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多发性骨髓瘤癌基因1(MUM1)/干扰素调节因子4(IRF4)上调B细胞恶性肿瘤中γ干扰素诱导的单核因子(MIG)基因表达。

Multiple myeloma oncogene 1 (MUM1)/interferon regulatory factor 4 (IRF4) upregulates monokine induced by interferon-gamma (MIG) gene expression in B-cell malignancy.

作者信息

Uranishi M, Iida S, Sanda T, Ishida T, Tajima E, Ito M, Komatsu H, Inagaki H, Ueda R

机构信息

Department of Internal Medicine and Molecular Science, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.

出版信息

Leukemia. 2005 Aug;19(8):1471-8. doi: 10.1038/sj.leu.2403833.

Abstract

MUM1 (multiple myeloma oncogene 1)/IRF4 (interferon regulatory factor 4) is a transcription factor that is activated as a result of t(6;14)(p25;q32) in multiple myeloma. MUM1 expression is seen in various B-cell lymphomas and predicts an unfavorable outcome in some lymphoma subtypes. To elucidate its role in B-cell malignancies, we prepared MUM1-expressing Ba/F3 cells, which proliferated until higher cellular density than the parental cells, and performed cDNA microarray analysis to identify genes whose expression is regulated by MUM1. We found that the expression of four genes including FK506-binding protein 3 (FKBP3), the monokine induced by interferon-gamma(MIG), Fas apoptotic inhibitory molecule (Faim) and Zinc-finger protein 94 was altered in the MUM1-expressing cells. We then focused on MIG since its expression was immediately upregulated by MUM1. In reporter assays, MUM1 activated the MIG promoter in cooperation with PU.1, and the interaction between MUM1 and the MIG promoter sequence was confirmed. The expression of MIG was correlated with that of MUM1 in B-CLL cell lines, and treatment with neutralizing antibodies against MIG and its receptor, CXCR3, slightly inhibited the proliferation of two MUM1-expressing lines. These results suggest that MUM1 plays roles in the progression of B-cell lymphoma/leukemia by regulating the expression of various genes including MIG. Leukemia (2005) 19, 1471-1478. doi:10.1038/sj.leu.2403833; published online 16 June 2005.

摘要

多发性骨髓瘤癌基因1(MUM1)/干扰素调节因子4(IRF4)是一种转录因子,在多发性骨髓瘤中因t(6;14)(p25;q32)而被激活。MUM1表达见于多种B细胞淋巴瘤,并预示某些淋巴瘤亚型的预后不良。为阐明其在B细胞恶性肿瘤中的作用,我们制备了表达MUM1的Ba/F3细胞,其增殖至比亲代细胞更高的细胞密度,并进行cDNA微阵列分析以鉴定其表达受MUM1调控的基因。我们发现,在表达MUM1的细胞中,包括FK506结合蛋白3(FKBP3)、干扰素-γ诱导的单核因子(MIG)、Fas凋亡抑制分子(Faim)和锌指蛋白94在内的四个基因的表达发生了改变。然后我们聚焦于MIG,因为其表达被MUM1立即上调。在报告基因分析中,MUM1与PU.1协同激活MIG启动子,并证实了MUM1与MIG启动子序列之间的相互作用。在B-CLL细胞系中,MIG的表达与MUM1的表达相关,用抗MIG及其受体CXCR3的中和抗体处理可轻微抑制两个表达MUM1的细胞系的增殖。这些结果表明,MUM1通过调节包括MIG在内的多种基因的表达在B细胞淋巴瘤/白血病的进展中发挥作用。《白血病》(2005年)19卷,1471 - 1478页。doi:10.1038/sj.leu.2403833;2005年6月16日在线发表。

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