia
Dreanca, Alexandra Iulia
Pall, Emoke
Gal, Adrian Florin
Rus, Vasile
Morohoschi, Andreea Georgiana
Cotul, Mihaela
Nan, Monica Irina
Andrei, Sanda
author_sort Dumitraş, Daria-Antonia
collection PubMed
description Malignant melanoma is the most aggressive type of skin cancer, and due to the numerous limitations of current treatment methods, there is an urgent need to develop novel approaches for both the prevention and treatment of malignant melanoma, with research-oriented bioactive substances representing a notable first step. The current study decided to expand on previous rhodoxanthin research by investigating the possible anti-tumor effect as well as the effect on the antioxidant status in the case of murine melanoma in an experimental model. The 21-day study was carried out on female C57BL/6J mice. On the first day of the experiment, they were subcutaneously inoculated with 10(6) B16F10 cells and were given rhodoxanthin orally until the end of the study. Rhodoxanthin supplementation significantly reduced tumor growth (42.18%) and weight (15.74%). Furthermore, the epidermal growth factor (EGF) activity was reduced and the concentration of 8-OHdG dropped in the treated melanoma-bearing mice compared to the untreated ones, demonstrating the role of rhodoxanthin in slowing tumor growth, one of the mechanisms being the reduction of EGF level and the decrease of DNA oxidation. The administration of rhodoxanthin determined variations in antioxidant enzymes, both at the plasma level and at the tissue level.
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spelling pubmed-96870822022-11-25 Inhibition of Tumor Growth and Modulation of Antioxidant Activity of Rhodoxanthin Isolated from Taxus baccata Aril against B16F10 Murine Malignant Melanoma Dumitraş, Daria-Antonia Dreanca, Alexandra Iulia Pall, Emoke Gal, Adrian Florin Rus, Vasile Morohoschi, Andreea Georgiana Cotul, Mihaela Nan, Monica Irina Andrei, Sanda Antioxidants (Basel) Article Malignant melanoma is the most aggressive type of skin cancer, and due to the numerous limitations of current treatment methods, there is an urgent need to develop novel approaches for both the prevention and treatment of malignant melanoma, with research-oriented bioactive substances representing a notable first step. The current study decided to expand on previous rhodoxanthin research by investigating the possible anti-tumor effect as well as the effect on the antioxidant status in the case of murine melanoma in an experimental model. The 21-day study was carried out on female C57BL/6J mice. On the first day of the experiment, they were subcutaneously inoculated with 10(6) B16F10 cells and were given rhodoxanthin orally until the end of the study. Rhodoxanthin supplementation significantly reduced tumor growth (42.18%) and weight (15.74%). Furthermore, the epidermal growth factor (EGF) activity was reduced and the concentration of 8-OHdG dropped in the treated melanoma-bearing mice compared to the untreated ones, demonstrating the role of rhodoxanthin in slowing tumor growth, one of the mechanisms being the reduction of EGF level and the decrease of DNA oxidation. The administration of rhodoxanthin determined variations in antioxidant enzymes, both at the plasma level and at the tissue level. MDPI 2022-11-16 /pmc/articles/PMC9687082/ /pubmed/36421450 http://dx.doi.org/10.3390/antiox11112264 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Dumitraş, Daria-Antonia
Dreanca, Alexandra Iulia
Pall, Emoke
Gal, Adrian Florin
Rus, Vasile
Morohoschi, Andreea Georgiana
Cotul, Mihaela
Nan, Monica Irina
Andrei, Sanda
Inhibition of Tumor Growth and Modulation of Antioxidant Activity of Rhodoxanthin Isolated from Taxus baccata Aril against B16F10 Murine Malignant Melanoma
title Inhibition of Tumor Growth and Modulation of Antioxidant Activity of Rhodoxanthin Isolated from Taxus baccata Aril against B16F10 Murine Malignant Melanoma
title_full Inhibition of Tumor Growth and Modulation of Antioxidant Activity of Rhodoxanthin Isolated from Taxus baccata Aril against B16F10 Murine Malignant Melanoma
title_fullStr Inhibition of Tumor Growth and Modulation of Antioxidant Activity of Rhodoxanthin Isolated from Taxus baccata Aril against B16F10 Murine Malignant Melanoma
title_full_unstemmed Inhibition of Tumor Growth and Modulation of Antioxidant Activity of Rhodoxanthin Isolated from Taxus baccata Aril against B16F10 Murine Malignant Melanoma
title_short Inhibition of Tumor Growth and Modulation of Antioxidant Activity of Rhodoxanthin Isolated from Taxus baccata Aril against B16F10 Murine Malignant Melanoma
title_sort inhibition of tumor growth and modulation of antioxidant activity of rhodoxanthin isolated from taxus baccata aril against b16f10 murine malignant melanoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9687082/
https://www.ncbi.nlm.nih.gov/pubmed/36421450
http://dx.doi.org/10.3390/antiox11112264
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