Published online Dec 16, 2021. doi: 10.12998/wjcc.v9.i35.10884
Peer-review started: June 25, 2021
First decision: August 19, 2021
Revised: September 1, 2021
Accepted: October 27, 2021
Article in press: October 27, 2021
Published online: December 16, 2021
Processing time: 167 Days and 16.5 Hours
Finding specific prognostic markers is important for pancreatic cancer. Understanding the relationship between lipid metabolism-related genes and pancreatic cancer is helpful to improve its prognosis.
To construct a novel model to predict the prognosis of pancreatic cancer.
To investigate the characteristics of lipid metabolites in pancreatic cancer and construct a prognostic polygene signature of differentially expressed genes related to lipid metabolism.
Lipid metabolomics analysis was conducted to explore differences in lipid metabolites between pancreatic cancer tissues and paracancerous tissues. A predictive model of lipid metabolism genes associated with pancreatic cancer was established using a cohort from The Cancer Genome Atlas.
Lipid metabolomics analysis showed that the lipid metabolites phosphatidylcholine, phosphatidyl ethanolamine, phosphatidylethanol, phosphatidylmethanol, phosphatidylserines and diacylglyceryl trimethylhomoserine were significantly higher in cancer tissues. A 4-gene signature model, including GALNT16, FADS3, CERS4 and ABO, was developed to predict the prognosis of pancreatic cancer.
Differentially expressed genes related to lipid metabolism reflected abnormal lipid metabolism in pancreatic cancer. A novel predictive model of a 4-lipid metabolism-related gene signature contributed to the prediction of pancreatic cancer prognosis.
New gene markers and models are needed to predict prognosis because of the high heterogeneity of pancreatic cancer.
