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癌症干细胞的核重编程:用致癌代谢物破坏细胞身份的表观遗传密码。

Nuclear reprogramming of cancer stem cells: Corrupting the epigenetic code of cell identity with oncometabolites.

作者信息

Menendez Javier A, Alarcón Tomás

机构信息

ProCURE (Program Against Cancer Therapeutic Resistance), Metabolism and Cancer Group, Catalan Institute of Oncology, Girona, Catalonia, Spain; Molecular Oncology Group, Girona Biomedical Research Institute (IDIBGI), Salt, Catalonia, Spain.

Computational & Mathematical Biology Research Group, Center de Recerca Matemàtica, Barcelona, Catalonia, Spain; ICREA (Institució Catalana d'Estudis i Recerca Avançats), Barcelona, Spain; Departament de Matemàtiques, Universitat Autónoma de Barcelona, Barcelona, Spain; Barcelona Graduate School of Mathematics (BGSMath), Barcelona, Spain.

出版信息

Mol Cell Oncol. 2016 Mar 28;3(6):e1160854. doi: 10.1080/23723556.2016.1160854. eCollection 2016.

DOI:10.1080/23723556.2016.1160854
PMID:28090573
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5160399/
Abstract

Generation of cancer stem cell (CSC)-like cells might occur through metabolic corruption of the epigenetic codes that govern cell identity. We recently identified how archetypal oncometabolites, without altering the baseline expression of endogenous stem cell maintenance genes but endowing cells with epigenetic states refractory to differentiation, considerably enhance the global kinetic efficiency of nuclear reprogramming processes that generate CSC-like states . This study highlights that metabolo-epigenetic axes of communication can direct the development and maintenance of CSCs during the natural history of cancer diseases.

摘要

癌症干细胞(CSC)样细胞的产生可能是通过调控细胞身份的表观遗传密码的代谢破坏而发生的。我们最近发现,典型的肿瘤代谢物如何在不改变内源性干细胞维持基因的基线表达,但赋予细胞难以分化的表观遗传状态的情况下,显著提高产生CSC样状态的核重编程过程的整体动力学效率。这项研究强调,代谢-表观遗传通讯轴可以在癌症疾病的自然史中指导CSC的发育和维持。

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Nuclear reprogramming of cancer stem cells: Corrupting the epigenetic code of cell identity with oncometabolites.癌症干细胞的核重编程:用致癌代谢物破坏细胞身份的表观遗传密码。
Mol Cell Oncol. 2016 Mar 28;3(6):e1160854. doi: 10.1080/23723556.2016.1160854. eCollection 2016.
2
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Metabolic control of cancer cell stemness: Lessons from iPS cells.癌细胞干性的代谢调控:来自诱导多能干细胞的启示。
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Senescence-Inflammatory Regulation of Reparative Cellular Reprogramming in Aging and Cancer.衰老与癌症中修复性细胞重编程的衰老-炎症调节
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本文引用的文献

1
Oncometabolic Nuclear Reprogramming of Cancer Stemness.癌症干性的肿瘤代谢性核重编程
Stem Cell Reports. 2016 Mar 8;6(3):273-83. doi: 10.1016/j.stemcr.2015.12.012. Epub 2016 Feb 11.
2
Metabolic Reprogramming of Stem Cell Epigenetics.干细胞表观遗传学的代谢重编程
Cell Stem Cell. 2015 Dec 3;17(6):651-662. doi: 10.1016/j.stem.2015.11.012.
3
Metabostemness: Metaboloepigenetic reprogramming of cancer stem-cell functions.代谢干性:癌症干细胞功能的代谢表观遗传重编程。
Oncoscience. 2014 Dec 26;1(12):803-6. doi: 10.18632/oncoscience.113. eCollection 2014.
4
Intracellular α-ketoglutarate maintains the pluripotency of embryonic stem cells.细胞内的 α-酮戊二酸维持胚胎干细胞的多能性。
Nature. 2015 Feb 19;518(7539):413-6. doi: 10.1038/nature13981. Epub 2014 Dec 10.
5
Metabostemness: a new cancer hallmark.代谢干性:癌症新标志。
Front Oncol. 2014 Sep 29;4:262. doi: 10.3389/fonc.2014.00262. eCollection 2014.
6
Methionine metabolism regulates maintenance and differentiation of human pluripotent stem cells.蛋氨酸代谢调控人类多能干细胞的维持和分化。
Cell Metab. 2014 May 6;19(5):780-94. doi: 10.1016/j.cmet.2014.03.017. Epub 2014 Apr 17.
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Premature termination of reprogramming in vivo leads to cancer development through altered epigenetic regulation.体内重编程的过早终止会导致表观遗传调控改变而引发癌症。
Cell. 2014 Feb 13;156(4):663-77. doi: 10.1016/j.cell.2014.01.005.
8
Influence of threonine metabolism on S-adenosylmethionine and histone methylation.苏氨酸代谢对 S-腺苷甲硫氨酸和组蛋白甲基化的影响。
Science. 2013 Jan 11;339(6116):222-6. doi: 10.1126/science.1226603. Epub 2012 Nov 1.
9
Metabolic regulation of epigenetics.代谢调控表观遗传学。
Cell Metab. 2012 Jul 3;16(1):9-17. doi: 10.1016/j.cmet.2012.06.001.
10
Metabolic reprogramming: a cancer hallmark even warburg did not anticipate.代谢重编程:癌症的一个标志,甚至连沃伯格都没有预料到。
Cancer Cell. 2012 Mar 20;21(3):297-308. doi: 10.1016/j.ccr.2012.02.014.