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通过全基因组表达谱对髓母细胞瘤进行分子分类

Molecular Classification of Medullobastomas by Whole Genome Expression Profiling.

作者信息

Nosková H, Adamcová S, Knoflíčková L D Radová, Pavelka Z, Vejmělková K, Zitterbart K, Slabý O, Štěrba J

出版信息

Klin Onkol. 2019 Spring;32(Supplementum1):171-173.

Abstract

BACKGROUND

Medulloblastoma (MB) is the most common malignant tumour of the central nervous system in children. MB is considered to be high risk tumour propensity to metastasize. In the Czech Republic, approximately 10-12 children are affected annually by this tumour. Recent progress in molecular diagnostics helps to refine the diagnosis and estimate clinical prognosis of the disease. Currently, MBs are subclassified into WNT-activated, SHH-activated, group 3, and 4 based on molecular pathways that drive their tumorigenesis. Each subtype differs in its histopathology, clinical features, genomic changes and gene expressions. The aim of our study is to classify patients MBs into four basic molecular groups and compare our results with published data.

MATERIAL AND METHODS

In our study we analysed expression profiles using Affymetrix GeneChip Human Gene 1.0. ST Array (Thermo Fisher Scientific, MA, USA). As input material RNA extracted from the fresh frozen tissue was used. Molecular classification based on the method established by P. Northcott in 2011 was performed.

RESULTS

From April 2015 to February 2019, 21 patients with MBs were included in our study. Median age of the patients at the time of diagnosis was 6 years, 14 boys and 7 girls were enrolled. Gene expression profiling and molecular classification of MBs was performed. Based on this methodology, we found the most frequently represented subgroup of MB was group 4 (9 patients, 43%), followed by group 3 (5 patients, 24%), SHH-activated MB (4 patients, 19%) and the least represented subgroup was WNT-activated MB (3 patients, 14%). Results of molecular subgroup classification of MBs were successfully correlated with histopathological findings and other molecular-genetic examinations.

CONCLUSION

Molecular classification of MBs has been established in our institution allowing better understanding of this heterogeneous disease and helping clinicians in therapeutic planning in affected patients. This work was supported by the Czech Ministry of Health grant No. 16-33209A. All rights reserved.  he authors declare they have no potential confl icts of interest concerning drugs, products, or services used in the study. The Editorial Board declares that the manuscript met the ICMJE recommendation for biomedical papers. Submitted: 1. 3. 2019 Accepted: 4. 3. 2019.

摘要

背景

髓母细胞瘤(MB)是儿童中枢神经系统最常见的恶性肿瘤。MB被认为是具有高转移倾向的肿瘤。在捷克共和国,每年约有10 - 12名儿童受此肿瘤影响。分子诊断方面的最新进展有助于完善该疾病的诊断并评估临床预后。目前,根据驱动其肿瘤发生的分子途径,MB被细分为WNT激活型、SHH激活型、3组和4组。各亚型在组织病理学、临床特征、基因组变化和基因表达方面存在差异。我们研究的目的是将MB患者分为四个基本分子组,并将我们的结果与已发表的数据进行比较。

材料与方法

在我们的研究中,我们使用Affymetrix GeneChip Human Gene 1.0 ST Array(美国马萨诸塞州赛默飞世尔科技公司)分析表达谱。以从新鲜冷冻组织中提取的RNA作为输入材料。基于P. Northcott在2011年建立的方法进行分子分类。

结果

2015年4月至2019年2月,21例MB患者纳入我们的研究。诊断时患者的中位年龄为6岁,纳入14名男孩和7名女孩。对MB进行了基因表达谱分析和分子分类。基于此方法,我们发现MB中最常见的亚组是4组(9例患者,43%),其次是3组(5例患者,24%),SHH激活型MB(4例患者,19%),最少见的亚组是WNT激活型MB(3例患者,14%)。MB的分子亚组分类结果与组织病理学发现及其他分子遗传学检查成功相关。

结论

我们机构已建立MB的分子分类,这有助于更好地理解这种异质性疾病,并帮助临床医生为受影响患者制定治疗计划。本研究得到捷克卫生部16 - 33209A号资助。保留所有权利。作者声明他们在研究中使用的药物、产品或服务方面不存在潜在利益冲突。编辑委员会声明该手稿符合ICMJE关于生物医学论文 的建议。提交日期:2019年3月1日;接受日期:2019年3月4日。

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