Key result
Insufficient data provided to generate a clinical headline.
Why the study?
Aberrant de novo lipid synthesis and reprogrammed lipid metabolism are associated with pancreatic cancer development and progression, highlighting the need to review current knowledge for future individualized therapies.
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Effect estimate: null (95% CI null)
p-value: p=null
This review summarizes current knowledge on lipid metabolism and lipid droplets in pancreatic cancer and tumor stroma, highlighting potential targets for individualized therapies.
Should not yet change pancreatic cancer practice; leaves open lipid metabolism and droplets in tumor stroma for individualized therapeutic targeting.
Pancreatic ductal adenocarcinoma (PDAC) is projected to become the second deadliest cancer by 2030, and the overall 5-year survival rate is currently less than 7%. Cancer cells frequently exhibit reprogramming of their metabolic activity. It is increasingly recognized that aberrant de novo lipid synthesis and reprogrammed lipid metabolism are both associated with the development and progression of various cancers, including pancreatic cancer. In this review, the current knowledge about lipid metabolism and lipid droplets in pancreatic cancer is discussed. In the first part, molecular mechanisms of lipid metabolism and roles of enzymes involved in lipid metabolism which are relevant for pancreatic cancer research are presented. Further, preclinical studies and clinical trials with drugs/inhibitors targeting cancer metabolic systems in cancer are summarized. An increase of our knowledge in lipid metabolism in pancreatic cancer cells and in tumor stroma is important for developing novel strategies of future individualized therapies of pancreatic cancer.
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Sunami et al. (2018) conducted a null in pancreatic cancer. null vs. null was evaluated on null (null, 95% CI null, p=null). null.
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