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Pancreatic ductal adenocarcinoma (PDAC) is a lethal malignancy and is refractory to available treatments. Delineating the regulatory mechanisms of metabolic reprogramming, a key event in pancreatic cancer progression, may identify candidate targets with potential therapeutic significance. We hypothesized that inflammatory signaling pathways regulate metabolic adaptations in pancreatic cancer. Metabolic profiling of tumors from PDAC patients with a high- (>median, n = 31) and low-NOS2 (inducible nitric oxide synthase;

More information Original publication

DOI

10.1002/ijc.32733

Type

Journal article

Publication Date

2020-06-01T00:00:00+00:00

Volume

146

Pages

3160 - 3169

Total pages

9

Keywords

RUNX3, kynurenine, nitric oxide, pancreatic cancer, prognosis, therapeutic targets, Carcinoma, Pancreatic Ductal, Cell Movement, Core Binding Factor Alpha 3 Subunit, Humans, Indoleamine-Pyrrole 2,3,-Dioxygenase, Kynurenine, Neoplasm Invasiveness, Nitric Oxide, Nitric Oxide Synthase Type II, Pancreatic Neoplasms, Receptors, Aryl Hydrocarbon, Signal Transduction, Spheroids, Cellular, Tryptophan, Tumor Cells, Cultured