期刊文献+

microRNA--新的髓系白血病致病因子及临床标志物 被引量:1

MicroRNAs:New Pathogenic Factors and Clinical Markers in Myeloid Leukemia
下载PDF
导出
摘要 微RNA(MicroRNA,miRNA)是一类长18~25 nt的非编码RNA,主要通过与靶基因mRNA3′UTR上的互补区域结合后在转录后水平(RNA切割或翻译抑制)负性调控靶基因的表达.现已发现,miRNA参与了多种正常细胞过程以及肿瘤发生的调控.miRNA也在造血链系分化和相关白血病中发挥重要作用.急性髓系白血病(AML)是一种涉及多种遗传学变异的造血恶性肿瘤,在中国的髓系白血病中发病率最高.在不同遗传学特征的AML中,miRNAs具有差异表达谱,这种差异表达谱可作为AML临床诊断和预后的依据.一些在白血病中表达异常的miRNAs的致癌作用机制已被阐明,今后有望开发针对这些miRNAs的药物,从而为白血病的治疗提供新的靶点. MicroRNAs(miRNAs) are a family of small non-coding RNAs of 18 ~ 25 nucleotides that interact with the 3′ UTR of targeted native coding mRNAs to reduce their cleavage or translation repression,thus to negatively regulate the expression of target genes at the post-transcriptional level.It had been demonstrated that miRNAs were extensively involved in many cell activity and cancer pathogenesis,including several aspects that play an important functions in the differentiation of hematopoietic lineage and related to leukemia.Acute myeloid leukemia(AML) is a heterogeneous type of genetically diverse hematopoietic malignancies with the highest morbidity in China among all types of myeloid leukemia.Aberrant microRNAs expression were observed in various genetic subtypes of AMLs,and could be used as markers for leukemia diagnosis or prognosis.The function of certain microRNAs in normal lineage development has been explored,meanwhile the abnormally expressed microRNAs in myeloid leukemia have been shown to functionally relevant to leukemogenesis.Hence,developing targeting medicine of specific miRNAs is promising as a novel approach for myeloid leukemia therapy.
出处 《中国生物化学与分子生物学报》 CAS CSCD 北大核心 2011年第4期293-299,共7页 Chinese Journal of Biochemistry and Molecular Biology
基金 国家自然科学基金资助项目(No.30970616)~~
关键词 微RNA 髓系白血病 预后和治疗 microRNA myeloid leukemia prognosis and therapy
  • 相关文献

参考文献42

  • 1Vasudevan S, Tong Y, Steitz J A. Switching from repression to activation : microRNAs can up-regulate translation [ J ]. Science, 2007,318 (5858) : 1931-1934.
  • 2Gfiffiths-Jones S, Saini H K, van Dongen S, et al. miRBase: tools for microRNA genomics [ J ]. Nucleic Acids Res, 2008,36 ( Database Issue) : D154-D158.
  • 3Tenen D G. Disruption of differentiation in human cancer: AML shows the wav [J].Nat Rev Cancer.2003.3 (2) :89-101.
  • 4Estey E, Dohner H. Acute myeloid leukaemia[ J]. Lancet,2006, 368(9550) : 1894-1907.
  • 5Lane S W, Scadden D T, Gilliland D G. The leukemic stem cell niche: current concepts and therapeutic opportunities[ J]. Blood, 2009,114 (6) : 1150-1157.
  • 6Isken F, Steffen B, Merk S,et al. Identification of acute myeloid leukaemia associated microRNA expression patterns [ J ]. Br J Haematol,2008,140 ( 2 ) : 153-161.
  • 7Garzon R, Heaphy C E, Havelange V, et al. MicroRNA 29b functions in acute myeloid leukemia [ J ]. Blood,2009,114 ( 26 ) : 5331-5341.
  • 8Woods K, Thomson J M, Hammond S M. Direct regulation of an oncogenic micro-RNA cluster by E2F transcription factors [ J]. J Biol Chem,2007,282(4) : 2130-2134.
  • 9Takamizawa J, Konishi H, Yanagisawa K, et al. Reduced expression of the let-7 microRNAs in human lung cancers in association with shortened postoperative survival[ J ]. Cancer Res, 2004,64( 11 ) :3753-3756.
  • 10Garzon R, Volinia S, Liu C G, et al. MicroRNA signatures associated with cytogenetics and prognosis in acute myeloid leukaemia[J]. Blood ,2008,111 (6) :3183-3189.

同被引文献2

引证文献1

二级引证文献4

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部