Suppr超能文献

EB 病毒诱导基因 3(EBI3):伯基特淋巴瘤和弥漫性大 B 细胞淋巴瘤的新型诊断标志物。

Epstein-Barr virus-induced gene 3 (EBI3): a novel diagnosis marker in Burkitt lymphoma and diffuse large B-cell lymphoma.

机构信息

CNRS UMR 8147, Université Paris Descartes, Sorbonne Paris Cité, Paris, France.

出版信息

PLoS One. 2011;6(9):e24617. doi: 10.1371/journal.pone.0024617. Epub 2011 Sep 8.

Abstract

The distinction between Burkitt lymphoma (BL) and diffuse large B-cell lymphoma (DLBCL), two types of mature aggressive B-cell lymphomas that require distinct treatments, can be difficult because of forms showing features intermediate between DLBCL and BL (here called BL/DLBCL). They can be discriminated by the presence of c-myc translocations characteristic of BL. However, these are not exclusive of BL and when present in DLBCL are associated with lower survival. In this study, we show that Epstein-Barr virus-induced gene 3 (EBI3) is differentially expressed among BL and DLBCL. Analysis of gene expression data from 502 cases of aggressive mature B-cell lymphomas available on Gene Expression Omnibus and immunohistochemical analysis of 184 cases of BL, BL/DLBCL or DLBCL, showed that EBI3 was not expressed in EBV-positive or -negative BL cases, whereas it was expressed by over 30% of tumoral cells in nearly 80% of DLBCL cases, independently of their subtypes. In addition, we show that c-myc overexpression represses EBI3 expression, and that DLBCL or BL/DLBCL cases with c-myc translocations have lower expression of EBI3. Thus, EBI3 immunohistochemistry could be useful to discriminate BL from DLBCL, and to identify cases of BL/DLBCL or DLBCL with potential c-myc translocations.

摘要

伯基特淋巴瘤 (BL) 和弥漫性大 B 细胞淋巴瘤 (DLBCL) 是两种成熟侵袭性 B 细胞淋巴瘤,需要不同的治疗方法,由于表现出介于 DLBCL 和 BL 之间特征的形式,两者之间的区分可能很困难 (这里称为 BL/DLBCL)。这些特征可以通过存在特征性的 BL 易位来区分。然而,这些并非 BL 所特有,并且当存在于 DLBCL 中时与较低的存活率相关。在这项研究中,我们表明 EBV 诱导基因 3 (EBI3) 在 BL 和 DLBCL 之间存在差异表达。对 Gene Expression Omnibus 上 502 例侵袭性成熟 B 细胞淋巴瘤的基因表达数据进行分析,并对 184 例 BL、BL/DLBCL 或 DLBCL 进行免疫组化分析,结果表明 EBV 阳性或阴性 BL 病例中不表达 EBI3,而在近 80%的 DLBCL 病例中,超过 30%的肿瘤细胞表达 EBI3,而与其亚型无关。此外,我们还表明 c-myc 过表达抑制 EBI3 的表达,并且具有 c-myc 易位的 BL/DLBCL 或 DLBCL 病例 EBI3 的表达水平较低。因此,EBI3 免疫组化可用于区分 BL 和 DLBCL,并识别可能具有 c-myc 易位的 BL/DLBCL 或 DLBCL 病例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2a8/3169615/ad5728df228b/pone.0024617.g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验