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结外边缘区淋巴瘤:基因表达和 miRNA 谱分析鉴定诊断标志物和潜在治疗靶点。

Nodal marginal zone lymphoma: gene expression and miRNA profiling identify diagnostic markers and potential therapeutic targets.

机构信息

Virgen de la Salud Hospital, Toledo, Spain.

出版信息

Blood. 2012 Jan 19;119(3):e9-e21. doi: 10.1182/blood-2011-02-339556. Epub 2011 Nov 22.

Abstract

Nodal marginal zone lymphoma (NMZL) is a small B-cell neoplasm whose molecular pathogenesis is still essentially unknown and whose differentiation from other small B-cell lymphomas is hampered by the lack of specific markers. We have analyzed gene expression, miRNA profile, and copy number data from 15 NMZL cases. For comparison, 16 follicular lymphomas (FLs), 9 extranodal marginal zone lymphomas, and 8 reactive lymph nodes and B-cell subtypes were included. The results were validated by quantitative RT-PCR in an independent series, including 61 paraffin-embedded NMZLs. NMZL signature showed an enriched expression of gene sets identifying interleukins, integrins, CD40, PI3K, NF-κB, and TGF-β, and included genes expressed by normal marginal zone cells and memory B cells. The most highly overexpressed genes were SYK, TACI, CD74, CD82, and CDC42EP5. Genes linked to G(2)/M and germinal center were down-regulated. Comparison of the gene expression profiles of NMZL and FL showed enriched expression of CHIT1, TGFB1, and TACI in NMZL, and BCL6, LMO2, and CD10 in FL. NMZL displayed increased expression of miR-221, miR-223, and let-7f, whereas FL strongly expressed miR-494. Our study identifies new candidate diagnostic molecules for NMZL and reveals survival pathways activated in NMZL.

摘要

结外黏膜边缘区淋巴瘤(NMZL)是一种小 B 细胞肿瘤,其分子发病机制尚不清楚,由于缺乏特异性标志物,其与其他小 B 细胞淋巴瘤的区分受到阻碍。我们分析了 15 例 NMZL 病例的基因表达、miRNA 谱和拷贝数数据。为了比较,还包括 16 例滤泡性淋巴瘤(FL)、9 例结外黏膜边缘区淋巴瘤和 8 例反应性淋巴结和 B 细胞亚型。结果在一个独立的系列中通过定量 RT-PCR 进行了验证,包括 61 例石蜡包埋的 NMZL。NMZL 特征显示识别白细胞介素、整合素、CD40、PI3K、NF-κB 和 TGF-β的基因集表达丰富,并包括正常边缘区细胞和记忆 B 细胞表达的基因。表达最高的基因是 SYK、TACI、CD74、CD82 和 CDC42EP5。与 G(2)/M 和生发中心相关的基因下调。NMZL 和 FL 的基因表达谱比较显示,NMZL 中 CHIT1、TGFB1 和 TACI 表达丰富,而 FL 中 BCL6、LMO2 和 CD10 表达丰富。NMZL 显示 miR-221、miR-223 和 let-7f 的表达增加,而 FL 则强烈表达 miR-494。我们的研究为 NMZL 确定了新的候选诊断分子,并揭示了 NMZL 中激活的生存途径。

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