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Reductive carboxylation supports growth in tumour cells with defective mitochondria.
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PMID:  22101431     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Mitochondrial metabolism provides precursors to build macromolecules in growing cancer cells. In normally functioning tumour cell mitochondria, oxidative metabolism of glucose- and glutamine-derived carbon produces citrate and acetyl-coenzyme A for lipid synthesis, which is required for tumorigenesis. Yet some tumours harbour mutations in the citric acid cycle (CAC) or electron transport chain (ETC) that disable normal oxidative mitochondrial function, and it is unknown how cells from such tumours generate precursors for macromolecular synthesis. Here we show that tumour cells with defective mitochondria use glutamine-dependent reductive carboxylation rather than oxidative metabolism as the major pathway of citrate formation. This pathway uses mitochondrial and cytosolic isoforms of NADP(+)/NADPH-dependent isocitrate dehydrogenase, and subsequent metabolism of glutamine-derived citrate provides both the acetyl-coenzyme A for lipid synthesis and the four-carbon intermediates needed to produce the remaining CAC metabolites and related macromolecular precursors. This reductive, glutamine-dependent pathway is the dominant mode of metabolism in rapidly growing malignant cells containing mutations in complex I or complex III of the ETC, in patient-derived renal carcinoma cells with mutations in fumarate hydratase, and in cells with normal mitochondria subjected to acute pharmacological ETC inhibition. Our findings reveal the novel induction of a versatile glutamine-dependent pathway that reverses many of the reactions of the canonical CAC, supports tumour cell growth, and explains how cells generate pools of CAC intermediates in the face of impaired mitochondrial metabolism.
Authors:
Andrew R Mullen; William W Wheaton; Eunsook S Jin; Pei-Hsuan Chen; Lucas B Sullivan; Tzuling Cheng; Youfeng Yang; W Marston Linehan; Navdeep S Chandel; Ralph J DeBerardinis
Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural; Research Support, N.I.H., Intramural; Research Support, Non-U.S. Gov't     Date:  2011-11-20
Journal Detail:
Title:  Nature     Volume:  481     ISSN:  1476-4687     ISO Abbreviation:  Nature     Publication Date:  2012 Jan 
Date Detail:
Created Date:  2012-01-19     Completed Date:  2012-03-06     Revised Date:  2013-06-27    
Medline Journal Info:
Nlm Unique ID:  0410462     Medline TA:  Nature     Country:  England    
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Languages:  eng     Pagination:  385-8     Citation Subset:  IM    
Affiliation:
Department of Pediatrics, University of Texas - Southwestern Medical Center at Dallas, Dallas, Texas 75390-9063, USA.
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MeSH Terms
Descriptor/Qualifier:
Acetyl Coenzyme A / metabolism
Animals
Carcinoma, Renal Cell / genetics,  metabolism,  pathology
Cell Hypoxia
Cell Line, Tumor
Citric Acid / metabolism
Electron Transport
Electron Transport Complex I / metabolism
Electron Transport Complex III / metabolism
Fumarate Hydratase / genetics,  metabolism
Glucose / metabolism
Glutamine / metabolism
Humans
Isocitrate Dehydrogenase / metabolism
Kidney Neoplasms / genetics,  metabolism,  pathology
Mice
Mitochondria / metabolism*,  pathology*
NADP / metabolism
Neoplasms / metabolism*,  pathology*
Grant Support
ID/Acronym/Agency:
5T32GM083831/GM/NIGMS NIH HHS; DK078933/DK/NIDDK NIH HHS; K01 DK078933-03/DK/NIDDK NIH HHS; K08 DK072565-06/DK/NIDDK NIH HHS; K08DK072565/DK/NIDDK NIH HHS; P41 RR002584-22/RR/NCRR NIH HHS; P41 RR002584-23/RR/NCRR NIH HHS; R01 CA123067-05/CA/NCI NIH HHS; R01 CA157996-01/CA/NCI NIH HHS; R01CA123067/CA/NCI NIH HHS; R01CA157996/CA/NCI NIH HHS; RR02584/RR/NCRR NIH HHS; T32 CA009560-20/CA/NCI NIH HHS; T32 GM008061-30/GM/NIGMS NIH HHS; T32 GM083831/GM/NIGMS NIH HHS; T32 GM083831-04/GM/NIGMS NIH HHS; T32CA009560/CA/NCI NIH HHS; T32GM008061/GM/NIGMS NIH HHS
Chemical
Reg. No./Substance:
50-99-7/Glucose; 53-59-8/NADP; 56-85-9/Glutamine; 72-89-9/Acetyl Coenzyme A; 77-92-9/Citric Acid; EC 1.1.1.41/Isocitrate Dehydrogenase; EC 1.1.1.41/isocitrate dehydrogenase 2, human; EC 1.1.1.42./IDH1 protein, human; EC 1.10.2.2/Electron Transport Complex III; EC 1.6.5.3/Electron Transport Complex I; EC 4.2.1.2/Fumarate Hydratase
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Journal Information
Journal ID (nlm-journal-id): 0410462
Journal ID (pubmed-jr-id): 6011
Journal ID (nlm-ta): Nature
ISSN: 0028-0836
ISSN: 1476-4687
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nihms-submitted publication date: Day: 17 Month: 10 Year: 2011
Electronic publication date: Day: 20 Month: 11 Year: 2011
pmc-release publication date: Day: 19 Month: 7 Year: 2012
Volume: 481 Issue: 7381
First Page: 385 Last Page: 388
ID: 3262117
PubMed Id: 22101431
DOI: 10.1038/nature10642
ID: nihpa331574

