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营养应激重塑癌细胞代谢。

Nutrient stress revamps cancer cell metabolism.

作者信息

Moscat Jorge, Richardson Adam, Diaz-Meco Maria T

机构信息

Sanford-Burnham Medical Research Institute, La Jolla, CA 92037, USA.

出版信息

Cell Res. 2015 May;25(5):537-8. doi: 10.1038/cr.2015.38. Epub 2015 Mar 31.

DOI:10.1038/cr.2015.38
PMID:25828529
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4423079/
Abstract

Efforts to identify new therapeutic targets in cancer primarily focused on oncogenes and tumor suppressor genes, and their mechanisms of action. However, there is an emerging alternative strategy that involves identification of target proteins that are not encoded by oncogenes, but are, nonetheless, required to accommodate cancer-specific stresses.

摘要

在癌症中识别新治疗靶点的努力主要集中在癌基因和肿瘤抑制基因及其作用机制上。然而,一种新出现的替代策略涉及识别并非由癌基因编码,但却是适应癌症特异性应激所必需的靶蛋白。

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1
Nutrient stress revamps cancer cell metabolism.营养应激重塑癌细胞代谢。
Cell Res. 2015 May;25(5):537-8. doi: 10.1038/cr.2015.38. Epub 2015 Mar 31.
2
Autophagy, stress, and cancer metabolism: what doesn't kill you makes you stronger.自噬、应激与癌症代谢:杀不死你的会让你更强大。
Cold Spring Harb Symp Quant Biol. 2011;76:389-96. doi: 10.1101/sqb.2012.76.011015. Epub 2012 Mar 22.
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Autophagy: an adaptive metabolic response to stress shaping the antitumor immunity.自噬:一种适应代谢应激的反应,可塑造抗肿瘤免疫。
Biochem Pharmacol. 2014 Nov 1;92(1):31-42. doi: 10.1016/j.bcp.2014.07.006. Epub 2014 Jul 17.
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14-3-3 proteins as potential oncogenes.14-3-3蛋白作为潜在的癌基因。
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5
[Adaptive response of cancer cells to metabolic stress].[癌细胞对代谢应激的适应性反应]
Nihon Rinsho. 2014 Jun;72(6):1058-62.
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Regulation of cancer metabolism by oncogenes and tumor suppressors.癌基因与肿瘤抑制因子对癌症代谢的调控。
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[P53 "teams up" with the energy metabolism of tumors].[P53与肿瘤的能量代谢“联手”]
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Semin Oncol. 2006 Aug;33(4):513-20. doi: 10.1053/j.seminoncol.2006.04.013.

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HIF: a master regulator of nutrient availability and metabolic cross-talk in the tumor microenvironment.缺氧诱导因子(HIF):肿瘤微环境中营养可用性和代谢串扰的主要调节因子。
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本文引用的文献

1
cMyc-mediated activation of serine biosynthesis pathway is critical for cancer progression under nutrient deprivation conditions.cMyc介导的丝氨酸生物合成途径激活在营养剥夺条件下对癌症进展至关重要。
Cell Res. 2015 Apr;25(4):429-44. doi: 10.1038/cr.2015.33. Epub 2015 Mar 20.
2
Metabolic reprogramming of stromal fibroblasts through p62-mTORC1 signaling promotes inflammation and tumorigenesis.通过 p62-mTORC1 信号对基质成纤维细胞进行代谢重编程可促进炎症和肿瘤发生。
Cancer Cell. 2014 Jul 14;26(1):121-135. doi: 10.1016/j.ccr.2014.05.004. Epub 2014 Jul 4.
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Quantitative flux analysis reveals folate-dependent NADPH production.定量通量分析揭示了叶酸依赖性 NADPH 的产生。
Nature. 2014 Jun 12;510(7504):298-302. doi: 10.1038/nature13236. Epub 2014 May 4.
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Control of nutrient stress-induced metabolic reprogramming by PKCζ in tumorigenesis.PKCζ 调控营养应激诱导的代谢重编程在肿瘤发生中的作用。
Cell. 2013 Jan 31;152(3):599-611. doi: 10.1016/j.cell.2012.12.028.
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Serine is a natural ligand and allosteric activator of pyruvate kinase M2.丝氨酸是丙酮酸激酶 M2 的天然配体和别构激活剂。
Nature. 2012 Nov 15;491(7424):458-462. doi: 10.1038/nature11540. Epub 2012 Oct 14.
6
Pyruvate kinase M2 promotes de novo serine synthesis to sustain mTORC1 activity and cell proliferation.丙酮酸激酶 M2 促进从头合成丝氨酸以维持 mTORC1 活性和细胞增殖。
Proc Natl Acad Sci U S A. 2012 May 1;109(18):6904-9. doi: 10.1073/pnas.1204176109. Epub 2012 Apr 16.
7
Phosphoglycerate dehydrogenase diverts glycolytic flux and contributes to oncogenesis.磷酸甘油酸脱氢酶改变糖酵解通量并促进肿瘤发生。
Nat Genet. 2011 Jul 31;43(9):869-74. doi: 10.1038/ng.890.
8
Functional genomics reveal that the serine synthesis pathway is essential in breast cancer.功能基因组学揭示丝氨酸合成途径在乳腺癌中是必不可少的。
Nature. 2011 Aug 18;476(7360):346-50. doi: 10.1038/nature10350.
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.
10
An evaluation of tumor oxygenation and gene expression in patients with early stage non-small cell lung cancers.早期非小细胞肺癌患者肿瘤氧合及基因表达的评估
Clin Cancer Res. 2006 Mar 1;12(5):1507-14. doi: 10.1158/1078-0432.CCR-05-2049.