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The dark side of activation-induced cytidine deaminase: relationship with leukemia and beyond.

作者信息

Kinoshita Kazuo, Nonaka Taichiro

机构信息

Evolutionary Medicine, Shiga Medical Center Research Institute, Moriyama.

出版信息

Int J Hematol. 2006 Apr;83(3):201-7. doi: 10.1532/IJH97.06011.

DOI:10.1532/IJH97.06011
PMID:16720548
Abstract

Activation-induced cytidine deaminase (AID) is a unique cellular enzyme that can trigger point mutations and chromosomal translocations, both of which potentially disturb normal cellular metabolism and affect cancer initiation and progression. The involvement of AID in the progression of leukemia has been suggested by multiple groups on the basis of observations of the statistical correlation between AID expression and a poor prognosis of B-cell chronic lymphocytic leukemia. The fact that ectopic expression of AID in mice results in tumors of the lung and T-lymphocytes suggests an oncogenic role for AID. The inducible nature of AID expression indicates that AID might be induced and cause oncogenic mutations, even in epithelial tissues, where AID expression is absent or very weak under normal conditions. If AID can be induced in epithelial cells by inflammatory signals, as from B-lymphocytes, it may be involved in various pathologic conditions, including inflammation-and infection-associated cancers, for which the molecular mechanism is largely unknown, despite the clinical significance of these diseases.

摘要

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本文引用的文献

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PKA-mediated phosphorylation regulates the function of activation-induced deaminase (AID) in B cells.蛋白激酶A介导的磷酸化作用调节B细胞中活化诱导胞嘧啶脱氨酶(AID)的功能。
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Immunoglobulin gene diversification.免疫球蛋白基因多样化
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4
A target selection of somatic hypermutations is regulated similarly between T and B cells upon activation-induced cytidine deaminase expression.在激活诱导的胞苷脱氨酶表达后,T细胞和B细胞之间体细胞超突变的靶点选择受到类似的调控。
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DNA cleavage in immunoglobulin somatic hypermutation depends on de novo protein synthesis but not on uracil DNA glycosylase.免疫球蛋白体细胞超突变中的DNA切割依赖于从头合成蛋白质,而非尿嘧啶DNA糖基化酶。
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AID is expressed in germinal center B-cell-like and activated B-cell-like diffuse large-cell lymphomas and is not correlated with intraclonal heterogeneity.活化诱导胞嘧啶脱氨酶(AID)在生发中心B细胞样和活化B细胞样弥漫大B细胞淋巴瘤中表达,且与克隆内异质性无关。
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