Q-omics provides the consensus-scored NPPA-AS1 profile across patient tissues and cancer cell-line models. NPPA-AS1 expression is associated with patient survival in 27 of 34 cancer types, with the highest sampling consensus in ACC. Among the 18 cancer types available for tumor–normal comparison, NPPA-AS1 is differentially expressed in 10, with the highest sampling consensus in KICH. Additionally, NPPA-AS1 RNA expression shows 14,781 significant gene co-expression associations, with the highest sampling consensus in UVM. Together, these results highlight ACC, KICH, and UVM as cancer lineages where NPPA-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 NPPA-AS1 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes NPPA-AS1 survival associations across molecular data types. NPPA-AS1 RNA expression shows survival associations in the most cancer types (27). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible NPPA-AS1 RNA expression–survival associations across cancer types. High NPPA-AS1 expression shows unfavorable associations in ACC, LIHC, SKCM, LUSC and MESO, but favorable associations in READ. The ACC 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 ACC as the clearest survival context for NPPA-AS1 RNA expression.
This table summarizes NPPA-AS1 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 10. The strongest signals are observed in KICH for RNA.
This table ranks reproducible tumor–normal expression differences for NPPA-AS1. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. NPPA-AS1 shows lower tumor expression in KICH, BRCA and LUSC and higher tumor expression in LIHC, KIRC and STAD. The KICH box plot shows higher NPPA-AS1 RNA expression in normal versus tumor tissue (log2 FC = −0.402, t-test p < 0.001).
This table shows molecular features associated with NPPA-AS1 in patient tissues and cancer cell lines. In patient samples, NPPA-AS1 shows the broadest associations at the RNA and protein expression levels, with UVM recurring as the lineage with the largest associated feature set. In cancer cell lines, NPPA-AS1 RNA and mutation anchors are most strongly linked to RNA-expression features, especially in BLOOD_Leukemia, while CRISPR and shRNA rows add functional-dependency signals in BREAST.
