The value of lipid metabolism-related genes in pancreatic cancer immunotherapy and drug prediction.
1/5 보강
[BACKGROUND] Pancreatic cancer represents a significant global health burden.
APA
Xue R, Tao Z, et al. (2025). The value of lipid metabolism-related genes in pancreatic cancer immunotherapy and drug prediction.. Journal of gastrointestinal oncology, 16(6), 2827-2846. https://doi.org/10.21037/jgo-2025-507
MLA
Xue R, et al.. "The value of lipid metabolism-related genes in pancreatic cancer immunotherapy and drug prediction.." Journal of gastrointestinal oncology, vol. 16, no. 6, 2025, pp. 2827-2846.
PMID
41522758 ↗
Abstract 한글 요약
[BACKGROUND] Pancreatic cancer represents a significant global health burden. Although dysregulated lipid metabolism and its associated inflammation drive tumorigenesis, their molecular interplay remains incompletely understood. This bioinformatics study investigates lipid metabolism-related genes (LMRGs) for prognostic prediction and treatment guidance in pancreatic cancer.
[METHODS] LMRGs were obtained from the Gene Set Enrichment Analysis (GSEA) database, while messenger ribonucleic acid (mRNA) expression profiles and clinical information were downloaded from The Cancer Genome Atlas (TCGA), Genotype-Tissue Expression (GTEx), and International Cancer Genome Consortium (ICGC) databases. Cox regression analysis and the least absolute shrinkage and selection operator (LASSO) regression analysis were employed to screen prognosis-related genes, followed by the construction of a risk prediction model. Patients were stratified into high- and low-risk groups for prognosis and immune infiltration comparison. Potential therapeutic drugs for pancreatic cancer were predicted using the DSigDB database based on the identified LMRGs.
[RESULTS] We successfully established and validated a prognostic prediction model for pancreatic cancer patients based on six LMRGs (, , , , , and ). The 1-, 3-, and 5-year area under the receiver operating characteristic (ROC) curve values were 0.623, 0.698, and 0.720, respectively. Immune infiltration analysis showed that after prognostic risk stratification using the six-gene signature, the high-risk group had higher proportions of M0 macrophages and neutrophils. Furthermore, the expression of eight immune checkpoint-related genes was significantly increased in the high-risk group. DSigDB database analysis revealed four possible therapeutic drugs for pancreatic cancer: prolinedithiocarbamate, isoliquiritigenin, aspirin, and resveratrol.
[CONCLUSIONS] The risk score based on the six LMRGs provides prognostic insights for pancreatic cancer. High-risk pancreatic cancer populations are potentially associated with an immunosuppressive microenvironment. Candidate drugs screened based on LMRGs offer new possibilities for personalized treatment of pancreatic cancer.
[METHODS] LMRGs were obtained from the Gene Set Enrichment Analysis (GSEA) database, while messenger ribonucleic acid (mRNA) expression profiles and clinical information were downloaded from The Cancer Genome Atlas (TCGA), Genotype-Tissue Expression (GTEx), and International Cancer Genome Consortium (ICGC) databases. Cox regression analysis and the least absolute shrinkage and selection operator (LASSO) regression analysis were employed to screen prognosis-related genes, followed by the construction of a risk prediction model. Patients were stratified into high- and low-risk groups for prognosis and immune infiltration comparison. Potential therapeutic drugs for pancreatic cancer were predicted using the DSigDB database based on the identified LMRGs.
[RESULTS] We successfully established and validated a prognostic prediction model for pancreatic cancer patients based on six LMRGs (, , , , , and ). The 1-, 3-, and 5-year area under the receiver operating characteristic (ROC) curve values were 0.623, 0.698, and 0.720, respectively. Immune infiltration analysis showed that after prognostic risk stratification using the six-gene signature, the high-risk group had higher proportions of M0 macrophages and neutrophils. Furthermore, the expression of eight immune checkpoint-related genes was significantly increased in the high-risk group. DSigDB database analysis revealed four possible therapeutic drugs for pancreatic cancer: prolinedithiocarbamate, isoliquiritigenin, aspirin, and resveratrol.
[CONCLUSIONS] The risk score based on the six LMRGs provides prognostic insights for pancreatic cancer. High-risk pancreatic cancer populations are potentially associated with an immunosuppressive microenvironment. Candidate drugs screened based on LMRGs offer new possibilities for personalized treatment of pancreatic cancer.
🏷️ 키워드 / MeSH 📖 같은 키워드 OA만
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