Metabolic Syndromes and Malignant Transformation: Where the Twain Shall Meet

被引:2
作者
Bhagwat, Neha [1 ,2 ]
Levine, Ross L. [1 ,2 ,3 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Human Oncol & Pathogenesis Program, New York, NY 10065 USA
[2] Mem Sloan Kettering Canc Ctr, Gerstner Sloan Kettering Sch Biomed Sci, New York, NY 10065 USA
[3] Mem Sloan Kettering Canc Ctr, Leukemia Serv, Dept Med, New York, NY 10065 USA
关键词
D-2-HYDROXYGLUTARIC ACIDURIA; IDH2; MUTATIONS; LEUKEMIA; COMPLEX; CANCER; GENE;
D O I
10.1126/scitranslmed.3001669
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Recurrent somatic mutations in the isocitrate dehydrogenase 1 (IDH1) and IDH2 genes that result in the accumulation of D-2-hydroxyglutarate (D-2-HG) have been identified in malignant gliomas and in acute myeloid leukemia (AML). However, the function of this metabolite in normal and malignant tissues remains uncertain. A report in the current issue of Science describes a germline IDH2 mutation in a subset of patients with a rare metabolic disorder-D-2-hydroxyglutaric aciduria-that is similar to mutations seen in cancer patients. These observations further elucidate the effects of IDH mutations on normal and malignant cells.
引用
收藏
页数:3
相关论文
共 16 条
  • [1] Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma
    Baysal, BE
    Ferrell, RE
    Willett-Brozick, JE
    Lawrence, EC
    Myssiorek, D
    Bosch, A
    van der Mey, A
    Taschner, PEM
    Rubinstein, WS
    Myers, EN
    Richard, CW
    Cornelisse, CJ
    Devilee, P
    Devlin, B
    [J]. SCIENCE, 2000, 287 (5454) : 848 - 851
  • [2] Cancer-associated IDH1 mutations produce 2-hydroxyglutarate
    Dang, Lenny
    White, David W.
    Gross, Stefan
    Bennett, Bryson D.
    Bittinger, Mark A.
    Driggers, Edward M.
    Fantin, Valeria R.
    Jang, Hyun Gyung
    Jin, Shengfang
    Keenan, Marie C.
    Marks, Kevin M.
    Prins, Robert M.
    Ward, Patrick S.
    Yen, Katharine E.
    Liau, Linda M.
    Rabinowitz, Joshua D.
    Cantley, Lewis C.
    Thompson, Craig B.
    Heiden, Matthew G. Vander
    Su, Shinsan M.
    [J]. NATURE, 2009, 462 (7274) : 739 - U52
  • [3] Cancer-associated metabolite 2-hydroxyglutarate accumulates in acute myelogenous leukemia with isocitrate dehydrogenase 1 and 2 mutations
    Gross, Stefan
    Cairns, Rob A.
    Minden, Mark D.
    Driggers, Edward M.
    Bittinger, Mark A.
    Jang, Hyun Gyung
    Sasaki, Masato
    Jin, Shengfang
    Schenkein, David P.
    Su, Shinsan M.
    Dang, Lenny
    Fantin, Valeria R.
    Mak, Tak W.
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 2010, 207 (02) : 339 - 344
  • [4] Targeting of HIF-α to the von Hippel-Lindau ubiquitylation complex by O2-regulated prolyl hydroxylation
    Jaakkola, P
    Mole, DR
    Tian, YM
    Wilson, MI
    Gielbert, J
    Gaskell, SJ
    von Kriegsheim, A
    Hebestreit, HF
    Mukherji, M
    Schofield, CJ
    Maxwell, PH
    Pugh, CW
    Ratcliffe, PJ
    [J]. SCIENCE, 2001, 292 (5516) : 468 - 472
  • [5] IDH2 Mutations in Patients with D-2-Hydroxyglutaric Aciduria
    Kranendijk, Martijn
    Struys, Eduard A.
    van Schaftingen, Emile
    Gibson, K. Michael
    Kanhai, Warsha A.
    van der Knaap, Marjo S.
    Amiel, Jeanne
    Buist, Neil R.
    Das, Anibh M.
    de Klerk, Johannis B.
    Feigenbaum, Annette S.
    Grange, Dorothy K.
    Hofstede, Floris C.
