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Characteristics of CARMA1-BCL10-MALT1-A20-NF-κB expression in T cell-acute lymphocytic leukemia

机译:T细胞急性淋巴细胞白血病中CARMA1-BCL10-MALT1-A20-NF-κB表达的特征

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摘要

BackgroundKnowledge of the oncogenic signaling pathways of T-cell acute lymphoblastic leukemia (T-ALL) remains limited. Constitutive aberrant activation of the nuclear factor kappa B (NF-κB) signaling pathway has been detected in various lymphoid malignancies and plays a key role in the development of these carcinomas. The zinc finger-containing protein, A20, is a central regulator of multiple NF-κB-activating signaling cascades. A20 is frequently inactivated by deletions and/or mutations in several B-and T-cell lymphoma subtypes. However, few A20 mutations and polymorphisms have been reported in T-ALL. Thus, it is of interest to analyze the expression characteristics of A20 and its regulating factors, including upstream regulators and the CBM complex, which includes CARMA1, BCL10, and MALT1.
机译:背景技术对T细胞急性淋巴细胞白血病(T-ALL)的致癌信号通路的了解仍然有限。已经在各种淋巴恶性肿瘤中检测到核因子κB(NF-κB)信号传导途径的组成型异常激活,并且在这些癌症的发展中起关键作用。含锌指蛋白A20是多个NF-κB激活信号级联反应的中央调节剂。 A20常因几种B细胞和T细胞淋巴瘤亚型的缺失和/或突变而失活。但是,在T-ALL中几乎没有A20突变和多态性的报道。因此,分析A20及其调控因子的表达特性(包括上游调控因子和包括CARMA1,BCL10和MALT1的CBM复合体)很有意义。

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