Optimal Use of Biomarkers in Oncology: Expression of Activation-induced Cytidine Deaminase (AID/AICDA) in Follicular Lymphoma

Y. Yakushijin
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Abstract

Follicular lymphoma (FL), which originates in germinal center B-lymphocytes, has been recognized to be a heterogeneous entity in some patients developing progressive or transformed diseases. Secondary genetic events after t(14;18) translocation have been associated with this histological transformation, such as c-myc amplification and/or translocation. Activation-induced cytidine deaminase (AID/AICDA) is required for somatic hyper-mutation and class switch recombination of immunoglobulin genes, and c-myc translocation of the germinal centre derived B-cell lymphoma. The role of AID in FL pathogenesis has not been established. Here we tried to identify the significance of AID associated with c-myc in the progression of FL, and showed that switched-off AID or a low expression of AID after c-myc amplification might correlate to rapidly progressive FL as well as to overall clinical outcomes.
肿瘤生物标志物的最佳使用:激活诱导胞苷脱氨酶(AID/AICDA)在滤泡性淋巴瘤中的表达
滤泡性淋巴瘤(FL)起源于生发中心b淋巴细胞,已被认为是一些发展为进行性或转化性疾病的患者的异质性实体。t(14;18)易位后的继发性遗传事件与这种组织学转变有关,如c-myc扩增和/或易位。激活诱导胞苷脱氨酶(AID/AICDA)是免疫球蛋白基因的体细胞超突变和类开关重组以及生发中心源性b细胞淋巴瘤的c-myc易位所必需的。AID在FL发病机制中的作用尚未确定。在这里,我们试图确定AID与c-myc在FL进展中的重要性,并表明在c-myc扩增后AID的关闭或低表达可能与快速进展的FL以及总体临床结果相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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