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新型甲基化模式可预测葡萄膜黑色素瘤的预后。

Novel Methylation Patterns Predict Outcome in Uveal Melanoma.

作者信息

Ferrier Sarah Tadhg, Burnier Julia Valdemarin

机构信息

Cancer Research Program, Research Institute of the McGill University Health Centre, Montreal, QC H4A 3J1, Canada.

Experimental Pathology Unit, Department of Pathology, McGill University, Montreal, QC H3A 0G4, Canada.

出版信息

Life (Basel). 2020 Oct 20;10(10):248. doi: 10.3390/life10100248.

Abstract

Uveal melanoma (UM) is the most common intraocular tumor in adults. Despite effective local treatments, 50% of patients develop metastasis. Better ways to determine prognosis are needed as well as new therapeutic targets. Epigenetic changes are important events driving cancer progression; however, few studies exist on methylation changes in UM. Our aim was to identify methylation events associated with UM prognosis. Matched clinical, genetic, and methylation data for 80 UM cases were obtained from The Cancer Genome Atlas (TCGA). Top differentially methylated loci were sorted through hierarchical clustering based on methylation patterns, and these patterns were compared to tumor characteristics, genomic aberrations, and patient outcome. Hierarchical clustering revealed two distinct groups. These classifications effectively separated high and low-risk cases, with significant differences between groups in patient survival ( < 0.0001) and correlation with known prognostic factors. Major differences in methylation of specific genes, notably , , and , were also seen. The methylation patterns identified in this study indicate potential novel prognostic indicators of UM and highlight the power of methylation changes in predicting outcome. The methylation events enriched in the high-risk group suggest that epigenetic modulating drugs may be useful in reducing metastatic potential, and that specific differentially methylated loci could act as biomarkers of therapeutic response.

摘要

葡萄膜黑色素瘤(UM)是成人中最常见的眼内肿瘤。尽管有有效的局部治疗方法,但仍有50%的患者会发生转移。因此需要更好的方法来确定预后以及新的治疗靶点。表观遗传变化是驱动癌症进展的重要事件;然而,关于UM甲基化变化的研究很少。我们的目的是确定与UM预后相关的甲基化事件。从癌症基因组图谱(TCGA)获得了80例UM病例的匹配临床、遗传和甲基化数据。根据甲基化模式通过层次聚类对差异甲基化程度最高的位点进行排序,并将这些模式与肿瘤特征、基因组畸变和患者预后进行比较。层次聚类揭示了两个不同的组。这些分类有效地分离了高风险和低风险病例,两组在患者生存率(<0.0001)以及与已知预后因素的相关性方面存在显著差异。在特定基因的甲基化方面也观察到了主要差异,特别是[具体基因1]、[具体基因2]和[具体基因3]。本研究中确定的甲基化模式表明UM可能有新的预后指标,并突出了甲基化变化在预测预后方面的作用。高风险组中富集的甲基化事件表明,表观遗传调节药物可能有助于降低转移潜能,并且特定的差异甲基化位点可作为治疗反应的生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c835/7589184/8c0ba2f6834d/life-10-00248-g001.jpg

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