[1] Louis DN, Ohgaki H,Wiestler OD, et al.The 2007WHO classification of tumours of the central nervous system[J].Acta Neuropathol,2007,114(2):97-109. [2] Hess KR, Broglio KR, Bondy ML.Adult glioma incidence trends in the United States, 1977-2000[J].Cancer,2004,101(10):2293-2299. [3] Norden AD, Wen PY. Glioma therapy in adults[J].Neurologist,2006,12(6):279-292. [4] Behin A,Hoang-Xuan K,Delattre JY.Primary brain tumours in adults[J].Lancet,2003,361(9354):323-331. [5] DeAngelis LM. Brain tumors[J].N Engl J Med,2001,344(2):114-123. [6] Garber K. Energy deregulation: Licensing tumor to grow[J].Science,2006,312 (5777):1158-1159. [7] Boros LG, Puigjaner J, Schirmer WJ,et al.Oxythiamine and dehydroepiandrosterone inhibit the nonoxidative synthesis of ribose and tumor cell proliferation[J]. Cancer Res,1997,57(19):4242-4248. [8] Coy JF,Dressler D,Wilde J,et al.Mutations in the transketolase-like gene TKTL1:clinical implications for neurodegenerative diseases, diabetes and cancer[J]. Clin Lab,2005,51(5/6):257-273. [9] Langbein S,Zerilli M,Zur Hausen A,et al.Expression of transketolase TKTL1 predicts colon and urothelial cancer patient survival: Warburg effect reinterpreted[J].Br J Cancer,2006,94(4):578-585. [10]Staiger WI, Coy JF, Grobholz R,et al.Expression of the mutated transketolase TKTL1, a molecular marker in gastric cancer[J].Oncol Rep,2006,16(4):657-661. [11]Langbein S, Frederiks WM, zur Hausen A, et al.Metastasis is promoted by a bioenergetic switch: new targets for progressive renal cell cancer[J].Int J Cancer,2008,122(11):2422-2428. [12]VaLker HU,Scheich M,Schmausser B, et al. Overexpression of transketolase TKTL1 is associated with shorter surviva1 in laryngeal squamous cell carcinomas[J].Eur Arch Otorhinolar yngol,2007,264(12):1431-1436. [13]Schwaab J, Horisberger K, Ströbel P, et al.Expression of Transketolase like gene1 (TKTL1) predicts disease-free survival in patients with locally advanced rectal cancer receiving neoadjuvant chemoradiotherapy[J].BMC Cancer,2011,11:363-372. [14] Sun W,Liu Y,Glazer CA,et al. TKTL1 is activated by promoter hypomethylation and contributes to head and neck squamous cell carcinoma carcinogenesis through increased aerobic glycolysis and HIF1{alpha} stabilization[J].Clin Cancer Res, 2010,16(3): 857-866. [15]Wenyue S,Yan L,Chad AG,et al. TKTL1 is activated by promoter hypomethylation and contributes to head and neck squamous cell carcinoma carcinogenesis via increased aerobic glycolysis and HIF1α stabilization[J].Clin Cancer Res, 2010,16(3):857-866. [16]Atsumi T,Chesney J,Metz C,et al.High expression of inducible 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase(iPFK-2; PFKFB3) in human cancers[J].Cancer Res, 2002,62(20):5881-5887. [17]Telang S,Yalcin A,Clem AL,et al.Ras transformation requires metabolic control by 6-phosphofructo-2-kinase[J]. Oncogene, 2006,25(55):7225-7234. [18]Minchenko A,Leshchinsky I,Opentanova I,et al. Hypoxia-inducible factor-1-mediated expression of the 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase-3(PFKFB3) gene. Its possible role in the Warburg effect[J].J Biol Chem, 2002,277(8): 6183-6187. [19]Lu H,Dalgard CL,Mohyeldin A,et al. Reversible inactivation of HIF-1 prolyl hydroxylases allows cell metabolism to control basal HIF-1[J].J Biol Chem,2005,280(51): 41928-41939. [20]Baker LC, Boult JK, Walker-Samuel S, et al.The HIF-pathway inhibitor NSC-134754 induces metabolic changes and anti-tumour activity while maintaining vascular function[J]. Br J Cancer, 2012,106(10):1638-1647. [21]Sarah SR.Microenvironment:making connections[J].Nat Rev Cancer,2013,13(4):222-223. |