Dual rectification of metabolism abnormality in pancreatic cancer by a programmed nanomedicine

Pancreatic ductal adenocarcinoma (PDAC) is a highly aggressive and lethal malignancy characterized by dysregulated energy and stromal metabolism. It is strongly supported by activated pancreatic stellate cells (PSC) which drive excessive desmoplasia and tumor growth via metabolic crosstalk. Herein, a programmed nanosystem is designed to dual rectify the metabolism abnormalities of the PDAC cells, which overexpress glucose transporter 1(GLUT1) and CD71, and the PSC for oncotherapy. The nanosystem is based on a tumor microenvironment-responsive liposome encapsulating an NF-κB inhibitor (TPCA-1) and a CD71 aptamer-linked Glut1 siRNA. TPCA-1 reverses the activated PSC to quiescence, which hampers metabolic support of the PSC to PDAC cells and bolsters the PDAC cell-targeting delivery of the siRNA. Aerobic glycolysis and the following enhancement of oxidative phosphorylation are restrained by the nano-modulation so as to amplify anti-PDAC efficacy in an orthotopic xenograft mouse model, which implies more personalized PDAC treatment based on different energy metabolic profiles. The activation of pancreatic stellate cells (PSCs) was found to promote the progression of Pancreatic ductal adenocarcinoma (PDAC) via metabolic crosstalk. Here, this group designs a liposome nanosystem encapsulating NF-κB inhibitor (TPCA-1) and CD71 aptamerlinked glucose transporter 1 (GLUT1) siRNA to dual rectify the metabolism abnormalities of PDAC cells and reverses the activated PSC to quiescence.