Reductive carboxylation supports growth in tumor cells with defective mitochondria
Andrew R. Mullen1
William W. Wheaton78
Eunsook S. Jin23
Pei-Hsuan Chen1
Lucas B. Sullivan78
Tzuling Cheng1
Youfeng Yang6
W. Marston Linehan6
Navdeep S. Chandel78
Ralph J. DeBerardinis145
1Department of Pediatrics, University of Texas – Southwestern Medical Center at Dallas, Dallas, TX 75390-9063
2Department of Internal Medicine, University of Texas – Southwestern Medical Center at Dallas, Dallas, TX 75390-9063
3Advanced Imaging Research Center, University of Texas – Southwestern Medical Center at Dallas, Dallas, TX 75390-9063
4McDermott Center for Human Growth and Development, University of Texas – Southwestern Medical Center at Dallas, Dallas, TX 75390-9063
5Harold C. Simmons Comprehensive Cancer Center, University of Texas – Southwestern Medical Center at Dallas, Dallas, TX 75390-9063
6Urologic Oncology Branch, National Cancer Institute, Bethesda, MD 20892
7Department of Medicine, Northwestern University, Chicago, IL 60611-3008
8Department of Cell & Molecular Biology, Northwestern University, Chicago, IL 60611-3008
Correspondence: Correspondence and requests for materials should be addressed to ralph.deberardinis@utsouthwestern.edu or nav@northwestern.edu

Mitochondrial metabolism provides precursors to build macromolecules in growing cancer cells1,2. In normally-functioning tumor cell mitochondria, oxidative metabolism of glucose- and glutamine-derived carbon produces citrate and acetyl-CoA for lipid synthesis, which is required for tumorigenesis3. Yet some tumors harbor mutations in the citric acid cycle (CAC) or electron transport chain (ETC) that disable normal oxidative mitochondrial function47, and it is unknown how cells from such tumors generate precursors for macromolecular synthesis. Here we show that tumor cells with defective mitochondria use glutamine-dependent reductive carboxylation rather than oxidative metabolism as the major pathway of citrate formation. This pathway uses mitochondrial and cytosolic isoforms of NADP+/NADPH-dependent isocitrate dehydrogenase, and subsequent metabolism of glutamine-derived citrate provides both the acetyl-CoA for lipid synthesis and the 4-carbon intermediates needed to produce remaining CAC metabolites and related macromolecular precursors. This reductive, glutamine-dependent pathway is the dominant mode of metabolism in rapidly-growing malignant cells containing mutations in complex I or complex III of the ETC, in patient-derived renal carcinoma cells with mutations in fumarate hydratase (FH), and in cells with normal mitochondria subjected to acute pharmacological ETC inhibition. Our findings reveal the novel induction of a versatile glutamine-dependent pathway that reverses many of the reactions of the canonical CAC, supports tumor cell growth, and explains how cells generate pools of CAC intermediates in the face of impaired mitochondrial metabolism.

