首页> 美国卫生研究院文献>Cancer Science >MUM1/IRF4 Expression Is an Unfavorable Prognostic Factor in B‐Cell Chronic Lymphocytic Leukemia (CLL)/Small Lymphocytic Lymphoma (SLL)
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MUM1/IRF4 Expression Is an Unfavorable Prognostic Factor in B‐Cell Chronic Lymphocytic Leukemia (CLL)/Small Lymphocytic Lymphoma (SLL)

机译:MUM1 / IRF4表达是B细胞慢性淋巴细胞性白血病(CLL)/小淋巴细胞性淋巴瘤(SLL)的不利预后因素

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摘要

B‐Cell chronic lymphocytic leukemia (B‐CLL)/small lymphocytic lymphoma (SLL) consists of heterogeneous diseases that are distinguished by morphological, immunophenotypic and molecular features. MUM1 (multiple myeloma oncogene 1) is a protooncogene that is deregulated as a result of (6;14)(p25;q32) chromosomal translocation in multiple myeloma, and is also expressed in a variety of malignant lymphoma entities. We examined the expression of MUM1 in B‐CLL/SLL, and found that 2 of 4 B‐CLL‐derived cell lines and 14 of 29 patients' specimens expressed MUM1 by immunohistochemical analysis. MUM1 expression was not associated with CD38 expression, somatic hypermutation of immunoglobulin heavy chain gene variable region (IgVH), or any other clinical characteristics of the patients. Interestingly, the patients who were positive for MUM1 showed shorter overall survival tunes than those who were negative for MUM1 (50% survival: 22 months vs. 82 months) (P=0.0008, log‐rank test). Multivariate analysis by Cox's proportional‐hazards regression model showed that MUM1 expression and unmutated IgVH status were independent unfavorable prognostic factors in patients with B‐CLL/SLL. These findings suggest that MUM1 expression is a useful prognostic factor in B‐CLL/SLL. The biological role and mechanism of action of MUM1 in B‐CLL/SLL need to be clarified for the development of therapies for patients with the poor prognostic subtype.
机译:B细胞慢性淋巴细胞性白血病(B‐CLL)/小淋巴细胞性淋巴瘤(SLL)由异质性疾病组成,这些异质性疾病的特征在于形态,免疫表型和分子特征。 MUM1(多发性骨髓瘤癌基因1)是一种原癌基因,由于多发性骨髓瘤中的(6; 14)(p25; q32)染色体易位而被失调,并且还在多种恶性淋巴瘤实体中表达。我们检查了MUM1在B‐CLL / SLL中的表达,并通过免疫组织化学分析发现4个B‐CLL衍生的细胞系中有2个和29个患者的标本中有14个表达了MUM1。 MUM1表达与CD38表达,免疫球蛋白重链基因可变区(IgVH)的体细胞超突变或患者的任何其他临床特征无关。有趣的是,MUM1阳性的患者的总体生存期短于MUM1阴性的患者(50%生存期:22个月vs. 82个月)(P = 0.0008,对数检验)。 Cox比例风险回归模型的多变量分析表明,MUM1表达和未突变的IgVH状态是B‐CLL / SLL患者的独立不良预后因素。这些发现表明MUM1表达是B‐CLL / SLL中有用的预后因素。需要明确MUM1在B‐CLL / SLL中的生物学作用和作用机制,以开发针对预后差的亚型患者的疗法。

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