Increased glucose availability sensitizes pancreatic cancer to chemotherapy

Author:

Vaziri-Gohar AliORCID,Hue Jonathan J.,Abbas AtaORCID,Graor Hallie J.,Hajihassani Omid,Zarei MehrdadORCID,Titomihelakis George,Feczko John,Rathore Moeez,Chelstowska Sylwia,Loftus Alexander W.,Wang Rui,Zarei Mahsa,Goudarzi MaryamORCID,Zhang Renliang,Willard Belinda,Zhang Li,Kresak Adam,Willis Joseph E.,Wang Gi-Ming,Tatsuoka Curtis,Salvino Joseph M.ORCID,Bederman Ilya,Brunengraber Henri,Lyssiotis Costas A.,Brody Jonathan R.,Winter Jordan M.ORCID

Abstract

AbstractPancreatic Ductal Adenocarcinoma (PDAC) is highly resistant to chemotherapy. Effective alternative therapies have yet to emerge, as chemotherapy remains the best available systemic treatment. However, the discovery of safe and available adjuncts to enhance chemotherapeutic efficacy can still improve survival outcomes. We show that a hyperglycemic state substantially enhances the efficacy of conventional single- and multi-agent chemotherapy regimens against PDAC. Molecular analyses of tumors exposed to high glucose levels reveal that the expression of GCLC (glutamate-cysteine ligase catalytic subunit), a key component of glutathione biosynthesis, is diminished, which in turn augments oxidative anti-tumor damage by chemotherapy. Inhibition of GCLC phenocopies the suppressive effect of forced hyperglycemia in mouse models of PDAC, while rescuing this pathway mitigates anti-tumor effects observed with chemotherapy and high glucose.

Funder

University Hospitals research start-up package

Loyola University Chicago research start-up package

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry,Multidisciplinary

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