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Astaxanthin suppresses the metastasis of clear cell renal cell carcinoma through ROS scavenging
[Display omitted] •Astaxanthin blocks epithelial-mesenchymal transition of ccRCC cells.•Astaxanthin attenuates migratory and invasive activity of ccRCC cells.•The in vivo metastatic potential of ccRCC cells is suppressed by Astaxanthin.•Astaxanthin shows anti-metastatic activity through its ROS-scav...
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Published in: | Journal of functional foods 2024-05, Vol.116, p.106139, Article 106139 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
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Summary: | [Display omitted]
•Astaxanthin blocks epithelial-mesenchymal transition of ccRCC cells.•Astaxanthin attenuates migratory and invasive activity of ccRCC cells.•The in vivo metastatic potential of ccRCC cells is suppressed by Astaxanthin.•Astaxanthin shows anti-metastatic activity through its ROS-scavenging capacity.
Clear cell renal cell carcinoma (ccRCC) represents a prevalent form of kidney cancer, and its poor prognosis is closely tied to the occurrence of metastasis. ROS can drive epithelial-mesenchymal transition (EMT), thereby promoting cancer metastasis. Astaxanthin (AXT), renowned for its exceptional antioxidant properties, has been shown in this study to suppress ccRCC metastasis by scavenging ROS. AXT dose-dependently reduced ROS levels and attenuated migratory and invasive capabilities of ccRCC cells. Additionally, ccRCC cells treated with AXT exhibited phenotypic characteristics indicating EMT inhibition, which was reflected by the increased E-cadherin and decreased vimentin. Furthermore, AXT-induced suppressed metastatic potential was also corroborated in mouse lung metastasis model. Notably, artificially elevating ROS levels reversed the AXT-induced reduction in migratory and invasive capacity. Taken together, these findings highlight the anti-metastatic function of AXT in ccRCC, suggesting its therapeutic potential in the management of ccRCC metastasis. |
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ISSN: | 1756-4646 2214-9414 |
DOI: | 10.1016/j.jff.2024.106139 |