Ontology highlight
ABSTRACT: This study aims to investigate the metabolic alterations associated with acquired tamoxifen (TAM) resistance in luminal A breast cancer cells. Using untargeted LC-MS/MS metabolomics, we compared parental MCF7 and TAM-resistant MCF7/Tam1 cells to identify key metabolic pathways affected by EPAS1 (HIF-2α)-mediated hypoxia-driven reprogramming. The study further evaluates the impact of EPAS1 inhibition by PT2977 on the reversal of these metabolic changes and restoration of TAM sensitivity.
INSTRUMENT(S): Liquid Chromatography MS -
PROVIDER: MTBLS12677 | MetaboLights | 2025-07-04
REPOSITORIES: MetaboLights
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| a_MTBLS12677_LC-MS___metabolite_profiling.txt | Txt | |||
| i_Investigation.txt | Txt | |||
| m_MTBLS12677_LC-MS___metabolite_profiling_v2_maf.tsv | Tabular | |||
| s_MTBLS12677.txt | Txt |
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