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牙源性黏液瘤中存在复发性拷贝数改变和独特的甲基化特征。

Odontogenic Myxomas Harbor Recurrent Copy Number Alterations and a Distinct Methylation Signature.

机构信息

Department of Pathology and Medical Biology, University Medical Center Groningen, Groningen, Netherlands.

Bone Tumor Reference Center, Institute for Medical Genetics and Pathology, University Hospital Basel, University of Basel, Basel, Switzerland.

出版信息

Am J Surg Pathol. 2024 Oct 1;48(10):1224-1232. doi: 10.1097/PAS.0000000000002293. Epub 2024 Oct 16.

Abstract

Odontogenic myxoma is a rare, benign, and locally aggressive tumor that develops in the tooth-bearing areas of the jaw. The molecular mechanisms underlying odontogenic myxomas are unknown and no diagnostic markers are available to date. The aim of this study was to analyze DNA methylation and copy number variations in odontogenic myxomas to identify new molecular signatures for diagnostic decision-making. We collected a cohort of 16 odontogenic myxomas from 2006 to 2021 located in the mandible (n = 10) and maxilla (n = 6) with available formalin-fixed paraffin-embedded or fresh frozen tumor tissue from a biopsy or resection material. Genome-wide DNA methylation and copy number variation data were generated from 12 odontogenic myxomas using the Illumina Infinium Methylation EPIC array, interrogating >850,000 CpG sites. Unsupervised clustering and dimensionality reduction (Uniform Manifold Approximation and Projection) revealed that odontogenic myxomas formed a distinct DNA methylation class. Copy number profiling showed recurrent whole-chromosome gains (trisomies) of chromosomes 5, 8, and 20 in all cases, and of chromosomes 10, 12, and 17 in all except one case. In conclusion, odontogenic myxomas harbor recurrent copy number patterns and a distinct DNA methylation profile, which can be used as an additional diagnostic tool in the appropriate clinical and radiologic context. Further research is needed to explain the genetic mechanisms caused by these alterations that drive these locally aggressive neoplasms.

摘要

牙源性黏液瘤是一种罕见的良性、局部侵袭性肿瘤,发生于颌骨的牙齿生长区域。牙源性黏液瘤的分子机制尚不清楚,也没有诊断标志物。本研究旨在分析牙源性黏液瘤的 DNA 甲基化和拷贝数变异,以确定新的分子特征用于诊断决策。我们收集了 2006 年至 2021 年间位于下颌骨(n=10)和上颌骨(n=6)的 16 例牙源性黏液瘤的队列,有可用的福尔马林固定石蜡包埋或新鲜冷冻肿瘤组织,来自活检或切除材料。使用 Illumina Infinium Methylation EPIC 阵列从 12 例牙源性黏液瘤中生成全基因组 DNA 甲基化和拷贝数变异数据,检测 >850,000 个 CpG 位点。无监督聚类和降维(一致流形逼近和投影)显示牙源性黏液瘤形成了一个独特的 DNA 甲基化类群。拷贝数分析显示所有病例均存在染色体 5、8 和 20 的全染色体增益(三体),除 1 例外,所有病例均存在染色体 10、12 和 17 的全染色体增益。总之,牙源性黏液瘤具有反复出现的拷贝数模式和独特的 DNA 甲基化谱,可以作为适当的临床和影像学背景下的附加诊断工具。需要进一步研究来解释这些改变导致这些局部侵袭性肿瘤的遗传机制。

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