DNA 甲基化是鉴别诊断 T-LBL 和富含淋巴细胞胸腺瘤的新工具。

IF 5.6 2区 医学 Q1 ONCOLOGY The Journal of Pathology Pub Date : 2024-09-27 DOI:10.1002/path.6346
Mehdi Latiri, Mohamed Belhocine, Charlotte Smith, Nathalie Garnier, Estelle Balducci, Antoine Pinton, Guillaume P Andrieu, Julie Bruneau, Salvatore Spicuglia, Stéphane Jamain, Violaine Latapie, Vincent Thomas de Montpreville, Lara Chalabreysse, Alexander Marx, Nicolas Girard, Benjamin Besse, Christoph Plass, Laure Gibault, Cécile Badoual, Elizabeth Macintyre, Vahid Asnafi, Thierry Jo Molina, Aurore Touzart
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引用次数: 0

摘要

T淋巴母细胞淋巴瘤(T-LBL)和胸腺瘤是两种罕见的胸腺原发性肿瘤,分别来自T细胞前体或胸腺上皮细胞。一些胸腺瘤亚型(AB、B1 和 B2)显示大量反应性末端脱氧核苷酸转移酶阳性(TdT+)的 T 细胞前体,掩盖了上皮肿瘤细胞。因此,T-LBL 与富含 TdT+ T 淋巴细胞的胸腺瘤之间的鉴别诊断具有挑战性,尤其是在针刺活检的情况下。为了区分T-LBL和胸腺瘤相关淋巴细胞增生,我们采用了两种不同的技术,即MeDIP阵列和EPIC阵列,分析了独立样本系列(分别是17例T-LBL与1例TdT+淋巴细胞丰富型胸腺瘤(B1亚型)和3例正常胸腺的比较,以及7例淋巴细胞丰富型胸腺瘤与24例T-LBL的比较)的全局DNA甲基化情况。在无监督主成分分析(PCA)中,T-LBL样本和胸腺瘤样本分别聚类。我们利用MeDIP-array和EPIC-array数据集确定了差异甲基化区域(DMRs),并考虑到前100个DMRs,确定了两个数据集之间的9个重叠基因,包括ZIC1、TSHZ2、CDC42BPB、RBM24、C10orf53和MACROD2。为了在更大的系列中探索DNA甲基化图谱,我们根据这六个不同甲基化的基因启动子定义了一个分类器,开发了一种MS-MLPA检测方法,并证明胸腺瘤(低甲基化;n = 48)和T-LBLs(高甲基化;n = 54)之间存在显著的甲基化差异(甲基化比值中位数分别为0.03和0.66;p<0.05)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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DNA methylation as a new tool for the differential diagnosis between T-LBL and lymphocyte-rich thymoma

T-lymphoblastic lymphoma (T-LBL) and thymoma are two rare primary tumors of the thymus deriving either from T-cell precursors or from thymic epithelial cells, respectively. Some thymoma subtypes (AB, B1, and B2) display numerous reactive terminal deoxynucleotidyl transferase-positive (TdT+) T-cell precursors masking epithelial tumor cells. Therefore, the differential diagnosis between T-LBL and TdT+ T-lymphocyte-rich thymoma could be challenging, especially in the case of needle biopsy. To distinguish between T-LBL and thymoma-associated lymphoid proliferations, we analyzed the global DNA methylation using two different technologies, namely MeDIP array and EPIC array, in independent samples series [17 T-LBLs compared with one TdT+ lymphocyte-rich thymoma (B1 subtype) and three normal thymi, and seven lymphocyte-rich thymomas compared with 24 T-LBLs, respectively]. In unsupervised principal component analysis (PCA), T-LBL and thymoma samples clustered separately. We identified differentially methylated regions (DMRs) using MeDIP-array and EPIC-array datasets and nine overlapping genes between the two datasets considering the top 100 DMRs including ZIC1, TSHZ2, CDC42BPB, RBM24, C10orf53, and MACROD2. In order to explore the DNA methylation profiles in larger series, we defined a classifier based on these six differentially methylated gene promoters, developed an MS-MLPA assay, and demonstrated a significant differential methylation between thymomas (hypomethylated; n = 48) and T-LBLs (hypermethylated; n = 54) (methylation ratio median 0.03 versus 0.66, respectively; p < 0.0001), with MACROD2 methylation status the most discriminating. Using a machine learning strategy, we built a prediction model trained with the EPIC-array dataset and defined a cumulative score taking into account the weight of each feature. A score above or equal to 0.4 was predictive of T-LBL and conversely. Applied to the MS-MLPA dataset, this prediction model accurately predicted diagnoses of T-LBL and thymoma. © 2024 The Author(s). The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland.

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来源期刊
The Journal of Pathology
The Journal of Pathology 医学-病理学
CiteScore
14.10
自引率
1.40%
发文量
144
审稿时长
3-8 weeks
期刊介绍: The Journal of Pathology aims to serve as a translational bridge between basic biomedical science and clinical medicine with particular emphasis on, but not restricted to, tissue based studies. The main interests of the Journal lie in publishing studies that further our understanding the pathophysiological and pathogenetic mechanisms of human disease. The Journal of Pathology welcomes investigative studies on human tissues, in vitro and in vivo experimental studies, and investigations based on animal models with a clear relevance to human disease, including transgenic systems. As well as original research papers, the Journal seeks to provide rapid publication in a variety of other formats, including editorials, review articles, commentaries and perspectives and other features, both contributed and solicited.
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