Across CCLE and GDSC cell-line panels, response to BAY-HDAC11_4 is significantly associated with the pathway activity of multiple pathways, with PANCREAS cell lines showing a particularly strong set of associations.
The most reproducible BAY-HDAC11_4 response-associated pathways across cancer lineages are Negative regulation of nuclear-transcribed mRNA catabolic process, nonsense-mediated decay, Host-mediated suppression of viral transcription, and Host-mediated suppression of viral proces, each associated with drug response in up to 9 lineages. Since the analysis identifies associations rather than directional relationships, both response-to-biomarker and biomarker-to-response views are provided.
Each biomarker is linked to its corresponding Q-omics profile. The scatter plot shows the strongest observed association, BAY-HDAC11_4 response versus Negative regulation of nuclear-transcribed mRNA catabolic process, nonsense-mediated decay pathway activity in PANCREAS (Pearson r = 0.67).