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染色质重塑因子BRG1在急性髓细胞白血病中作用的研究进展 被引量:2

Research Progress on the Role of Chromatin Remodeling Factor BRG1 in Acute Myeloid Leukemia ——Review
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摘要 BRG1(Brahma-related gene 1,BRG1)是染色质重塑复合体SWI/SNF中的重要的ATP酶亚基,其在细胞周期调控、DNA修复以及肿瘤发展中发挥重要作用。不同于以往作为抑癌基因的证据,最新的研究结果发现在急性髓细胞白血病(Acute myeloid leukemia,AML)中BRG1对于白血病细胞的生长维持起重要作用,并且这种作用对于正常造血干细胞是非必需的。深入研究BRG1在急性髓细胞白血病中的作用及机制,将有助于开发非常有潜力的靶向治疗策略。本文就BRG1在AML白血病细胞及白血病干细胞中的作用及相关机制做一综述,为AML靶向治疗策略的研究提供参考。 BRG1( Brahma-related gene 1,BRG1) is the ATPase subunit of SWI / SNF chromatin remodeling complexes,w hich plays an important role in cell cycle regulation,DNA repair and tumor development. Unlike the evidence as tumor suppressor genes in the past reports,latest researches show that BRG1 plays an important role in sustaining the grow th of leukemia cells in acute myeloid leukemia,and these effects on normal hematopoietic stem cells are dispensable. Further studies of the role and mechanism of BRG1 in acute myeloid leukemia w ill contribute to the development of a new and promising targeted therapy strategy. This article review s the role of BRG1 on leukemia cells and leukemia stem cells in AM L and discusses the related mechanism,w hich providing some reference for the targeted treatment strategy of AM L.
出处 《中国实验血液学杂志》 CAS CSCD 北大核心 2016年第3期930-933,共4页 Journal of Experimental Hematology
基金 南京市医学科技发展资金资助项目(QYK11163) 中央高校基本科研业务费专项资金资助(20620140662)
关键词 BRG1 急性髓细胞白血病 白血病干细胞 靶向治疗 BRG1 acute myeloid leukemia leukemia stem cell targeted therapy
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  • 1Polo SE, Kaidi A, Baskcomb L, Galanty Y, Jackson SP. Regulation of DNA-damage responses and cellcycle progression by the chromatin remodelling factor CHD4. EMBO J 2010; 29:3130-3139.
  • 2Larsen DH, Poinsignon C, Gudjonsson T, et al. The chromatin-remodeling factor CHD4 coordinates signaling and repair after DNA damage. J Cell Biol 190:731-740.
  • 3Smeenk G, Wiegant WW, Vrolijk H, et al. The NuRD chromatin-remodeling complex regulates signaling and repair of DNA damage. J Cell Biol 190:741-749.
  • 4Luo J, Su F, Chen D, Shiloh A, Gu W. Deacetylation of p53 modulates its effect on cell growth and apoptosis. Nature 2000; 408:377-381.
  • 5Pegoraro G, Kubben N, Wickert U, et al. Ageing-related chromatin defects through loss of the NURD complex. Nat Cell Biol 2009; 11:1261-1267.
  • 6Bagchi A, Papazoglu C, Wu Y, et al. CHD5 is a tumor suppressor at human lp36. Cell 2007; 128:459-475.
  • 7Hurd EA, Poucher HK, Cheng K, Raphael Y, Martin DM. The ATP-dependent chromatin remodeling enzyme CHD7 regulates pro-neural gene expression and neurogenesis in the inner ear. Development 2010; 137:3139-3150.
  • 8Bosman EA, Penn AC, Ambrose JC, et al. Multiple mutations in mouse Chd7 provide models for CHARGE syn- drome. Hum Mol Genet 2005; 14:3463-3476.
  • 9Schnetz MP, Handoko L, Akhtar-Zaidi B, et al. CHD7 targets active gene enhancer elements to modulate ES cell-specific gene expression. PLoS Genet 6:e 1001023.
  • 10Hurd EA, Capers PL, Blauwkamp MN, et al. Loss of Chd7 function in gene-trapped reporter mice is embryonic lethal and associated with severe defects in multiple developing tissues. Mamm Genome 2007: 18:94-104.

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