Q-omics provides the consensus-scored SDF4 profile across patient tissues and cancer cell-line models. SDF4 expression is associated with patient survival in 20 of 34 cancer types, with the highest sampling consensus in ACC. Among the 18 cancer types available for tumor–normal comparison, SDF4 is differentially expressed in 13, with the highest sampling consensus in HNSC. Additionally, SDF4 RNA expression shows 19,966 significant gene co-expression associations, with the highest sampling consensus in ACC. Together, these results highlight ACC, and HNSC as cancer lineages where SDF4 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 SDF4 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes SDF4 survival associations across molecular data types. SDF4 RNA expression shows survival associations in the most cancer types (20), followed by mutation status (6) and mass-spec protein abundance (5). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible SDF4 RNA expression–survival associations across cancer types. High SDF4 expression shows unfavorable associations in ACC, KICH, CESC, LGG and LIHC, but favorable associations in SCLC. 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 SDF4 RNA expression.
This table summarizes SDF4 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 13, while mass-spec protein shows differences in 5. The strongest signals are observed in KIRC for RNA and LUAD for protein.
This table ranks reproducible tumor–normal expression differences for SDF4. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. SDF4 shows lower tumor expression in KICH and higher tumor expression in HNSC, KIRC, STAD, LIHC and LUAD. The HNSC box plot shows higher SDF4 RNA expression in tumor versus normal tissue (log2 FC = +1.005, t-test p < 0.001).
This table shows molecular features associated with SDF4 in patient tissues and cancer cell lines. In patient samples, SDF4 shows the broadest associations at the RNA and protein expression levels, with ACC recurring as the lineage with the largest associated feature set. In cancer cell lines, SDF4 RNA and mutation anchors are most strongly linked to RNA-expression features, especially in OVARY, while CRISPR and shRNA rows add functional-dependency signals in SOFT_TISSUE and BLOOD_Lymphoma.
