Q-omics provides the consensus-scored MIR569 profile across patient tissues and cancer cell-line models. MIR569 expression is associated with patient survival in 9 of 34 cancer types, with the highest sampling consensus in READ. Among the 18 cancer types available for tumor–normal comparison, MIR569 is differentially expressed in 6, with the highest sampling consensus in KIRP. Additionally, MIR569 RNA expression shows 12,132 significant gene co-expression associations, with the highest sampling consensus in ESCA. Together, these results highlight READ, KIRP, and ESCA as cancer lineages where MIR569 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 MIR569 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes MIR569 survival associations across molecular data types. MIR569 RNA expression shows survival associations in the most cancer types (9). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible MIR569 RNA expression–survival associations across cancer types. High MIR569 expression shows unfavorable associations in READ, UCEC, BLCA and STAD, but favorable associations in KIRC and CHOL. The READ 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 READ as the clearest survival context for MIR569 RNA expression.
This table summarizes MIR569 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 6. The strongest signals are observed in KIRP for RNA.
This table ranks reproducible tumor–normal expression differences for MIR569. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. MIR569 shows higher tumor expression in KIRP, STAD, BRCA, LUAD, THCA and LUSC. The KIRP box plot shows higher MIR569 RNA expression in tumor versus normal tissue (log2 FC = +0.389, t-test p = .011).
This table shows molecular features associated with MIR569 in patient tissues and cancer cell lines. In patient samples, MIR569 shows the broadest associations at the RNA and protein expression levels, with ESCA recurring as the lineage with the largest associated feature set.