We first studied the metabolism of isogenic 143B human osteosarcoma cells that contained or lacked a loss-of-function mutation in ETC complex III (cytochrome b-c1 complex). These cell lines were generated by depleting 143B mitochondrial DNA (mtDNA) and repopulating with either wild-type mtDNA or mtDNA containing a frameshift mutation in the gene encoding cytochrome b (cytb), an essential complex III component8. Despite lack of respiration and complex III function in the mutants8, both wild-type (143Bwt) and cytb-mutant (143Bcytb) cells form colonies in soft agar9 and proliferate at comparable rates (Supplementary Fig. 1a), making these cells a good model to study growth during mitochondrial dysfunction. Both cell lines had detectable CAC intermediates, although citrate was less abundant and succinate was significantly more abundant in the 143Bcytb cells (Supplementary Fig. 1b). As expected for cells with defective oxidative phosphorylation, 143Bcytb cells had higher glucose consumption and lactate production than 143Bwt cells, indicating a metabolic shift towards aerobic glycolysis (Fig. 1a). To determine the effects of cytb mutation on the metabolic fates of glucose, we cultured both cell lines in medium containing D[U-13C]glucose and measured 13C enrichment of intracellular metabolites by mass spectrometry. In 143Bwt cells, most citrate molecules contained glucose-derived 13C (Fig. 1b). Citrate m+2 results from oxidative decarboxylation of glucose-derived pyruvate by pyruvate dehydrogenase (PDH) to form [1,2-13C]acetyl-coA, followed by condensation with an unlabeled oxaloacetate (OAA). Processing of citrate m+2 around one turn of the CAC produces citrate m+4 (Supplementary Fig. 2). In 143Bcytb cells, most citrate contained no glucose carbon (m+0), indicating suppressed PDH contribution to acetyl-CoA (Fig. 1b). Fumarate and malate m+2 were also decreased (Supplementary Fig. 1c,d).

Glutamine is a major respiratory substrate in cancer cells, providing energy and anaplerotic carbon for growth3,10. Both 143Bwt and 143Bcytb cells require glutamine for colony formation, implying a respiration-independent function for glutamine in cell growth9. 143Bcytb and 143Bwt cells consumed glutamine at similar rates (Fig. 1a). We cultured both cell lines with L[U-13C]glutamine to define the metabolic fates of glutamine. Similar to other glutamine-dependent cancer cells11, 143Bwt cells used glutamine as the major anaplerotic precursor, resulting in a large amount of fumarate, malate and citrate m+4 (Fig. 1c,d; Supplementary Figs. 1e and 3, top). In contrast, 143Bcytb cells produced only trace quantities of citrate m+4. Instead, they produced citrate m+5 through reductive carboxylation of glutamine-derived α-ketoglutarate (Fig. 1c). This reaction involves addition of an unlabeled carbon by isocitrate dehydrogenase (IDH) acting in reverse relative to the canonical oxidative CAC12. Cleavage of citrate m+5 by ATP-citrate lyase then produces acetyl-CoA m+2 and OAA m+3, with the unlabeled carbon retained on OAA (Supplementary Fig. 3, bottom). Examination of other CAC metabolites in 143Bcytb cells revealed that they were formed downstream of citrate m+5 and OAA m+3. These cells contained abundant malate and fumarate m+3, which was essentially absent from 143Bwt cells (Fig. 1d and Supplementary Fig. 1e). Thus these metabolites are generated from reductive, rather than oxidative glutamine metabolism (Fig. 1e). Succinate was formed through both reductive and oxidative glutamine metabolism in 143Bcytb cells (Supplementary Fig. 1f). Glutamine-dependent reductive carboxylation was also observed in 143Bcytb cells cultured in medium containing a full complement of amino acids (Supplementary Fig. 4), and in cells with a genetic defect in ETC complex I (Supplementary Fig. 5).

