fig5

Divergent transcriptional programs and constrained metabolic states reveal selective metabolic dependencies in chemoresistant luminal breast cancer

Figure 5. Metabolomic profiling reveals limited global divergence but identifies selective metabolic alterations in chemoresistant HR+/HER2- BC cells. (A) Integrated transcriptomic and metabolomic pathway enrichment analysis highlighting dysregulated metabolic pathways in taxane- and anthracycline-resistant models; (B and C) Heatmaps of the top 50 most regulated metabolites in chemoresistant MCF-7 (B) and ZR-75-1 (C) cell models relative to their parental counterparts. Color scale represents log10-transformed intensities. HR+/HER2-: Hormone receptor-positive/human epidermal growth factor receptor 2-negative; BC: breast cancer; NES: normalized enrichment score; Pac-R: paclitaxel-resistant; Epi-R: epirubicin-resistant; Doc-R: docetaxel-resistant.

Cancer Drug Resistance
ISSN 2578-532X (Online)

Portico

All published articles will preserved here permanently:

https://www.portico.org/publishers/oae/

Portico

All published articles will preserved here permanently:

https://www.portico.org/publishers/oae/