Q-omics provides the consensus-scored LINC02702 profile across patient tissues and cancer cell-line models. LINC02702 expression is associated with patient survival in 13 of 34 cancer types, with the highest sampling consensus in UVM. Among the 18 cancer types available for tumor–normal comparison, LINC02702 is differentially expressed in 6, with the highest sampling consensus in HNSC. Additionally, LINC02702 RNA expression shows 6,510 significant pathway-activity associations, with the highest sampling consensus in STAD. Together, these results highlight UVM, HNSC, and STAD as cancer lineages where LINC02702 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 LINC02702 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes LINC02702 survival associations across molecular data types. LINC02702 RNA expression shows survival associations in the most cancer types (13). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible LINC02702 RNA expression–survival associations across cancer types. High LINC02702 expression shows unfavorable associations in UVM, PCPG and COAD, but favorable associations in UCS, MESO and KIRC. The UVM 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 UVM as the clearest survival context for LINC02702 RNA expression.
This table summarizes LINC02702 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 HNSC for RNA.
This table ranks reproducible tumor–normal expression differences for LINC02702. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. LINC02702 shows lower tumor expression in CHOL and higher tumor expression in HNSC, BRCA, UCEC, LUSC and LIHC. The HNSC box plot shows higher LINC02702 RNA expression in tumor versus normal tissue (log2 FC = +0.034, t-test p = .017).
This table shows molecular features associated with LINC02702 in patient tissues and cancer cell lines. In patient samples, LINC02702 shows the broadest associations at the RNA and protein expression levels, with STAD recurring as the lineage with the largest associated feature set.
