Q-omics provides the consensus-scored RB1-DT profile across patient tissues and cancer cell-line models. RB1-DT expression is associated with patient survival in 22 of 34 cancer types, with the highest sampling consensus in LUAD. Among the 18 cancer types available for tumor–normal comparison, RB1-DT is differentially expressed in 5, with the highest sampling consensus in THCA. Additionally, RB1-DT RNA expression shows 17,205 significant gene co-expression associations, with the highest sampling consensus in UVM. Together, these results highlight LUAD, THCA, and UVM as cancer lineages where RB1-DT 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 RB1-DT — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes RB1-DT survival associations across molecular data types. RB1-DT 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 RB1-DT RNA expression–survival associations across cancer types. High RB1-DT expression shows unfavorable associations in KICH and HNSC, but favorable associations in LUAD, UCS, READ and BRCA. The LUAD Kaplan–Meier curve shows clear separation, with the low-expression group declining faster, consistent with the favorable association (log-rank p < 0.001). Together, the overview and detailed table identify LUAD as the clearest survival context for RB1-DT RNA expression.
This table summarizes RB1-DT tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 5. The strongest signals are observed in THCA for RNA.
This table ranks reproducible tumor–normal expression differences for RB1-DT. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. RB1-DT shows lower tumor expression in THCA, KICH and BRCA and higher tumor expression in COAD and STAD. The THCA box plot shows higher RB1-DT RNA expression in normal versus tumor tissue (log2 FC = −0.438, t-test p < 0.001).
This table shows molecular features associated with RB1-DT in patient tissues and cancer cell lines. In patient samples, RB1-DT shows the broadest associations at the RNA and protein expression levels, with UVM recurring as the lineage with the largest associated feature set.
