NMR Spectroscopic Investigation of the Effect of LDH inhibitor Sodium oxamate on Glucose metabolism in cancer cell
ORAL
Abstract
Sodium oxamate is an inhibitor of lactate dehydrogenase (LDH) that specifically inhibit LDH-A,
an important enzyme that is active in most of tissues catalyzes the reversible conversion of pyruvate to lactate.
In this work, we have investigated via carbon-13 nuclear magnetic resonance the concentration dependence of sodium oxamate and the role of glutamine on [1-13C] glucose metabolism in a variety of cultured cancers cell including renal cell carcinoma (786-O), hepatocellular carcinoma (HepG-2), and glioblastoma (SfXL cells). Our results reveal that highest concentration of sodium oxamate affect lactate production and other glucose metabolites in these cancer cell. Intra- and extra-cellular metabolic products of glucose will be discussed in light of the key role of glutamine in glucose metabolism. . This study is supported by the Welch Foundation grant AT-1877-20180324, DOD grants W18XWH-17-1-0303 and W81XWH-19-1-0741, Cancer Prevention and Research Institute of Texas (CPRIT) grant RP180716, and the UTD Collaborative Biomedical Research Award (CoBRA)
an important enzyme that is active in most of tissues catalyzes the reversible conversion of pyruvate to lactate.
In this work, we have investigated via carbon-13 nuclear magnetic resonance the concentration dependence of sodium oxamate and the role of glutamine on [1-13C] glucose metabolism in a variety of cultured cancers cell including renal cell carcinoma (786-O), hepatocellular carcinoma (HepG-2), and glioblastoma (SfXL cells). Our results reveal that highest concentration of sodium oxamate affect lactate production and other glucose metabolites in these cancer cell. Intra- and extra-cellular metabolic products of glucose will be discussed in light of the key role of glutamine in glucose metabolism. . This study is supported by the Welch Foundation grant AT-1877-20180324, DOD grants W18XWH-17-1-0303 and W81XWH-19-1-0741, Cancer Prevention and Research Institute of Texas (CPRIT) grant RP180716, and the UTD Collaborative Biomedical Research Award (CoBRA)
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Presenters
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Asiye Asaadzade
University of Texas at Dallas
Authors
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Asiye Asaadzade
University of Texas at Dallas
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Lloyd Lumata
University of Texas at Dallas