Q-omics provides the consensus-scored PDE2A-AS1 profile across patient tissues and cancer cell-line models. PDE2A-AS1 expression is associated with patient survival in 20 of 34 cancer types, with the highest sampling consensus in UCS. Among the 18 cancer types available for tumor–normal comparison, PDE2A-AS1 is differentially expressed in 4, with the highest sampling consensus in KICH. Additionally, PDE2A-AS1 RNA expression shows 7,606 significant gene co-expression associations, with the highest sampling consensus in TGCT. Together, these results highlight UCS, KICH, and TGCT as cancer lineages where PDE2A-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 PDE2A-AS1 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes PDE2A-AS1 survival associations across molecular data types. PDE2A-AS1 RNA expression shows survival associations in the most cancer types (20). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible PDE2A-AS1 RNA expression–survival associations across cancer types. High PDE2A-AS1 expression shows unfavorable associations in UCS, UCEC, ACC, MESO, THYM and LUAD. The UCS Kaplan–Meier curve shows clear separation, with the high-expression group declining faster, consistent with the unfavorable association (log-rank p = .002). Together, the overview and detailed table identify UCS as the clearest survival context for PDE2A-AS1 RNA expression.
This table summarizes PDE2A-AS1 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 4. The strongest signals are observed in KICH for RNA.
This table ranks reproducible tumor–normal expression differences for PDE2A-AS1. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. PDE2A-AS1 shows lower tumor expression in LUSC, COAD and LUAD and higher tumor expression in KICH. The KICH box plot shows higher PDE2A-AS1 RNA expression in tumor versus normal tissue (log2 FC = +0.132, t-test p = .005).
This table shows molecular features associated with PDE2A-AS1 in patient tissues and cancer cell lines. In patient samples, PDE2A-AS1 shows the broadest associations at the RNA and protein expression levels, with TGCT recurring as the lineage with the largest associated feature set.
