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MEK1 signaling promotes self-renewal and tumorigenicity of liver cancer stem cells via maintaining SIRT1 protein stabilization.MEK1信号传导通过维持SIRT1蛋白稳定性促进肝癌干细胞的自我更新和致瘤性。
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本文引用的文献

1
Resveratrol ameliorates ionizing irradiation-induced long-term hematopoietic stem cell injury in mice.白藜芦醇可改善电离辐射诱导的小鼠长期造血干细胞损伤。
Free Radic Biol Med. 2013 Jan;54:40-50. doi: 10.1016/j.freeradbiomed.2012.10.530. Epub 2012 Nov 1.
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Selective elimination of leukemia stem cells: hitting a moving target.选择性清除白血病干细胞:击中移动的目标。
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Accelerating cancer evolution: a dark side of SIRT1 in genome maintenance.加速癌症演变:SIRT1在基因组维持中的阴暗面
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Cancer stem cells: impact, heterogeneity, and uncertainty.癌症干细胞:影响、异质性和不确定性。
Cancer Cell. 2012 Mar 20;21(3):283-96. doi: 10.1016/j.ccr.2012.03.003.
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SIRT1 deacetylase promotes acquisition of genetic mutations for drug resistance in CML cells.SIRT1 去乙酰化酶促进 CML 细胞获得耐药性的基因突变。
Oncogene. 2013 Jan 31;32(5):589-98. doi: 10.1038/onc.2012.83. Epub 2012 Mar 12.
6
Activation of p53 by SIRT1 inhibition enhances elimination of CML leukemia stem cells in combination with imatinib.SIRT1 抑制激活 p53 增强伊马替尼联合消除 CML 白血病干细胞的作用。
Cancer Cell. 2012 Feb 14;21(2):266-81. doi: 10.1016/j.ccr.2011.12.020.
7
aSIRTing control over cancer stem cells.靶向 SIRT 治疗以控制肿瘤干细胞。
Cancer Cell. 2012 Feb 14;21(2):140-2. doi: 10.1016/j.ccr.2012.01.014.
8
NAD-dependent histone deacetylase, SIRT1, plays essential roles in the maintenance of hematopoietic stem cells.NAD 依赖性组蛋白去乙酰化酶 SIRT1 在维持造血干细胞中发挥重要作用。
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9
Aging, rejuvenation, and epigenetic reprogramming: resetting the aging clock.衰老、返老还童和表观遗传重编程:重置衰老时钟。
Cell. 2012 Jan 20;148(1-2):46-57. doi: 10.1016/j.cell.2012.01.003.
10
SIRT1 is dispensable for function of hematopoietic stem cells in adult mice.SIRT1 对于成年小鼠造血干细胞的功能并非不可或缺。
Blood. 2012 Feb 23;119(8):1856-60. doi: 10.1182/blood-2011-09-377077. Epub 2012 Jan 4.

沉默调节蛋白、组织维持与肿瘤发生

Sirtuins, tissue maintenance, and tumorigenesis.

作者信息

Mohrin Mary, Chen Danica

机构信息

University of California, Berkeley, CA, USA.

出版信息

Genes Cancer. 2013 Mar;4(3-4):76-81. doi: 10.1177/1947601912474930.

DOI:10.1177/1947601912474930
PMID:24019997
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3764468/
Abstract

Aging is a degenerative process resulting in compromised tissue maintenance and increased susceptibility to diseases, such as cancer. Recent advancements support the notion that aging is a highly regulated process governed by evolutionarily conserved pathways. In mammals, tissue-specific adult stem cells (ASCs) persist throughout the lifetime to maintain and repair tissues. While reduced ASC self-renewal is thought to contribute to compromised tissue maintenance, increased self-renewal of cancer stem cells (CSCs) may lead to tumorigenesis. It is speculated that genetic regulators of aging, such as sirtuins, are likely to impinge upon the ASC compartments to regulate tissue maintenance and tumorigenesis. In this review, we discuss the emerging evidence linking sirtuins to normal and malignant ASC self-renewal, tissue maintenance, and tumorigenesis.

摘要

衰老乃一退行性过程,会导致组织维持功能受损,并增加对诸如癌症等疾病的易感性。近期进展支持这样一种观点,即衰老乃是一个由进化上保守的通路所调控的高度有序的过程。在哺乳动物中,组织特异性成体干细胞(ASC)终生存在以维持和修复组织。虽然ASC自我更新能力的降低被认为会导致组织维持功能受损,但癌症干细胞(CSC)自我更新能力的增强可能会导致肿瘤发生。据推测,衰老的遗传调节因子,如沉默调节蛋白,可能会影响ASC区室以调节组织维持和肿瘤发生。在本综述中,我们讨论了将沉默调节蛋白与正常和恶性ASC自我更新、组织维持及肿瘤发生联系起来的新证据。