Across TCGA patient cohorts, RNA activity of the "Regulation of nuclear-transcribed mRNA catabolic process, deadenylation-dependent decay" pathway is significantly associated with the protein abundance of multiple proteins, with the HNSC cohort showing a particularly strong set of associations.
The most reproducible pathway-associated proteins across cancer lineages are RPL26, GALNT7, and COPB1, each associated with the pathway in up to 5 cancer types. Since the analysis shows associations rather than directional relationships, both pathway-to-partner and partner-to-pathway views are reported.
Each partner is linked to its corresponding Q-omics profile. The scatter plot shows the strongest association, "Regulation of nuclear-transcribed mRNA catabolic process, deadenylation-dependent decay" activity versus RPL26 in HNSC (Pearson r = -0.35).