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活化诱导胞苷脱氨酶(AID)mRNA的高表达与慢性淋巴细胞白血病患者未突变的IGVH基因状态及不良细胞遗传学异常相关。

High expression of activation-induced cytidine deaminase (AID) mRNA is associated with unmutated IGVH gene status and unfavourable cytogenetic aberrations in patients with chronic lymphocytic leukaemia.

作者信息

Heintel D, Kroemer E, Kienle D, Schwarzinger I, Gleiss A, Schwarzmeier J, Marculescu R, Le T, Mannhalter C, Gaiger A, Stilgenbauer S, Döhner H, Fonatsch C, Jäger U

机构信息

Department of Internal Medicine I, Division of Hematology and Hemostaseology, University of Vienna, Austria.

出版信息

Leukemia. 2004 Apr;18(4):756-62. doi: 10.1038/sj.leu.2403294.

Abstract

Activation-induced cytidine deaminase (AID) is essential for somatic hypermutation of B-cells. We investigated the expression of AID mRNA by real-time polymerase chain reaction (PCR) in peripheral blood mononuclear cells of 80 patients with B-CLL. AID expression was detected in 45 of 80 patients (56%) at various levels, but was undetectable in 35 patients (44%). AID PCR positivity was associated with unmutated IGV(H) gene status (22 of 25 patients; P=0.002) and unfavourable cytogenetics (18 of 23 patients with deletion in 11q or loss of p53; P=0.040). Using a threshold level of 0.01-fold expression compared to Ramos control cells, even more significant associations were observed (P=0.001 for IGVH; P=0.002 for cytogenetics). A correlation was observed between individual AID levels and the percentage of V(H) homology (R=0.41; P=0.001). AID positivity predicted unmutated IGV(H) status with an odds ratio of 8.31 (P=0.003) and poor risk cytogenetics with an odds ratio of 3.46 (P=0.032). Significance was retained after adjustment for Binet or Rai stages. AID mRNA levels were stable over time. These data suggest a potential role of AID as a prognostic marker in B-CLL.

摘要

活化诱导胞苷脱氨酶(AID)对于B细胞的体细胞高频突变至关重要。我们通过实时聚合酶链反应(PCR)研究了80例B细胞慢性淋巴细胞白血病(B-CLL)患者外周血单个核细胞中AID mRNA的表达。80例患者中有45例(56%)检测到不同水平的AID表达,但35例患者(44%)未检测到。AID PCR阳性与未突变的IGV(H)基因状态相关(25例患者中有22例;P=0.002)以及不良细胞遗传学相关(11q缺失或p53缺失的23例患者中有18例;P=0.040)。与Ramos对照细胞相比,使用0.01倍表达的阈值水平,观察到更显著的相关性(IGVH为P=0.001;细胞遗传学为P=0.002)。观察到个体AID水平与V(H)同源性百分比之间存在相关性(R=0.41;P=0.001)。AID阳性预测未突变的IGV(H)状态的优势比为8.31(P=0.003),不良风险细胞遗传学的优势比为3.46(P=0.032)。在调整Binet或Rai分期后仍具有显著性。AID mRNA水平随时间稳定。这些数据表明AID在B-CLL中作为预后标志物具有潜在作用。

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