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EZH2 的表达依赖于弥漫性大 B 细胞淋巴瘤中 MYC 和 TP53 的调控。

EZH2 expression is dependent on MYC and TP53 regulation in diffuse large B-cell lymphoma.

机构信息

LABGEM, Departamento de Patologia e Medicina Legal, Universidade Federal Do Ceará, Fortaleza, Brazil.

Serviço de Patologia, Instituto do Câncer do Ceará, Fortaleza, Brazil.

出版信息

APMIS. 2020 Apr;128(4):308-315. doi: 10.1111/apm.13029. Epub 2020 Feb 27.

Abstract

EZH2 is an important epigenetic regulator, but its role in diffuse large B-cell lymphoma (DLBCL) pathogenesis and its relationship with MYC, BCL2, and TP53 expression, chromosomal rearrangements, and clinical features are still poorly understood. So, we investigated EZH2 expression and its associations with the immunophenotypic presentations, including MYC, BCL2, and TP53 expression, MYC, BCL2, and BCL6 translocation status, clinicopathological features, and therapeutic response to R-CHOP in a series of 139 DLBCL cases. EZH2 positivity was associated with MYC and TP53 expression (p = 0.0002 and p = 0.0000, respectively) and to high proliferative index (Ki67>70%, p = 0.0082). No associations were found among EZH2 expression and chromosomal translocation status. The non-germinal center (nGC) DLBCL presented most of associations observed in the general sample; however, only TP53 immunodetection showed associations with EZH2 expression in the germinal center (GC) DLBCL. EZH2 expression had no impact on therapeutic efficacy in R-CHOP-treated patients. In conclusion, EZH2 seems to be upregulated by MYC, to rely on TP53 alterations, and is associated with high proliferative tumors in DLBCL, which might be dependent on GC or nGC subclassifications. Furthermore, it is not a therapeutic efficacy marker to R-CHOP in our series.

摘要

EZH2 是一种重要的表观遗传调节剂,但它在弥漫性大 B 细胞淋巴瘤(DLBCL)发病机制中的作用及其与 MYC、BCL2 和 TP53 表达、染色体重排和临床特征的关系仍知之甚少。因此,我们研究了 EZH2 的表达及其与免疫表型的关系,包括 MYC、BCL2 和 TP53 表达、MYC、BCL2 和 BCL6 易位状态、临床病理特征以及对 R-CHOP 的治疗反应在一系列 139 例 DLBCL 病例中。EZH2 阳性与 MYC 和 TP53 表达相关(p=0.0002 和 p=0.0000)和高增殖指数(Ki67>70%,p=0.0082)相关。EZH2 表达与染色体易位状态之间没有关联。非生发中心(nGC)DLBCL 表现出与一般样本中观察到的大多数关联;然而,只有生发中心(GC)DLBCL 中的 TP53 免疫检测与 EZH2 表达相关。EZH2 表达对 R-CHOP 治疗患者的疗效没有影响。总之,EZH2 似乎被 MYC 上调,依赖于 TP53 改变,并与 DLBCL 中的高增殖肿瘤相关,这可能依赖于 GC 或 nGC 亚类。此外,在我们的系列中,它不是 R-CHOP 治疗疗效的标志物。

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