GO:0043501Ontology (GO BP)GO biological process · ~25 member genes
Q-omics provides the Skeletal muscle adaptation (GO:0043501) pathway profile, scoring each patient from the combined activity of its roughly 25 member genes. Pathway activity is associated with patient survival in 21 of 34 cancer types, with the highest sampling consensus in CHOL. Among the 18 cancer types available for tumor–normal comparison, the pathway is differentially active in 8, with the highest sampling consensus in THCA. Additionally, pathway RNA activity shows 26,607 significant cross-omics associations, again with the highest sampling consensus in BRCA. Together, these results highlight CHOL, THCA, and BRCA as cancer lineages where the pathway shows reproducible signals across outcome, tissue activity, and molecular association analyses.
Every result is evaluated using two consensus scores. Sampling consensus measures how consistently a finding is reproduced within a cancer lineage across different conditions. Lineage consensus measures how broadly the result is shared across cancer types, distinguishing pan-cancer signals from lineage-specific patterns. Pathway-against-pathway and pathway-against-mutation comparisons are not available for ontology entities.
Survival associations
This table summarizes Skeletal muscle adaptation survival associations by molecular data type. RNA-level pathway activity shows survival associations in the most cancer types (21). The rightmost column indicates the cancer type with the highest sampling consensus for each layer.
This table ranks reproducible pathway activity–survival associations across cancer types. High Skeletal muscle adaptation activity shows favorable associations in BLCA, but unfavorable associations in CHOL, MESO, PAAD, THYM and STAD. In the CHOL Kaplan–Meier curve the high-activity group declines faster, consistent with the unfavorable association (log-rank p < 0.001). CHOL ranks highest by sampling consensus for Skeletal muscle adaptation.
This table summarizes Skeletal muscle adaptation tumor–normal activity differences by data type. RNA-level activity shows significant tumor–normal differences in 8 cancer types, while mass-spec protein activity shows differences in 5. The strongest signals are in THCA for RNA and COAD for protein.
This table ranks reproducible tumor–normal activity differences for the pathway. A positive fold-change indicates higher activity in tumor tissue. The pathway shows higher tumor activity across COAD, KIRP, CHOL, BRCA and LIHC and lower tumor activity in THCA. In the THCA box plot, normal samples show higher pathway activity than tumor samples (log2 FC = −0.125, t-test p < 0.001).
This table shows molecular features associated with Skeletal muscle adaptation pathway activity in patient tissues and cancer cell lines. In patient samples, pathway activity is most strongly linked to RNA and protein features, with the largest associated set in BRCA. In cancer cell lines, RNA-expression features and functional dependencies dominate, with the largest set in OESOPHAGUS.
