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NOTCH3 外显子 16 的表达将弥漫性大 B 细胞淋巴瘤分为分子亚型,并与预后相关。

Expression of NOTCH3 exon 16 differentiates Diffuse Large B-cell Lymphoma into molecular subtypes and is associated with prognosis.

机构信息

Department of Hematology, Aalborg University Hospital, Aalborg, Denmark.

Department of Clinical Medicine, Aalborg University, Aalborg, Denmark.

出版信息

Sci Rep. 2019 Jan 23;9(1):335. doi: 10.1038/s41598-018-36680-x.

Abstract

Diffuse large B-cell lymphoma (DLBCL) is a heterogeneous disease with diverse clinical presentation and outcome. Bio-clinical prognostic models including oncogene expression and cell-of-origin phenotyping has been developed, however, approximately 30% of all patients still die from their disease, illustrating the need for additional prognostic biomarkers associating oncogenesis and phenotypic subclasses. Hence, we tested if alternative splice variations have biomarker potential. Initial alternative splicing analysis of human exon array from clinical DLBCL samples identified candidate genes. Experimental validation by ddPCR was performed in a DLBCL cohort classified into ABC/GCB subclasses, B-cell associated gene signatures (BAGS: naive, centroblast, centrocyte, memory, and plasmablast), and vincristine resistant gene signatures. Prognostic potential was assessed for aberrantly spliced transcripts. Thus, NOTCH3 was identified as alternatively spliced, with differential exon 16 depletion (-exon 16) between differentiation associated BAGS subtypes. Predicted vincristine resistant patients of the GCB subclass had significantly downregulated NOTCH3 -exon 16 transcript expression and tended to display adverse overall survival for R-CHOP treated patients. In conclusion, we have identified a specific alternatively spliced NOTCH3 event that differentiate molecular subtypes of DLBCL and display prognostic and predictive biomarker potential in GCB DLBCL.

摘要

弥漫性大 B 细胞淋巴瘤(DLBCL)是一种具有不同临床表现和结局的异质性疾病。已经开发了包括癌基因表达和细胞起源表型的生物临床预后模型,然而,大约 30%的所有患者仍死于该疾病,这表明需要额外的与致癌基因和表型亚类相关的预后生物标志物。因此,我们测试了是否存在其他剪接变异具有生物标志物潜力。从临床 DLBCL 样本的人类外显子数组进行初始的选择性剪接分析,确定了候选基因。通过 ddPCR 在 ABC/GCB 亚类分类的 DLBCL 队列中进行了实验验证,以及 B 细胞相关基因特征(幼稚、中心母细胞、中心细胞、记忆和浆母细胞)和长春新碱耐药基因特征。对异常剪接的转录本进行了预后潜力评估。因此,NOTCH3 被鉴定为选择性剪接,在与分化相关的 BAGS 亚型中存在不同的外显子 16 缺失(-exon 16)。GCB 亚类中预测的长春新碱耐药患者的 NOTCH3-exon 16 转录本表达明显下调,并且倾向于显示出 R-CHOP 治疗患者的不良总生存。总之,我们已经确定了一种特定的选择性剪接 NOTCH3 事件,该事件可区分 DLBCL 的分子亚型,并在 GCB DLBCL 中显示出预后和预测生物标志物潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c678/6344585/d1b6f68d7ec5/41598_2018_36680_Fig1_HTML.jpg

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