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BCL-6抑制在淋巴细胞分化、炎症和细胞周期控制中起作用的基因。

BCL-6 represses genes that function in lymphocyte differentiation, inflammation, and cell cycle control.

作者信息

Shaffer A L, Yu X, He Y, Boldrick J, Chan E P, Staudt L M

机构信息

Metabolism Branch, Division of Clinical Sciences, National Cancer Institute, Bethesda, Maryland 20892, USA.

出版信息

Immunity. 2000 Aug;13(2):199-212. doi: 10.1016/s1074-7613(00)00020-0.

Abstract

BCL-6, a transcriptional repressor frequently translocated in lymphomas, regulates germinal center B cell differentiation and inflammation. DNA microarray screening identified genes repressed by BCL-6, including many lymphocyte activation genes, suggesting that BCL-6 modulates B cell receptor signals. BCL-6 repression of two chemokine genes, MIP-1alpha and IP-10, may also attenuate inflammatory responses. Blimp-1, another BCL-6 target, is important for plasmacytic differentiation. Since BCL-6 expression is silenced in plasma cells, repression of blimp-1 by BCL-6 may control plasmacytic differentiation. Indeed, inhibition of BCL-6 function initiated changes indicative of plasmacytic differentiation, including decreased expression of c-Myc and increased expression of the cell cycle inhibitor p27kip1. These data suggest that malignant transformation by BCL-6 involves inhibition of differentiation and enhanced proliferation.

摘要

BCL-6是一种在淋巴瘤中频繁易位的转录抑制因子,可调节生发中心B细胞分化和炎症反应。DNA微阵列筛选鉴定出受BCL-6抑制的基因,包括许多淋巴细胞激活基因,这表明BCL-6可调节B细胞受体信号。BCL-6对两种趋化因子基因MIP-1α和IP-10的抑制作用,也可能减弱炎症反应。Blimp-1是BCL-6的另一个靶点,对浆细胞分化很重要。由于BCL-6在浆细胞中表达沉默,BCL-6对blimp-1的抑制作用可能控制浆细胞分化。事实上,抑制BCL-6功能引发了指示浆细胞分化的变化,包括c-Myc表达降低和细胞周期抑制剂p27kip1表达增加。这些数据表明,BCL-6介导的恶性转化涉及分化抑制和增殖增强。

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