Whey Protein Concentrate Renders MDA-MB-231 Cells Sensitive to Rapamycin by Altering Cellular Redox State and Activating GSK3β/mTOR Signaling
Autor: | Yang-Ming Tseng, Li-Yu Tsai, Szu-Hsien Wu, Shih-Meng Tsai, Shih-Hsuan Cheng |
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Jazyk: | angličtina |
Rok vydání: | 2017 |
Předmět: |
0301 basic medicine
Whey protein Regulator lcsh:Medicine Models Biological Article 03 medical and health sciences chemistry.chemical_compound Cell Line Tumor Humans lcsh:Science Tumor Stem Cell Assay PI3K/AKT/mTOR pathway Cell Nucleus Sirolimus chemistry.chemical_classification Reactive oxygen species Glycogen Synthase Kinase 3 beta Multidisciplinary Chemistry TOR Serine-Threonine Kinases lcsh:R Glutathione Neoplasm Proteins Cell biology Whey Proteins 030104 developmental biology Biochemistry Cell culture Cancer cell lcsh:Q Oxidation-Reduction Signal Transduction |
Zdroj: | Scientific Reports, Vol 7, Iss 1, Pp 1-11 (2017) Scientific Reports |
ISSN: | 2045-2322 |
DOI: | 10.1038/s41598-017-14159-5 |
Popis: | Whey protein concentrate (WPC) is an amino acid-rich supplement that has been shown to increase cellular antioxidant capacity. Mammalian target of rapamycin (mTOR) is a crucial regulator of signaling in mammalian cells, and serves as a therapeutic target for triple-negative breast cancer (TNBC). This study was designed to investigate the effect of combining WPC with rapamycin on MDA-MB-231 human breast cancer cells. These cells were found to be insensitive to rapamycin and exhibited higher glutathione (GSH) and reactive oxygen species levels than non-tumorigenic MCF-10A cells. However, for MDA-MB-231 cells, the half maximal inhibitory concentration of rapamycin was lower when this drug was administered in combination with WPC than when used alone. Furthermore, combining WPC with rapamycin depleted GSH levels and reduced Nrf2 nuclear accumulation. In addition, WPC activated GSK3β/mTOR signaling, and GSK3β appeared to be involved in the WPC-mediated Nrf2 reduction and mTOR activation. In conclusion, WPC induced rapamycin sensitivity in MDA-MB-231 cells by altering their redox state and activating GSK3β/mTOR signaling. These results not only suggest a novel therapeutic approach for breast cancer treatment, but also provide insight into the critical pathways affecting the resistance to mTOR inhibition observed in a subgroup of TNBC patients. |
Databáze: | OpenAIRE |
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