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本文引用的文献

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The Hippo pathway and human cancer.Hippo 通路与人类癌症。
Nat Rev Cancer. 2013 Apr;13(4):246-57. doi: 10.1038/nrc3458. Epub 2013 Mar 7.
2
Quantitative phosphoproteomics reveal mTORC1 activates de novo pyrimidine synthesis.定量磷酸化蛋白质组学揭示 mTORC1 激活从头嘧啶合成。
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Regulation of glycolysis by Pdk functions as a metabolic checkpoint for cell cycle quiescence in hematopoietic stem cells.PDK 对糖酵解的调节可作为造血干细胞细胞周期静止的代谢检查点。
Cell Stem Cell. 2013 Jan 3;12(1):49-61. doi: 10.1016/j.stem.2012.10.011.
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Regulation of mTORC1 by the Rag GTPases is necessary for neonatal autophagy and survival.雷帕霉素靶蛋白复合物 1(mTORC1)的 Rag GTPases 调控对于新生儿自噬和存活是必需的。
Nature. 2013 Jan 31;493(7434):679-83. doi: 10.1038/nature11745. Epub 2012 Dec 23.
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Mitofusin 1 is degraded at G2/M phase through ubiquitylation by MARCH5.线粒体融合蛋白 1 在 G2/M 期通过 MARCH5 的泛素化降解。
Cell Div. 2012 Dec 20;7(1):25. doi: 10.1186/1747-1028-7-25.
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AMP-activated protein kinase: a target for drugs both ancient and modern.AMP激活的蛋白激酶:古今药物的作用靶点。
Chem Biol. 2012 Oct 26;19(10):1222-36. doi: 10.1016/j.chembiol.2012.08.019.
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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.
8
Mitochondrial defect drives non-autonomous tumour progression through Hippo signalling in Drosophila.线粒体缺陷通过 Hippo 信号通路在果蝇中非自主性地驱动肿瘤进展。
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9
Metabolic checkpoints in activated T cells.激活 T 细胞中的代谢检查点。
Nat Immunol. 2012 Oct;13(10):907-15. doi: 10.1038/ni.2386. Epub 2012 Sep 18.
10
Ragulator is a GEF for the rag GTPases that signal amino acid levels to mTORC1.Ragulator 是 Rag GTPases 的鸟苷酸交换因子 (GEF),可将氨基酸水平信号传递给 mTORC1。
Cell. 2012 Sep 14;150(6):1196-208. doi: 10.1016/j.cell.2012.07.032.

细胞周期的代谢调控。

Metabolic regulation of the cell cycle.

机构信息

Center for Molecular Medicine, National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, MD 20892, USA; Department of Life Science, Division of Life and Pharmaceutical Sciences, Ewha Womans University, 11-1 Daehyun-Dong Seodaemoon-Gu, Seoul, South Korea.

出版信息

Curr Opin Cell Biol. 2013 Dec;25(6):724-9. doi: 10.1016/j.ceb.2013.07.002. Epub 2013 Jul 24.

DOI:10.1016/j.ceb.2013.07.002
PMID:23890700
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3836844/
Abstract

There is a growing appreciation that metabolic signals are integrated and coupled to cell cycle progression. However, the molecular wiring that connects nutrient availability, biosynthetic intermediates and energetic balance to the core cell cycle machinery remains incompletely understood. In this review, we explore the recent progress in this area with particular emphasis on how nutrient and energetic status is sensed within the cell to ultimately regulate cell growth and division. The role these pathways play in normal cell function including stem cell biology is also discussed. Furthermore, we describe the growing appreciation that dysregulation of these pathways might contribute to a variety of pathological conditions including metabolic diseases and tumor formation.

摘要

人们越来越认识到,代谢信号是相互整合和耦合的,与细胞周期的进展有关。然而,将营养物质的可用性、生物合成中间体和能量平衡与核心细胞周期机制联系起来的分子连接仍然不完全清楚。在这篇综述中,我们探讨了这一领域的最新进展,特别强调了细胞内如何感知营养和能量状态,最终调节细胞生长和分裂。还讨论了这些途径在正常细胞功能中的作用,包括干细胞生物学。此外,我们描述了人们越来越认识到,这些途径的失调可能导致多种病理状况,包括代谢疾病和肿瘤形成。