Across TCGA patient cohorts, RNA activity of the Negative regulation of post-transcriptional gene silencing 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 VDAC2_T68, IDE, and PGAM1_S31, each associated with the pathway in up to 4 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, Negative regulation of post-transcriptional gene silencing activity versus VDAC2_T68 in HNSC (Pearson r = -0.13).