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Inhibition of Tumor Growth and Modulation of Antioxidant Activity of Rhodoxanthin Isolated from ITaxus baccata/I 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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Bibliographic Details
Published in:Antioxidants 2022-11, Vol.11 (11)
Main Authors: Dumitraş, Daria-Antonia, Dreanca, Alexandra Iulia, Pall, Emoke, Gal, Adrian Florin, Rus, Vasile, Morohoschi, Andreea Georgiana, Cotul, Mihaela, Nan, Monica Irina, Andrei, Sanda
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Language:English
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Summary: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[sup.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.
ISSN:2076-3921
2076-3921
DOI:10.3390/antiox11112264