Q-omics provides the consensus-scored MIR215 profile across patient tissues and cancer cell-line models. MIR215 expression is associated with patient survival in 14 of 34 cancer types, with the highest sampling consensus in ACC. Among the 18 cancer types available for tumor–normal comparison, MIR215 is differentially expressed in 5, with the highest sampling consensus in COAD. Additionally, MIR215 RNA expression shows 11,852 significant protein co-abundance associations, with the highest sampling consensus in LSCC. Together, these results highlight ACC, COAD, and LSCC as cancer lineages where MIR215 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 MIR215 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes MIR215 survival associations across molecular data types. MIR215 RNA expression shows survival associations in the most cancer types (14). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible MIR215 RNA expression–survival associations across cancer types. High MIR215 expression shows unfavorable associations in ACC, HNSC, SKCM, ESCA and THCA, but favorable associations in KIRP. The ACC Kaplan–Meier curve shows clear separation, with the high-expression group declining faster, consistent with the unfavorable association (log-rank p = .001). Together, the overview and detailed table identify ACC as the clearest survival context for MIR215 RNA expression.
This table summarizes MIR215 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 COAD for RNA.
This table ranks reproducible tumor–normal expression differences for MIR215. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. MIR215 shows lower tumor expression in COAD and LUAD and higher tumor expression in PRAD, HNSC and LIHC. The COAD box plot shows higher MIR215 RNA expression in normal versus tumor tissue (log2 FC = −0.996, t-test p < 0.001).
This table shows molecular features associated with MIR215 in patient tissues and cancer cell lines. In patient samples, MIR215 shows the broadest associations at the RNA and protein expression levels, with LSCC recurring as the lineage with the largest associated feature set.
