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Targeting Sirt-1 controls GVHD by inhibiting T-cell allo-response and promoting Treg stability in mice.靶向 Sirt-1 通过抑制 T 细胞同种反应和促进 Treg 稳定性来控制 GVHD。
Blood. 2019 Jan 17;133(3):266-279. doi: 10.1182/blood-2018-07-863233. Epub 2018 Dec 4.
2
SIRT1 rs3758391 polymorphism and risk of diffuse large B cell lymphoma in a Chinese population.SIRT1基因rs3758391多态性与中国人群弥漫性大B细胞淋巴瘤风险
Cancer Cell Int. 2018 Oct 22;18:163. doi: 10.1186/s12935-018-0659-z. eCollection 2018.
3
SIRT1 Activation Disrupts Maintenance of Myelodysplastic Syndrome Stem and Progenitor Cells by Restoring TET2 Function.SIRT1 激活通过恢复 TET2 功能破坏骨髓增生异常综合征干细胞和祖细胞的维持。
Cell Stem Cell. 2018 Sep 6;23(3):355-369.e9. doi: 10.1016/j.stem.2018.07.018. Epub 2018 Aug 23.
4
The IRF9-SIRT1-P53 axis is involved in the growth of human acute myeloid leukemia.IRF9-SIRT1-P53 轴参与了人类急性髓系白血病的生长。
Exp Cell Res. 2018 Apr 15;365(2):185-193. doi: 10.1016/j.yexcr.2018.02.036. Epub 2018 Mar 6.
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How I manage relapse of chronic myeloid leukaemia after stopping tyrosine kinase inhibitor therapy.酪氨酸激酶抑制剂治疗停药后,我如何处理慢性髓性白血病复发问题。
Br J Haematol. 2018 Jan;180(1):24-32. doi: 10.1111/bjh.14973. Epub 2017 Oct 19.
6
SIRT1 and AMPK pathways are essential for the proliferation and survival of primary effusion lymphoma cells.沉默信息调节因子1(SIRT1)和腺苷酸活化蛋白激酶(AMPK)信号通路对于原发性渗出性淋巴瘤细胞的增殖和存活至关重要。
J Pathol. 2017 Jul;242(3):309-321. doi: 10.1002/path.4905. Epub 2017 May 13.
7
Tenovin-6 inhibits proliferation and survival of diffuse large B-cell lymphoma cells by blocking autophagy.Tenovin-6通过阻断自噬来抑制弥漫性大B细胞淋巴瘤细胞的增殖和存活。
Oncotarget. 2017 Feb 28;8(9):14912-14924. doi: 10.18632/oncotarget.14741.
8
A 17-gene stemness score for rapid determination of risk in acute leukaemia.一种用于快速确定急性白血病风险的 17 基因干性评分。
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9
The genetics of myelodysplastic syndrome: from clonal haematopoiesis to secondary leukaemia.骨髓增生异常综合征的遗传学:从克隆性造血到继发性白血病
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10
SIRT1 and LSD1 competitively regulate KU70 functions in DNA repair and mutation acquisition in cancer cells.SIRT1和LSD1在癌细胞的DNA修复和突变获得过程中竞争性调节KU70的功能。
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SIRT1 在血液系统恶性肿瘤中的作用。

Role of SIRT1 in hematologic malignancies.

机构信息

Department of Hematological Malignancies Translational Science, Gehr Family Center for Leukemia Research, Hematologic Malignancies and Stem Cell Transplantation Institute, Beckman Research Institute, City of Hope Medical Center, Duarte, CA 91010, USA.

Department of Hematology, Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University, Hangzhou 310016, China.

出版信息

J Zhejiang Univ Sci B. 2019 May;20(5):391-398. doi: 10.1631/jzus.B1900148.

DOI:10.1631/jzus.B1900148
PMID:31090265
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6568226/
Abstract

Sirtuin 1 (SIRT1) is a protein deacetylase, which regulates various physiological activities by deacetylating different protein substrates. An increasing number of studies have revealed critical roles of SIRT1 in different aspects of cancers including metabolism, proliferation, genomic instability, and chemotherapy resistance. Depending on the protein targets in a certain oncogenic context, SIRT1 may play a unique role in each individual blood cancer subtype. Our previous work showed that activation of SIRT1 in primitive leukemia cells of acute myeloid leukemia (AML) and chronic myelogenous leukemia (CML) promotes disease maintenance. On the other hand, an SIRT1 agonist was shown to disrupt maintenance of myelodysplastic syndrome (MDS) stem cells and holds promise as a potential therapeutic approach. Herein, we present a concise summary of the different functions of SIRT1 in hematologic malignancies.

摘要

Sirtuin 1(SIRT1)是一种蛋白去乙酰化酶,通过去乙酰化不同的蛋白底物来调节各种生理活动。越来越多的研究揭示了 SIRT1 在癌症的不同方面的关键作用,包括代谢、增殖、基因组不稳定性和化疗耐药性。根据特定致癌环境中的蛋白靶点,SIRT1 在每种个体血液癌亚型中可能发挥独特的作用。我们之前的工作表明,急性髓系白血病(AML)和慢性髓系白血病(CML)原始白血病细胞中 SIRT1 的激活促进了疾病的维持。另一方面,SIRT1 激动剂被证明可以破坏骨髓增生异常综合征(MDS)干细胞的维持,并有望成为一种潜在的治疗方法。本文简要总结了 SIRT1 在血液恶性肿瘤中的不同功能。