To determine which of the three IDH isoforms contributed to reductive carboxylation, we used RNA interference (RNAi) to silence expression of IDH1, IDH2 and IDH3 in 143Bcytb cells and measured glutamine-derived 13C labeling in citrate. Silencing either of the NADP+/NADPH-dependent IDH isoforms, IDH1 or IDH2, reduced citrate m+5 in cells cultured with L[U-13C]glutamine and silencing both at once further reduced citrate m+5 (Fig. 2a,b). Conversion of glutamine to glutamate was unaffected (Fig. 2b). Silencing IDH3, the mitochondrial NAD+/NADH-dependent isoform, had no effect on labeling (Fig. 2a,b). Thus reductive carboxylation in 143Bcytb cells involves IDH1 and IDH2, but not IDH3. Because IDH1 and IDH2 proteins are localized primarily in the cytoplasm and mitochondria, respectively, of both cell lines (Supplementary Fig. 6), the data suggest that reductive carboxylation in 143Bcytb cells may occur in either compartment.

To determine whether IDH1 and IDH2 are required for growth, we stably silenced each enzyme using lentiviral RNAi. In 143Bwt cells, silencing either isoform reduced cell growth (Supplementary Fig. 7), consistent with findings in other cancer cells with normal mitochondria13. In 143Bcytb cells, a similar growth reduction occurred when either isoform was silenced (Supplementary Fig. 7). Thus both IDH1 and IDH2 support growth in cells that use glutamine-dependent reductive carboxylation.

We next determined whether reductive glutamine metabolism contributed to lipogenesis, a biosynthetic activity required for cancer cell growth. Both 143Bwt and 143Bcytb cells produced fatty acids de novo, as indicated by incorporation of 3H2O into lipids (Fig. 3a). The two cell lines were then cultured with 14C-labeled lipogenic substrates to examine carbon preferences for lipogenesis (Fig. 3a). Both cell lines had an intact pathway of lipogenesis from exogenously-supplied acetate. The enhanced labeling in 143Bcytb cells likely resulted from an increased specific activity of the intracellular 2-carbon pool because of suppressed PDH. Lipids derived from 143Bcytb cells contained little radioactivity from glucose, but abundant radioactivity from glutamine, indicating a switch in the extent to which these nutrients supplied lipogenesis. To quantify the contribution of glucose and glutamine to lipogenic acetyl-CoA, cells were cultured in medium containing either D[U-13C]glucose and unlabeled glutamine, or L[U-13C]glutamine and unlabeled glucose. Extracted lipids were analyzed by 13C NMR. Because fatty acids are synthesized by the sequential addition of 2-carbon units, analyzing 13C-13C coupling between the ω-1 and ω-2 carbons – which enter the fatty acyl chain on different 2-carbon units – enables calculation of 13C enrichment in lipogenic acetyl-CoA3. In the ω-1 multiplet, 13C-13C coupling produces a triplet when two 13C-labeled 2-carbon units are added in succession, whereas one labeled and one unlabeled unit produce a doublet (Fig. 3b). Therefore 13C labeling in lipogenic acetyl-CoA is proportional to the contribution of the triplet to the overall area of the ω-1 multiplet. In 143Bwt cells cultured with D[U-13C]glucose, the ω-1 resonance was dominated by the triplet, which accounted for 65% of the total area (Fig. 3c, left). Glutamine was a minor source of fatty acyl carbon, as the triplet accounted for only 15% of the area when the cells were cultured with L[U-13C]glutamine (Fig. 3d, left). This pattern was reversed in the 143Bcytb cells, with glutamine providing 67% of the lipogenic carbon (Fig. 3c,d, right; Supplementary Fig. 8a). Thus, reductive glutamine metabolism was the major pathway of fatty acid production in newly-synthesized lipids during 143Bcytb growth.

