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Strong expression of EZH2 and accumulation of trimethylated H3K27 in diffuse large B-cell lymphoma independent of cell of origin and EZH2 codon 641 mutation

机译:EZH2的强表达和三甲基化H3K27在弥漫性大B细胞淋巴瘤中的表达,与原发细胞和EZH2密码子641突变无关

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摘要

Gain-of-function EZH2 mutation promotes H3K27 trimethylation (H3K27me3) and lymphoid transformation of germinal center (GC) derived B-cell lymphoma, such as GCB diffuse large B-cell lymphoma (DLBCL), but not activated B-cell (ABC) DLBCL. It is unclear whether expression levels of EZH2 and consequential H3K27me3 vary by EZH2 mutation and/or cell-of-origin in DLBCL. Ninety lymphoma samples including 40 DLBCLs were studied by immunohistochemistry. EZH2 Y641 mutations were detected in three of 20 (15%) GCB and none of 20 ABC types. All 40 DLBCLs showed strong EZH2, expression with high-level H3K27me3 in 90% GCBs and 95% ABCs. In 50 other B-cell lymphomas except for follicular lymphoma, strong EZH2 expression correlated with high-grade features. Immunoblot of DLBCL cell lines and microarray gene expression study of EZH2 in B-cell lymphomas were consistent with the immunohistochemistry findings. High-level EZH2 and H3K27me3 were common in DLBCL independent of cell-of-origin and EZH2 mutation. High-level EZH2 in lymphoma of aggressive features suggests additional therapeutic targets.
机译:功能获得性EZH2突变促进H3K27三甲基化(H3K27me3)和生发中心(GC)衍生的B细胞淋巴瘤(如GCB弥漫性大B细胞淋巴瘤(DLBCL),但未激活的B细胞(ABC)的淋巴样转化DLBCL。尚不清楚EZH2和相应的H3K27me3的表达水平是否因EZH2突变和/或DLBCL中的起源细胞而异。通过免疫组织化学研究了包括40个DLBCLs在内的90个淋巴瘤样本。在20种GCB中的3种(15%)中检测到EZH2 Y641突变,在20种ABC类型中均未检测到。所有40个DLBCLs均显示强EZH2,在90%的GCB和95%的ABC中均以高水平的H3K27me3表达。除滤泡性淋巴瘤外,在其他50例B细胞淋巴瘤中,强EZH2表达与高级别特征相关。 B细胞淋巴瘤中DLBCL细胞系的免疫印迹和EZH2基因芯片基因表达的研究与免疫组化结果一致。高水平的EZH2和H3K27me3在DLBCL中很常见,与起源细胞和EZH2突变无关。侵略性淋巴瘤中高水平的EZH2提示了其他治疗靶点。

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