Literature DB >> 3120698

Analysis of tricarboxylic acid-cycle metabolism of hepatoma cells by comparison of 14CO2 ratios.

J K Kelleher1, B M Bryan, R T Mallet, A L Holleran, A N Murphy, G Fiskum.   

Abstract

The CO2-ratios method is applied to the analysis of abnormalities of TCA (tricarboxylic acid)-cycle metabolism in AS-30D rat ascites-hepatoma cells. This method utilizes steady-state 14CO2-production rates from pairs of tracers of the same compound to evaluate TCA-cycle flux patterns. Equations are presented that quantitatively convert CO2 ratios into estimates of probability of flux through TCA-cycle-related pathways. Results of this study indicated that the ratio of 14CO2 produced from [1,4-14C]succinate to 14CO2 produced from [2,3-14C]succinate was increased by the addition of glutamine (5 mM) to the medium. An increase in the succinate CO2 ratio is quantitatively related to an increased flux of unlabelled carbon into the TCA-cycle-intermediate pools. Analysis of 14C distribution in [14C]citrate derived from [2,3-14C]succinate indicated that flux from the TCA cycle to the acetyl-CoA-derived carbons of citrate was insignificant. Thus the increased succinate CO2 ratio observed in the presence of glutamine could only result from an increased flux of carbon into the span of the TCA cycle from citrate to oxaloacetate. This result is consistent with increased flux of glutamine to alpha-oxoglutarate in the incubation medium containing exogenous glutamine. Comparison of the pyruvate CO2 ratio, steady-state 14CO2 production from [2-14C]pyruvate versus [3-14C]pyruvate, with the succinate 14CO2 ratio detected flux of pyruvate to C4 TCA-cycle intermediates in the medium containing glutamine. This result was consistent with the observation that [14C]aspartate derived from [2-14C]pyruvate was labelled in C-2 and C-3. 14C analysis also produced evidence for flux of TCA-cycle carbon to alanine. This study demonstrates that the CO2-ratios method is applicable in the analysis of the metabolic properties of AS-30D cells. This methodology has verified that the atypical TCA-cycle metabolism previously described for AS-30D-cell mitochondria occurs in intact AS-30D rat hepatoma cells.

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Year:  1987        PMID: 3120698      PMCID: PMC1148327          DOI: 10.1042/bj2460633

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  21 in total

1.  Conversion of fatty acids to carbohydrate; application of isotopes to this problem and role of the Krebs cycle as a synthetic pathway.

Authors:  E O WEINMAN; E H STRISOWER; I L CHAIKOFF
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2.  Identification and properties of the nicotinamide adenine dinucleotide (phosphate)+-dependent malic enzyme in mouse ascites tumor mitochondria.

Authors:  L A Sauer; R T Dauchy
Journal:  Cancer Res       Date:  1978-06       Impact factor: 12.701

3.  A method for obtaining the 14C-isotope distribution in malate(C-2,3).

Authors:  S S Kent; C A Rinehart; W R Andersen
Journal:  Anal Biochem       Date:  1977-05-15       Impact factor: 3.365

4.  Establishment of a transplantable ascites variant of a rat hepatoma induced by 3'-methyl-4-dimethylaminoazobenzene.

Authors:  D F Smith; E F Walborg; J P Chang
Journal:  Cancer Res       Date:  1970-09       Impact factor: 12.701

5.  Complete stereochemical distribution of 14 C-isotope in citrate.

Authors:  S S Kent
Journal:  Anal Biochem       Date:  1972-10       Impact factor: 3.365

Review 6.  Membrane cholesterol, tumorigenesis, and the biochemical phenotype of neoplasia.

Authors:  P S Coleman; B B Lavietes
Journal:  CRC Crit Rev Biochem       Date:  1981

7.  Active oxidative decarboxylation of malate by mitochondria isolated from L-1210 ascites tumor cells.

Authors:  R G Hansford; A L Lehninger
Journal:  Biochem Biophys Res Commun       Date:  1973-03-17       Impact factor: 3.575

8.  Mitochondrial malic enzymes. Mitochondrial NAD(P)+-dependent malic enzyme activity and malate-dependent pyruvate formation are progression-linked in Morris hepatomas.

Authors:  L A Sauer; R T Dauchy; W O Nagel; H P Morris
Journal:  J Biol Chem       Date:  1980-05-10       Impact factor: 5.157

9.  Mitochondrial malic enzymes. An association between NAD(P)+-dependent malic enzyme and cell renewal in Sprague-Dawley rat tissues.

Authors:  W O Nagel; R T Dauchy; L A Sauer
Journal:  J Biol Chem       Date:  1980-05-10       Impact factor: 5.157

10.  Amino acids and glucose utilization by different metabolic pathways in ascites-tumour cells.

Authors:  P A Lazo
Journal:  Eur J Biochem       Date:  1981-06
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  7 in total

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Authors:  Z Kovacević; D Jerance; O Brkljac
Journal:  Biochem J       Date:  1988-06-01       Impact factor: 3.857

2.  Glutamine metabolism in AS-30D hepatoma cells. Evidence for its conversion into lipids via reductive carboxylation.

Authors:  A L Holleran; D A Briscoe; G Fiskum; J K Kelleher
Journal:  Mol Cell Biochem       Date:  1995-11-22       Impact factor: 3.396

3.  Acetoacetate metabolism in AS-30D hepatoma cells.

Authors:  D A Briscoe; G Fiskum; A L Holleran; J K Kelleher
Journal:  Mol Cell Biochem       Date:  1994-07-27       Impact factor: 3.396

4.  Maximum activities of key enzymes of glycolysis, glutaminolysis, pentose phosphate pathway and tricarboxylic acid cycle in normal, neoplastic and suppressed cells.

Authors:  M Board; S Humm; E A Newsholme
Journal:  Biochem J       Date:  1990-01-15       Impact factor: 3.857

5.  Control and function of the transamination pathways of glutamine oxidation in tumour cells.

Authors:  Z Kovacević; O Brkljac; K Bajin
Journal:  Biochem J       Date:  1991-01-15       Impact factor: 3.857

6.  Metabolic fate of the increased yeast amino Acid uptake subsequent to catabolite derepression.

Authors:  John S Hothersall; Aamir Ahmed
Journal:  J Amino Acids       Date:  2013-02-04

Review 7.  The clinical relevance of the metabolism of prostate cancer; zinc and tumor suppression: connecting the dots.

Authors:  Leslie C Costello; Renty B Franklin
Journal:  Mol Cancer       Date:  2006-05-15       Impact factor: 27.401

  7 in total

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