Although most cancer cells have functional mitochondria, a subset of human tumors harbors mutations that impair mitochondrial metabolism. Two major classes of mutations occur in genes required for function of the CAC enzymes succinate dehydrogenase (SDHA-D, SDHAF2) or fumarate hydratase (FH)14. To test whether glutamine-dependent reductive carboxylation occurs in tumor cells harboring these mutations, we studied UOK262 cells derived from a renal tumor in a patient with hereditary leiomyomatosis renal cell carcinoma syndrome. In this syndrome, affected individuals inherit one loss-of-function FH allele and their tumors display loss of heterozygosity for the FH locus15. UOK262 cells are defective in respiration and devoid of FH activity15. They failed to survive culture in glucose-free medium containing galactose and glutamine (Fig. 4a), a condition that forces cells to use mitochondrial metabolism to generate ATP16. Lack of FH activity precludes the use of glutamine as a carbon source in the conventional oxidative CAC. Yet the UOK262 cells required glutamine to proliferate (Fig. 4b). Culture of these cells with D[U-13C]glucose produced mass isotopomer data similar to 143Bcytb cells, with minimal formation of citrate m+2 (Fig. 4c, left). In cells cultured with L[U-13C]glutamine, the most abundant mass isotopomer of citrate was m+5 formed by reductive carboxylation (Fig. 4c, left). Fumarate was predominantly formed through oxidative glutamine metabolism, producing fumarate m+4 (Fig. 4c, middle). However, a large fraction of the malate pool (m+3) was formed via citrate cleavage and subsequent reductive metabolism (Fig. 4c, right). Lipid labeling using D[U-13C]glucose or L[U-13C]glutamine revealed that, like 143Bcytb cells, glutamine is the major carbon source for fatty acid synthesis (Supplementary Fig. 8b). Thus these cancer cells produce CAC intermediates using two distinct pathways to compensate for the loss of FH enzyme activity: oxidative metabolism of glutamine to fumarate, and glutamine-dependent reductive carboxylation to produce citrate, acetyl-CoA for lipogenesis, and remaining 4-carbon CAC intermediates.

Finally, we tested whether glutamine-dependent reductive carboxylation was unique to cells with permanent abnormalities in mitochondrial metabolism. 143Bwt cells and transformed mouse embryonic fibroblasts (MEFs) were subjected to acute ETC inhibition. Exposure to inhibitors of complex III (antimycin) or complex I (rotenone) induced a switch from oxidative to reductive metabolism of glutamine (Fig. 4d, Supplementary Fig. 9a). Enhanced reductive carboxylation was evident one hour after ETC inhibition and was not eliminated by pre-treatment with the protein synthesis inhibitor cycloheximide (Supplementary Fig. 9b,c). Metformin, an antidiabetic agent that inhibits respiration through effects on complex I17, also induced glutamine-dependent reductive carboxylation at high doses (Fig. 4d, Supplementary Fig. 9a). Interestingly, doses that mimicked plasma concentrations in patients with acute metformin toxicity and lactic acidosis induced reductive glutamine metabolism (Supplementary Fig. 10). These data demonstrate that glutamine-dependent reductive carboxylation is a common cellular response to impaired mitochondrial metabolism.

Glutamine-dependent reductive carboxylation has been described previously as a minor source of isocitrate/citrate and lipogenic carbon in mammalian cells12,13,1820. In Plasmodium falciparum, a unicellular protozoan with limited respiration, the pathway is a major source of citrate and acetyl units21. We show that this pathway can also function as the predominant metabolic strategy to produce lipids for cancer cell growth, and can be induced acutely during ETC inhibition. We speculate that reductive carboxylation is stimulated by a disturbance in the redox ratio of the mitochondria caused by ETC impairment, decreasing the NAD+/NADH ratio and rendering oxidative function of the CAC less efficient. This ratio could be dissipated in part by NAD(P)-transhydrogenases, which transfer reducing equivalents from NADH to NADPH, and this in turn may drive NADPH-dependent reductive carboxylation by IDH1 and IDH2. This redirection of the CAC extends the versatility of glutamine metabolism in cancer cell growth. In cells with normal mitochondria, glutamine oxidation is frequently the major source of anaplerosis, providing most of the carbon to pools of CAC intermediates and facilitating production of macromolecular precursors in the mitochondria22. Glutamine-dependent reductive carboxylation enables glutamine to retain this status as a growth-promoting nutrient even when mitochondrial metabolism is impaired. Therefore, during malignant transformation the acquisition of somatic mutations that impair mitochondrial function and stimulate aerobic glycolysis (the Warburg effect) does not diminish the importance of glutamine metabolism or of the mitochondria themselves for tumor cell proliferation.


