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首页> 外文期刊>Immunological Investigations: A Journal of Molecular and Cellular Immunology >Investigation of AID, Dicer, and Drosha Expressions in Patients with Chronic Lymphocytic Leukemia
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Investigation of AID, Dicer, and Drosha Expressions in Patients with Chronic Lymphocytic Leukemia

机译:慢性淋巴细胞白血病患者的辅助,DICER和DROSHA表达调查

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Chronic lymphocytic leukemia (CLL) is the most common leukemia in Western countries. Cytogenetic lesions such as del13q14, del11q22.3, and del17p13 are identified in 5060% of patients. Activation-induced cytidine deaminase (AID) plays a central role in somatic hyper mutation (SHM) and class switch recombination (CSR) and functions on Ig genes, but also target non-Ig genes, and over-expression of AID can lead to point mutations or translocations in non-Ig genes such as IgH/Myc translocation. Dicer and Drosha, which have a role in activation process of miRNA, also act in a double-strand DNA break (DSB) repair mechanism. In this study, whether the changes of AID, Dicer and Drosha expressions may be associated with both deletions and clinical outcomes in patients with CLL were investigated. AID expressions were increased in patients with CLL. However, cell lysate AID protein levels were only increased in patients with del17p or del11q who have poor prognosis. Decreased Dicer expressions were found in patients with deletion, whereas increased Drosha expressions were found in patients without deletion and with del13q. According to Rai and Binet staging systems, advanced-stage patients showed increased AID protein levels, decreased Dicer and Drosha expressions. Our findings may suggest that high AID expression and lower Dicer expression were observed in patients with CLL especially del17p and del11q and might associated with deletions such as del17p and del11q. AID, Dicer, and Drosha expressions might be used as an indicator of prognosis for CLL. ?2017 Taylor & Francis.
机译:慢性淋巴细胞白血病(CLL)是西方国家最常见的白血病。在5060%的患者中确定了诸如Del13Q14,Del11q22.3和Del17P13的细胞遗传学病变。活化诱导的胞苷脱氨酶(AID)在体细胞异常突变(SHM)和阶级开关重组(CSR)中起着核心作用,并且在IG基因上的作用,但也靶向非IG基因,并且助剂的过表达可能导致点非Ig基因中的突变或易位,例如IGH / MYC易位。 Dicer和Drosha在miRNA的激活过程中具有作用,也以双链DNA断裂(DSB)修复机制起作用。在该研究中,是否可以对CLL患者进行缺失和临床结果有关辅助,DICER和DROSHA表达的变化。 CLL患者的帮助表达增加。然而,在Del17P或Del11Q的患者患者患者患者患者患者患者缺乏预后差。在缺失患者中发现了减少的Dicer表达,而没有删除和Del13Q的患者发现增加的Drosha表达。根据RAI和BINET分期系统,先进阶段的患者显示援助蛋白水平增加,DICER和DROSHA表达增加。我们的发现可能表明,CLL特别是DEL17P和DEL11Q的患者中观察到高助剂表达和降低的DICER表达,并且可能与DEL17P和DEL11Q等缺失相关。 AID,DICER和DROSHA表达可以用作CLL预后的指标。 ?2017泰勒&弗朗西斯。

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