| Literature DB >> 28963851 |
Kumar Pichumani1,2, Tomoyuki Mashimo3,4, Vamsidhara Vemireddy4,5, Omkar B Ijare1, Bruce E Mickey6, Craig R Malloy5,7,8,9, Isaac Marin-Valencia10, David S Baskin1,2, Robert M Bachoo3,4,5,11, Elizabeth A Maher3,4,5,11.
Abstract
Malignant brain tumors are known to utilize acetate as an alternate carbon source in the citric acid cycle for their bioenergetics. 13 C NMR-based isotopomer analysis has been used to measure turnover of 13 C-acetate carbons into glutamate and glutamine pools in tumors. Plasma from the patients infused with [1,2-13 C]acetate further revealed the presence of 13 C isotopomers of glutamine, glucose, and lactate in the circulation that were generated due to metabolism of [1,2-13 C]acetate by peripheral organs. In the tumor cells, [4-13 C] and [3,4-13 C]glutamate and glutamine isotopomers were generated from blood-borne 13 C-labeled glucose and lactate which were formed due to [1,2-13 C[acetate metabolism of peripheral tissues. [4,5-13 C] and [3,4,5-13 C]glutamate and glutamine isotopomers were produced from [1,2-13 C]acetyl-CoA that was derived from direct oxidation of [1,2-13 C] acetate in the tumor. Major portion of C4 13 C fractional enrichment of glutamate (93.3 ± 0.02%) and glutamine (90.9 ± 0.03%) were derived from [1,2-13 C]acetate-derived acetyl-CoA.Entities:
Keywords: 13C isotopomer; [1,2-13C]acetate; acetyl-CoA; glutamate and glutamine synthesis; peripheral metabolism
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Year: 2017 PMID: 28963851 PMCID: PMC5763554 DOI: 10.1002/1873-3468.12867
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124