Methods Summary

143Bwt and 143Bcytb and UOK262 cells were cultured as described9,15. MEFs were cultured in Dulbecco’s Modified Eagle Medium (DMEM) with 10% fetal bovine serum (FBS, Hyclone), penicillin/streptomycin and 6mM L-glutamine. Cell growth was monitored in sub-confluent cultures by trypsinizing and counting with a hemacytometer. Glucose, lactate, and glutamine were measured as described23. Isotopic labeling was performed in DMEM with 10% dialyzed FBS supplemented with either 15mM D-[U-13C]glucose or 2mM L-[U-13C]glutamine. Aqueous metabolites were analyzed using an Agilent 6970 gas chromatograph and an Agilent 5973 mass selective detector. To determine relative metabolite abundance across samples, the area of the total ion current peak for the relevant metabolite was compared to that of an internal standard (2-oxobutyrate) and normalized for protein content. Analysis of 13C enrichment and mass isotopomer distribution was performed as published11,24. For radioisotope lipid synthesis assays, cells were cultured for 18 hours in complete medium supplemented with 3H2O or 14C tracers (Perkin Elmer). Lipids were extracted and analyzed as described3. For lipid synthesis experiments using NMR, cells were plated in 10-cm dishes and allowed to proliferate exponentially in medium containing D[U-13C]glucose and unlabeled glutamine, or unlabeled glucose and L[U-13C]glutamine until two confluent 15-cm dishes were obtained. Lipids were then extracted and analyzed by 13C NMR as described3. Gene silencing was performed using commercial small interfering RNAs (Thermo) directed against IDH1, IDH2 or IDH3. Cells were transfected with DharmaFECT transfection reagent (Thermo) and protein abundance was examined after 72 hours using western blots with commercial antibodies (Santa Cruz Biotechnology). Cells were incubated with L[U-13C]glutamine for two hours prior to extraction of metabolites for mass isotopomer distribution analysis. Stable silencing used lentiviral shRNAs from the Mission shRNA pLKO.1-puro library (Sigma). Additional details are in the online Methods.



Notes

FN2Supplementary Information is linked to the online version of the paper at www.nature.com/nature.

FN3Author Contributions. A.R.M., W.W.W., N.S.C. and R.J.D. designed the research. A.R.M., W.W.W., L.B.S., E.S.J., T.C. and P-H.C. performed the experiments. A.R.M., W.W.W., L.B.S., E.S.J., P-S.C., T.C., N.S.C. and R.J.D. analyzed the data. Y.Y. and W.M.L. provided the FH-deficient (UOK262) cells. A.R.M., N.S.C. and R.J.D. wrote the paper.

FN4None of the authors have competing financial interests to declare. Reprints and permissions information is available at www.nature.com/reprints.

Kosaku Uyeda and members of the DeBerardinis and Chandel laboratories provided critical assessment of the data, and Jessica Sudderth and Chendong Yang provided experimental assistance. We thank Carlos Moraes and I.F.M. de Coo for the 143Bwt and 143Bcytb cell lines, Immo E. Scheffler for CCL16-B2 cells and Takao Yagi for CCL16-NDI1 cells. This work was supported by grants to R.J.D. from the N.I.H. (K08DK072565, R01CA157996, and RR02584), the Cancer Prevention and Research Institute of Texas (CPRIT, HIRP100437) and the Robert A. Welch Foundation (I1733); to N.S.C. from the N.I.H. (R01CA123067), the LUNGevity Foundation and a Consortium of Independent Lung Health Organizations convened by Respiratory Health Association of Metropolitan Chicago; and to E.S.J. by an N.I.H. grant (DK078933). The work was also supported by the Intramural Research Program of the N.I.H., National Cancer Institute Center for Cancer Research. N.I.H. training grants supported A.R.M. (5T32GM083831), W.W.W. (T32CA009560) and L.B.S. (T32GM008061). T.C. was supported by a CPRIT training grant.


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