Q-omics provides the consensus-scored MIR1972-2 profile across patient tissues and cancer cell-line models. MIR1972-2 expression is associated with patient survival in 11 of 34 cancer types, with the highest sampling consensus in PAAD. Among the 18 cancer types available for tumor–normal comparison, MIR1972-2 is differentially expressed in 7, with the highest sampling consensus in STAD. Additionally, MIR1972-2 RNA expression shows 6,251 significant pathway-activity associations, with the highest sampling consensus in STAD. Together, these results highlight PAAD, and STAD as cancer lineages where MIR1972-2 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 MIR1972-2 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes MIR1972-2 survival associations across molecular data types. MIR1972-2 RNA expression shows survival associations in the most cancer types (11). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible MIR1972-2 RNA expression–survival associations across cancer types. High MIR1972-2 expression shows unfavorable associations in PAAD, THCA, KICH and SKCM, but favorable associations in LUAD and BLCA. The PAAD Kaplan–Meier curve shows clear separation, with the high-expression group declining faster, consistent with the unfavorable association (log-rank p = .003). Together, the overview and detailed table identify PAAD as the clearest survival context for MIR1972-2 RNA expression.
This table summarizes MIR1972-2 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 7. The strongest signals are observed in STAD for RNA.
This table ranks reproducible tumor–normal expression differences for MIR1972-2. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. MIR1972-2 shows lower tumor expression in LUSC, PAAD, KIRP and KIRC and higher tumor expression in STAD and UCEC. The STAD box plot shows higher MIR1972-2 RNA expression in tumor versus normal tissue (log2 FC = +0.860, t-test p = .002).
This table shows molecular features associated with MIR1972-2 in patient tissues and cancer cell lines. In patient samples, MIR1972-2 shows the broadest associations at the RNA and protein expression levels, with STAD recurring as the lineage with the largest associated feature set.
