GO:0072162Ontology (GO BP)GO biological process · ~5 member genes
Q-omics provides the Metanephric mesenchymal cell differentiation (GO:0072162) pathway profile, scoring each patient from the combined activity of its roughly 5 member genes. Pathway activity is associated with patient survival in 21 of 34 cancer types, with the highest sampling consensus in OV. Among the 18 cancer types available for tumor–normal comparison, the pathway is differentially active in 12, with the highest sampling consensus in THCA. Additionally, pathway RNA activity shows 30,580 significant cross-omics associations, again with the highest sampling consensus in THCA. Together, these results highlight OV, and THCA 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 Metanephric mesenchymal cell differentiation 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 Metanephric mesenchymal cell differentiation activity shows favorable associations in OV, READ, SKCM, PAAD and KIRP, but unfavorable associations in ACC. In the OV Kaplan–Meier curve the low-activity group declines faster, consistent with the favorable association (log-rank p < 0.001). OV ranks highest by sampling consensus for Metanephric mesenchymal cell differentiation.
This table summarizes Metanephric mesenchymal cell differentiation tumor–normal activity differences by data type. RNA-level activity shows significant tumor–normal differences in 12 cancer types, while mass-spec protein activity shows differences in 5. The strongest signals are in BLCA for RNA and PDAC 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 THCA and LIHC and lower tumor activity in BLCA, KIRP, KIRC and LUSC. In the THCA box plot, tumor samples show higher pathway activity than matched normal samples (log2 FC = +0.331, t-test p < 0.001).
This table shows molecular features associated with Metanephric mesenchymal cell differentiation 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 THCA. In cancer cell lines, RNA-expression features and functional dependencies dominate, with the largest set in LUNG_NSCLC_LUSC.
