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本文引用的文献

1
Analysis of tumor metabolism reveals mitochondrial glucose oxidation in genetically diverse human glioblastomas in the mouse brain in vivo.肿瘤代谢分析揭示了体内小鼠脑内遗传多样化的人类胶质母细胞瘤中线粒体葡萄糖氧化。
Cell Metab. 2012 Jun 6;15(6):827-37. doi: 10.1016/j.cmet.2012.05.001.
2
Metabolism of [U-13 C]glucose in human brain tumors in vivo.体内[U-13 C]葡萄糖在人脑肿瘤中的代谢。
NMR Biomed. 2012 Nov;25(11):1234-44. doi: 10.1002/nbm.2794. Epub 2012 Mar 15.
3
Reductive glutamine metabolism by IDH1 mediates lipogenesis under hypoxia.IDH1 介导的还原性谷氨酰胺代谢在低氧条件下促进脂肪生成。
Nature. 2011 Nov 20;481(7381):380-4. doi: 10.1038/nature10602.
4
Reductive carboxylation supports growth in tumour cells with defective mitochondria.还原羧化作用为线粒体功能缺陷的肿瘤细胞生长提供支持。
Nature. 2011 Nov 20;481(7381):385-8. doi: 10.1038/nature10642.
5
Stochastic state transitions give rise to phenotypic equilibrium in populations of cancer cells.随机状态转变导致癌细胞群体中的表型平衡。
Cell. 2011 Aug 19;146(4):633-44. doi: 10.1016/j.cell.2011.07.026.
6
Otto Warburg's contributions to current concepts of cancer metabolism.奥托·瓦尔堡对当前癌症代谢概念的贡献。
Nat Rev Cancer. 2011 May;11(5):325-37. doi: 10.1038/nrc3038. Epub 2011 Apr 14.
7
New strategies in the molecular targeting of glioblastoma: how do you hit a moving target?脑胶质瘤的分子靶向新策略:如何击中移动的目标?
Clin Cancer Res. 2011 Jan 1;17(1):6-11. doi: 10.1158/1078-0432.CCR-09-2268.
8
Metabolic modulation of glioblastoma with dichloroacetate.二氯乙酸对神经胶质瘤的代谢调节。
Sci Transl Med. 2010 May 12;2(31):31ra34. doi: 10.1126/scitranslmed.3000677.
9
Understanding the Warburg effect: the metabolic requirements of cell proliferation.理解瓦伯格效应:细胞增殖的代谢需求。
Science. 2009 May 22;324(5930):1029-33. doi: 10.1126/science.1160809.

活跃的代谢模式改变:线粒体葡萄糖氧化为神经胶质瘤生长供能。

HOT models in flux: mitochondrial glucose oxidation fuels glioblastoma growth.

机构信息

Departments of Pathology and Laboratory Medicine and Molecular and Medical Pharmacology, The David Geffen UCLA School of Medicine, Los Angeles, CA 90095, USA.

出版信息

Cell Metab. 2012 Jun 6;15(6):789-90. doi: 10.1016/j.cmet.2012.05.004.

DOI:10.1016/j.cmet.2012.05.004
PMID:22682216
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3376384/
Abstract

Cancer cells in culture obtain ATP and biosynthetic precursors primarily by aerobic glycolysis, not by mitochondrial glucose oxidation. In this issue of Cell Metabolism, Marin-Valencia et al. (2012) demonstrate that glioblastoma, an aggressive and, in culture, highly glycolytic cancer, primarily uses glucose oxidation to meet energetic and biosynthetic demands in vivo.

摘要

在培养的癌细胞中,细胞主要通过有氧糖酵解而非线粒体葡萄糖氧化获取三磷酸腺苷(ATP)和生物合成前体。在本期《细胞代谢》中,Marin-Valencia 等人(2012)证明,神经胶质瘤(一种侵袭性的、在培养中高度糖酵解的癌症)在体内主要利用葡萄糖氧化来满足能量和生物合成需求。