ArticleDiscover oncology2026
Construction of an efferocytosis related signature to predict the prognosis of pancreatic ductal adenocarcinoma.
Article in Discover oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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6 authors.
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Abstract
backgroundPancreatic ductal adenocarcinoma (PDAC) is a highly lethal cancer with a poor prognosis. Efferocytosis can both promote and inhibit tumor progression, yet its role in PDAC remains largely unexplored.
methodsThe data were obtained from The Cancer Genome Atlas (TCGA) and the International Cancer Genome Consortium (ICGC) databases. GeneMANIA was employed to construct the protein-protein interaction network. This study explored the relationship between efferocytosis-related genes and PDAC prognosis using survival analysis, mutation spectrum assessment, evaluation of the immune microenvironment (ssGSEA), and prediction of treatment response (TIDE).
resultsEighteen efferocytosis-related genes were highly expressed in PDAC, and their mutations were associated with poorer patient survival. Notably, high expression of key genes such as AGER, STAB2, and ICAM3 was linked to better overall survival (OS) and progression-free survival (PFS), whereas elevated expression of AXL and HAVCR1 predicted a worse prognosis. Based on these findings, a prognostic signature (EFR-Signature) was developed that can independently predict patient outcomes. Patients classified as low-risk exhibited stronger antitumor immune activity and greater sensitivity to immunotherapy.
conclusionsHAVCR1, AGER, AXL, STAB2, and ICAM3 are closely associated with the prognosis of PDAC. A prognostic signature based on these genes can serve as an independent predictor of patient outcomes.
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