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        <datestamp>2026-09-25T05:31:19Z</datestamp>
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          <dc:title>Data Sheet 1_A palmitoylation-associated three-gene signature predicts prognosis, immune features, and drug sensitivity in gastric cancer: functional validation of CTHRC1.zip</dc:title>
          <dc:creator>Hongmei Sheng (6801131)</dc:creator>
          <dc:creator>Xuejun Li (133209)</dc:creator>
          <dc:creator>Chen Zhang (66790)</dc:creator>
          <dc:creator>Miaomiao Song (10755624)</dc:creator>
          <dc:creator>Juan Xu (225010)</dc:creator>
          <dc:creator>Jun Ma (9393)</dc:creator>
          <dc:subject>Genetic Immunology</dc:subject>
          <dc:subject>drug sensitivity</dc:subject>
          <dc:subject>gastric cancer</dc:subject>
          <dc:subject>palmitoylation-associated genes</dc:subject>
          <dc:subject>prognosis</dc:subject>
          <dc:subject>tumor microenvironment</dc:subject>
          <dc:description>Background&lt;p&gt;Gastric cancer (GC) is a heterogeneous malignancy that requires improved molecular tools for prognostic stratification. Protein palmitoylation regulates membrane localization and signaling, but the clinical relevance of palmitoylation-related genes (PRGs) in GC remains unclear.&lt;/p&gt;Methods&lt;p&gt;Gene Expression Omnibus, The Cancer Genome Atlas, and GeneCards data were integrated to identify PRGs. Differential expression analysis, weighted gene co-expression network analysis, and three machine-learning algorithms were used to select key genes. Diagnostic and prognostic performance was evaluated in TCGA-STAD, platform-specific GEO cohorts, and an institutional cohort of 80 paired tissues. Immune infiltration, single-cell RNA sequencing, immunotherapy-related indices, and GDSC-based drug sensitivity were analyzed. CTHRC1 was further examined using clinical specimens, cell assays, and xenografts.&lt;/p&gt;Results&lt;p&gt;Thirteen differentially expressed PRGs were identified, and SERPINE1, CTHRC1, and EGR1 were selected. The integrated diagnostic model achieved AUCs of 0.935 in TCGA-STAD, 1.000 in GSE54129, and 0.916 in GSE118916, respectively. The three-gene score stratified overall survival in the total, training, and testing TCGA-STAD cohorts and in GSE84437, GSE236522, and the institutional cohort. It remained independently associated with survival in multivariable analysis. High-risk tumors showed increased stromal and immune scores, altered immune-cell composition, higher checkpoint expression, and higher TIDE scores. Single-cell analysis localized SERPINE1 and CTHRC1 mainly to fibroblast-related compartments. CTHRC1 knockdown reduced GC-cell proliferation, clonogenicity, migration, invasion, and xenograft growth while increasing apoptosis.&lt;/p&gt;Conclusion&lt;p&gt;The SERPINE1/CTHRC1/EGR1 signature provides prognostic and immune-stromal information in GC, and the experiments support a tumor-promoting role for CTHRC1. The findings define a palmitoylation-associated transcriptional framework but do not establish a palmitoylation-dependent mechanism.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-25T05:31:19Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.3389/fimmu.2026.1893438.s001</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/Data_Sheet_1_A_palmitoylation-associated_three-gene_signature_predicts_prognosis_immune_features_and_drug_sensitivity_in_gastric_cancer_functional_validation_of_CTHRC1_zip/33993001</dc:relation>
          <dc:rights>CC BY 4.0</dc:rights>
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