Suppr超能文献

成神经管细胞瘤中的亚群特异性剪接。

Subgroup-specific alternative splicing in medulloblastoma.

机构信息

Division of Neurosurgery, Arthur & Sonia Labatt Brain Tumour Research Centre, The Hospital for Sick Children, Toronto, Ontario, Canada.

Program in Developmental & Stem Cell Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.

出版信息

Acta Neuropathol. 2012 Apr;123(4):485-499. doi: 10.1007/s00401-012-0959-7. Epub 2012 Feb 23.

Abstract

Medulloblastoma comprises four distinct molecular variants: WNT, SHH, Group 3, and Group 4. We analyzed alternative splicing usage in 14 normal cerebellar samples and 103 medulloblastomas of known subgroup. Medulloblastoma samples have a statistically significant increase in alternative splicing as compared to normal fetal cerebella (2.3-times; P < 6.47E-8). Splicing patterns are distinct and specific between molecular subgroups. Unsupervised hierarchical clustering of alternative splicing events accurately assigns medulloblastomas to their correct subgroup. Subgroup-specific splicing and alternative promoter usage was most prevalent in Group 3 (19.4%) and SHH (16.2%) medulloblastomas, while observed less frequently in WNT (3.2%), and Group 4 (9.3%) tumors. Functional annotation of alternatively spliced genes reveals overrepresentation of genes important for neuronal development. Alternative splicing events in medulloblastoma may be regulated in part by the correlative expression of antisense transcripts, suggesting a possible mechanism affecting subgroup-specific alternative splicing. Our results identify additional candidate markers for medulloblastoma subgroup affiliation, further support the existence of distinct subgroups of the disease, and demonstrate an additional level of transcriptional heterogeneity between medulloblastoma subgroups.

摘要

髓母细胞瘤包含四个不同的分子亚型

WNT、SHH、Group 3 和 Group 4。我们分析了 14 例正常小脑样本和 103 例已知亚组的髓母细胞瘤中的选择性剪接使用情况。与正常胎儿小脑相比,髓母细胞瘤样本中的选择性剪接显著增加(2.3 倍;P < 6.47E-8)。分子亚组之间的剪接模式明显且具有特异性。选择性剪接事件的无监督层次聚类可准确地将髓母细胞瘤分配到其正确的亚组。亚组特异性剪接和替代启动子使用在 Group 3(19.4%)和 SHH(16.2%)髓母细胞瘤中最为常见,而在 WNT(3.2%)和 Group 4(9.3%)肿瘤中则较少见。选择性剪接基因的功能注释显示,与神经元发育相关的基因过表达。髓母细胞瘤中选择性剪接事件可能部分受到反义转录本的表达相关性的调节,这表明了一种可能影响亚组特异性选择性剪接的机制。我们的结果确定了髓母细胞瘤亚组归属的其他候选标志物,进一步支持了该疾病存在不同亚组的存在,并证明了髓母细胞瘤亚组之间存在额外的转录异质性。

相似文献

1
Subgroup-specific alternative splicing in medulloblastoma.成神经管细胞瘤中的亚群特异性剪接。
Acta Neuropathol. 2012 Apr;123(4):485-499. doi: 10.1007/s00401-012-0959-7. Epub 2012 Feb 23.
3
Medulloblastoma comprises four distinct molecular variants.髓母细胞瘤包含四个不同的分子亚型。
J Clin Oncol. 2011 Apr 10;29(11):1408-14. doi: 10.1200/JCO.2009.27.4324. Epub 2010 Sep 7.
8
Rapid diagnosis of medulloblastoma molecular subgroups.快速诊断髓母细胞瘤分子亚型。
Clin Cancer Res. 2011 Apr 1;17(7):1883-94. doi: 10.1158/1078-0432.CCR-10-2210. Epub 2011 Feb 16.
10
[Subtypes of medulloblastomas: distinct cellular origins].[髓母细胞瘤的亚型:不同的细胞起源]
Med Sci (Paris). 2012 Oct;28(10):805-9. doi: 10.1051/medsci/20122810003. Epub 2012 Oct 12.

引用本文的文献

10
Gene Regulatory Network Perturbation by Genetic and Epigenetic Variation.基因调控网络的遗传和表观遗传变异扰动。
Trends Biochem Sci. 2018 Aug;43(8):576-592. doi: 10.1016/j.tibs.2018.05.002. Epub 2018 Jun 22.

本文引用的文献

2
p53 Family: Role of Protein Isoforms in Human Cancer.p53家族:蛋白质异构体在人类癌症中的作用
J Nucleic Acids. 2012;2012:687359. doi: 10.1155/2012/687359. Epub 2011 Oct 9.
4
Finding the perfect partner for medulloblastoma prognostication.寻找髓母细胞瘤预后评估的理想指标
J Clin Oncol. 2011 Oct 10;29(29):3841-2. doi: 10.1200/JCO.2011.37.5709. Epub 2011 Sep 12.
9
Subtypes of medulloblastoma have distinct developmental origins.髓母细胞瘤亚型具有不同的发育起源。
Nature. 2010 Dec 23;468(7327):1095-9. doi: 10.1038/nature09587. Epub 2010 Dec 8.
10
Molecular diagnostics in embryonal brain tumors.胚胎性脑肿瘤的分子诊断。
Brain Pathol. 2011 Jan;21(1):96-104. doi: 10.1111/j.1750-3639.2010.00455.x.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验