    Holme, Elisabeth
    Kirk, Edwin P.
    Korman, Stanley H.
    Morava, Eva
    Morris, Andrew
    Smeitink, Jan
    Sukhai, Ram N.
    Vallance, Hilary
    Jakobs, Cornelis
    Salomons, Gajja S.
    [J]. SCIENCE, 2010, 330 (6002) : 336 - 336
  • [6] D-2-hydroxyglutaric acid induces oxidative stress in cerebral cortex of young rats
    Latini, A
    Scussiato, K
    Rosa, RB
    Llesuy, S
    Belló-Klein, A
    Dutra-Filho, CS
    Wajner, M
    [J]. EUROPEAN JOURNAL OF NEUROSCIENCE, 2003, 17 (10) : 2017 - 2022
  • [7] Recurring Mutations Found by Sequencing an Acute Myeloid Leukemia Genome
    Mardis, Elaine R.
    Ding, Li
    Dooling, David J.
    Larson, David E.
    McLellan, Michael D.
    Chen, Ken
    Koboldt, Daniel C.
    Fulton, Robert S.
    Delehaunty, Kim D.
    McGrath, Sean D.
    Fulton, Lucinda A.
    Locke, Devin P.
    Magrini, Vincent J.
    Abbott, Rachel M.
    Vickery, Tammi L.
    Reed, Jerry S.
    Robinson, Jody S.
    Wylie, Todd
    Smith, Scott M.
    Carmichael, Lynn
    Eldred, James M.
    Harris, Christopher C.
    Walker, Jason
    Peck, Joshua B.
    Du, Feiyu
    Dukes, Adam F.
    Sanderson, Gabriel E.
    Brummett, Anthony M.
    Clark, Eric
    McMichael, Joshua F.
    Meyer, Rick J.
    Schindler, Jonathan K.
    Pohl, Craig S.
    Wallis, John W.
    Shi, Xiaoqi
    Lin, Ling
    Schmidt, Heather
    Tang, Yuzhu
    Haipek, Carrie
    Wiechert, Madeline E.
    Ivy, Jolynda V.
    Kalicki, Joelle
    Elliott, Glendoria
    Ries, Rhonda E.
    Payton, Jacqueline E.
    Westervelt, Peter
    Tomasson, Michael H.
    Watson, Mark A.
    Baty, Jack
    Heath, Sharon
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2009, 361 (11) : 1058 - 1066
  • [8] The tumour suppressor protein VHL targets hypoxia-inducible factors for oxygen-dependent proteolysis
    Maxwell, PH
    Wiesener, MS
    Chang, GW
    Clifford, SC
    Vaux, EC
    Cockman, ME
    Wykoff, CC
    Pugh, CW
    Maher, ER
    Ratcliffe, PJ
    [J]. NATURE, 1999, 399 (6733) : 271 - 275
  • [9] An integrated genomic analysis of human glioblastoma Multiforme
    Parsons, D. Williams
    Jones, Sian
    Zhang, Xiaosong
    Lin, Jimmy Cheng-Ho
    Leary, Rebecca J.
    Angenendt, Philipp
    Mankoo, Parminder
    Carter, Hannah
    Siu, I-Mei
    Gallia, Gary L.
    Olivi, Alessandro
    McLendon, Roger
    Rasheed, B. Ahmed
    Keir, Stephen
    Nikolskaya, Tatiana
    Nikolsky, Yuri
    Busam, Dana A.
    Tekleab, Hanna
    Diaz, Luis A., Jr.
    Hartigan, James
    Smith, Doug R.
    Strausberg, Robert L.
    Marie, Suely Kazue Nagahashi
    Shinjo, Sueli Mieko Oba
    Yan, Hai
    Riggins, Gregory J.
    Bigner, Darell D.
    Karchin, Rachel
    Papadopoulos, Nick
    Parmigiani, Giovanni
    Vogelstein, Bert
    Velculescu, Victor E.
    Kinzler, Kenneth W.
    [J]. SCIENCE, 2008, 321 (5897) : 1807 - 1812
  • [10] D-2-Hydroxyglutaric aciduria: Unravelling the biochemical pathway and the genetic defect
    Struys, EA
    [J]. JOURNAL OF INHERITED METABOLIC DISEASE, 2006, 29 (01) : 21 - 29