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Zinc complex of 3,5-di-tert-butyl salicylate inhibits viability, migration, and invasion in triple-negative breast cancer cells
The zinc complex of 3,5-di-tert-butyl salicylate (Zn{[CH(3))(3)C](2)Sal}(2)(2−)) is a zinc ion chelate of salicylate. In this study, we found that this compound inhibits viability, invasion, and migration and induces apoptosis in triple-negative breast cancer 4T1 cells. RNA-seq showed that the expre...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8927491/ https://www.ncbi.nlm.nih.gov/pubmed/35296801 http://dx.doi.org/10.1038/s41598-022-08704-0 |
Sumario: | The zinc complex of 3,5-di-tert-butyl salicylate (Zn{[CH(3))(3)C](2)Sal}(2)(2−)) is a zinc ion chelate of salicylate. In this study, we found that this compound inhibits viability, invasion, and migration and induces apoptosis in triple-negative breast cancer 4T1 cells. RNA-seq showed that the expression of 17 genes was upregulated and 26 genes were downregulated significantly by Zn{[CH(3))(3)C](2)Sal}(2)(2−) treatment. Further GO and KEGG analysis showed that the activity of Zn{[CH(3))(3)C](2)Sal}(2)(2−) against triple-negative breast cancer cells may be involved in the JAK-STAT3, HIF-1, and TNF signaling pathways. The expression of key genes was verified by RT–PCR. The phosphorylation of STAT3 and its upstream SRC decreased drastically upon Zn{[CH(3))(3)C](2)Sal}(2)(2−) treatment, as demonstrated by western blot. Our results indicate that Zn{[CH(3))(3)C](2)Sal}(2)(2−) inhibits the activity of TNBC cells by downregulating the STAT3 signaling through the SRC pathway. |
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