The emerging role and targetability of the TCA cycle in cancer metabolism

被引:354
作者
Anderson, Nicole M. [1 ,2 ]
Mucka, Patrick [3 ,4 ]
Kern, Joseph G. [5 ]
Feng, Hui [3 ,4 ]
机构
[1] Univ Penn, Abramson Family Canc Res Inst, Philadelphia, PA 19104 USA
[2] Univ Penn, Perelman Sch Med, Philadelphia, PA 19104 USA
[3] Boston Univ, Sch Med, Ctr Canc Res, Sect Hematol & Med Oncol,Dept Pharmacol, Boston, MA 02118 USA
[4] Boston Univ, Sch Med, Ctr Canc Res, Sect Hematol & Med Oncol,Dept Med, Boston, MA 02118 USA
[5] Boston Univ, Sch Med, Program Biomed Sci, Boston, MA 02118 USA
基金
美国国家卫生研究院;
关键词
glutaminolysis; the TCA cycle; cancer metabolism; glycolysis; GASTROINTESTINAL STROMAL TUMORS; RENAL-CELL-CANCER; SUCCINATE-DEHYDROGENASE SUBUNIT; ACUTE MYELOID-LEUKEMIA; FATTY-ACID SYNTHASE; ATP CITRATE LYASE; HYPOXIA-INDUCIBLE FACTORS; COMPLEX-II GENE; HEREDITARY LEIOMYOMATOSIS; GERMLINE MUTATIONS;
D O I
10.1007/s13238-017-0451-1
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The tricarboxylic acid (TCA) cycle is a central route for oxidative phosphorylation in cells, and fulfills their bioenergetic, biosynthetic, and redox balance requirements. Despite early dogma that cancer cells bypass the TCA cycle and primarily utilize aerobic glycolysis, emerging evidence demonstrates that certain cancer cells, especially those with deregulated oncogene and tumor suppressor expression, rely heavily on the TCA cycle for energy production and macromolecule synthesis. As the field progresses, the importance of aberrant TCA cycle function in tumorigenesis and the potentials of applying small molecule inhibitors to perturb the enhanced cycle function for cancer treatment start to evolve. In this review, we summarize current knowledge about the fuels feeding the cycle, effects of oncogenes and tumor suppressors on fuel and cycle usage, common genetic alterations and deregulation of cycle enzymes, and potential therapeutic opportunities for targeting the TCA cycle in cancer cells. With the application of advanced technology and in vivo model organism studies, it is our hope that studies of this previously overlooked biochemical hub will provide fresh insights into cancer metabolism and tumorigenesis, subsequently revealing vulnerabilities for therapeutic interventions in various cancer types.
引用
收藏
页码:216 / 237
页数:22
相关论文
共 189 条
  • [1] Acquired mutations in the genes encoding IDH1 and IDH2 both are recurrent aberrations in acute myeloid leukemia: prevalence and prognostic value
    Abbas, Saman
    Lugthart, Sanne
    Kavelaars, Francois G.
    Schelen, Anita
    Koenders, Jasper E.
    Zeilemaker, Annelieke
    van Putten, Wim J. L.
    Rijneveld, Anita W.
    Lowenberg, Bob
    Valk, Peter J. M.
    [J]. BLOOD, 2010, 116 (12) : 2122 - 2126
  • [2] Transcriptional regulation and transformation by MYC proteins
    Adhikary, S
    Eilers, M
    [J]. NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2005, 6 (08) : 635 - 645
  • [3] METABOLISM AND ACTION OF AMINO-ACID ANALOG ANTICANCER AGENTS
    AHLUWALIA, GS
    GREM, JL
    HAO, Z
    COONEY, DA
    [J]. PHARMACOLOGY & THERAPEUTICS, 1990, 46 (02) : 243 - 271
  • [4] Citric Acid Cycle and Role of its Intermediates in Metabolism
    Akram, Muhammad
    [J]. CELL BIOCHEMISTRY AND BIOPHYSICS, 2014, 68 (03) : 475 - 478
  • [5] Differential Aspartate Usage Identifies a Subset of Cancer Cells Particularly Dependent on OGDH
    Allen, Eric L.
    Ulanet, Danielle B.
    Pirman, David
    Mahoney, Christopher E.
    Coco, John
    Si, Yaguang
    Chen, Ying
    Huang, Lingling
    Ren, Jinmin
    Choe, Sung
    Clasquin, Michelle F.
    Artin, Erin
    Fan, Zi Peng
    Cianchetta, Giovanni
    Murtie, Joshua
    Dorsch, Marion
    Jin, Shengfang
    Smolen, Gromoslaw A.
    [J]. CELL REPORTS, 2016, 17 (03): : 876 - 890
  • [6] IDH1 and IDH2 mutations are frequent events in central chondrosarcoma and central and periosteal chondromas but not in other mesenchymal tumours
    Amary, M. Fernanda
    Bacsi, Krisztian
    Maggiani, Francesca
    Damato, Stephen
    Halai, Dina
    Berisha, Fitim
    Pollock, Robin
    O'Donnell, Paul
    Grigoriadis, Anita
    Diss, Tim
    Eskandarpour, Malihe
    Presneau, Nadege
    Hogendoorn, Pancras C. W.
    Futreal, Andrew
    Tirabosco, Roberto
    Flanagan, Adrienne M.
    [J]. JOURNAL OF PATHOLOGY, 2011, 224 (03) : 334 - 343
  • [7] The TCA cycle transferase DLST is important for MYC-mediated leukemogenesis
    Anderson, N. M.
    Li, D.
    Peng, H. L.
    Laroche, F. J. F.
    Mansour, M. R.
    Gjini, E.
    Aioub, M.
    Helman, D. J.
    Roderick, J. E.
    Cheng, T.
    Harrold, I.
    Samaha, Y.
    Meng, L.
    Amsterdam, A.
    Neuberg, D. S.
    Denton, T. T.
    Sanda, T.
    Kelliher, M. A.
    Singh, A.
    Look, A. T.
    Feng, H.
    [J]. LEUKEMIA, 2016, 30 (06) : 1365 - 1374
  • [8] Hereditary leiomyomatosis and renal cell cancer syndrome: identification and clinical characterization of a novel mutation in the FH gene in a Colombian family
    Arenas Valencia, Carolina
    Rodriguez Lopez, Martha Lucia
    Cardona Barreto, Andrea Yimena
    Garavito Rodriguez, Edgar
    Arteaga Diaz, Clara Eugenia
    [J]. FAMILIAL CANCER, 2017, 16 (01) : 117 - 122
  • [9] Aspuria PJP, 2014, CANCER METAB, V2, DOI 10.1186/2049-3002-2-21
  • [10] Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma
    Astuti, D
    Latif, F
    Dallol, A
    Dahia, PLM
    Douglas, F
    George, E
    Sköldberg, F
    Husebye, ES
    Eng, C
    Maher, ER
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (01) : 49 - 54