Q-omics provides the consensus-scored RUNX3-AS1 profile across patient tissues and cancer cell-line models. RUNX3-AS1 expression is associated with patient survival in 22 of 34 cancer types, with the highest sampling consensus in ACC. Among the 18 cancer types available for tumor–normal comparison, RUNX3-AS1 is differentially expressed in 9, with the highest sampling consensus in HNSC. Additionally, RUNX3-AS1 RNA expression shows 14,691 significant gene co-expression associations, with the highest sampling consensus in DLBC. Together, these results highlight ACC, HNSC, and DLBC as cancer lineages where RUNX3-AS1 shows reproducible signals across survival, tumor–normal expression, and patient cross-omics 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.
Premium analyses for RUNX3-AS1 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes RUNX3-AS1 survival associations across molecular data types. RUNX3-AS1 RNA expression shows survival associations in the most cancer types (22). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible RUNX3-AS1 RNA expression–survival associations across cancer types. High RUNX3-AS1 expression shows unfavorable associations in ACC, KIRC, THCA, LGG and UCS, but favorable associations in CESC. The ACC Kaplan–Meier curve shows clear separation, with the high-expression group declining faster, consistent with the unfavorable association (log-rank p < 0.001). Together, the overview and detailed table identify ACC as the clearest survival context for RUNX3-AS1 RNA expression.
This table summarizes RUNX3-AS1 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 9. The strongest signals are observed in HNSC for RNA.
This table ranks reproducible tumor–normal expression differences for RUNX3-AS1. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. RUNX3-AS1 shows lower tumor expression in BRCA and higher tumor expression in HNSC, KIRC, LUAD, LUSC and STAD. The HNSC box plot shows higher RUNX3-AS1 RNA expression in tumor versus normal tissue (log2 FC = +0.403, t-test p < 0.001).
This table shows molecular features associated with RUNX3-AS1 in patient tissues and cancer cell lines. In patient samples, RUNX3-AS1 shows the broadest associations at the RNA and protein expression levels, with DLBC recurring as the lineage with the largest associated feature set.
