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Deep intronic hotspot variant explaining rhabdoid tumor predisposition syndrome in two patients with atypical teratoid and rhabdoid tumor.深度内含子热点变异解释了两名非典型畸胎样和横纹肌样瘤患者的横纹肌样瘤易感综合征。
Eur J Hum Genet. 2017 Oct;25(10):1170-1172. doi: 10.1038/ejhg.2017.115. Epub 2017 Jul 19.
2
Cancer Surveillance in Gorlin Syndrome and Rhabdoid Tumor Predisposition Syndrome.戈林综合征和横纹肌样瘤易感综合征的癌症监测
Clin Cancer Res. 2017 Jun 15;23(12):e62-e67. doi: 10.1158/1078-0432.CCR-17-0595.
3
Genome-Wide Profiles of Extra-cranial Malignant Rhabdoid Tumors Reveal Heterogeneity and Dysregulated Developmental Pathways.颅外恶性横纹肌样肿瘤的全基因组特征揭示了其异质性和发育途径失调。
Cancer Cell. 2016 Mar 14;29(3):394-406. doi: 10.1016/j.ccell.2016.02.009.
4
Atypical Teratoid/Rhabdoid Tumors Are Comprised of Three Epigenetic Subgroups with Distinct Enhancer Landscapes.非典型畸胎样/横纹肌样肿瘤由三个具有不同增强子景观的表观遗传亚群组成。
Cancer Cell. 2016 Mar 14;29(3):379-393. doi: 10.1016/j.ccell.2016.02.001. Epub 2016 Feb 25.
5
Molecular subgroups of atypical teratoid rhabdoid tumours in children: an integrated genomic and clinicopathological analysis.儿童非典型畸胎样横纹肌样肿瘤的分子亚型:基因组与临床病理综合分析。
Lancet Oncol. 2015 May;16(5):569-82. doi: 10.1016/S1470-2045(15)70114-2. Epub 2015 Apr 14.
6
SMARCA4-mutated atypical teratoid/rhabdoid tumors are associated with inherited germline alterations and poor prognosis.SMARCA4突变的非典型畸胎样/横纹肌样肿瘤与遗传性种系改变及预后不良相关。
Acta Neuropathol. 2014 Sep;128(3):453-6. doi: 10.1007/s00401-014-1323-x. Epub 2014 Jul 25.
7
Minfi: a flexible and comprehensive Bioconductor package for the analysis of Infinium DNA methylation microarrays.Minfi:一个用于分析 Infinium DNA 甲基化微阵列的灵活且全面的 Bioconductor 软件包。
Bioinformatics. 2014 May 15;30(10):1363-9. doi: 10.1093/bioinformatics/btu049. Epub 2014 Jan 28.
8
Pediatric rhabdoid tumors of kidney and brain show many differences in gene expression but share dysregulation of cell cycle and epigenetic effector genes.小儿肾和脑横纹肌样瘤在基因表达上存在许多差异,但存在细胞周期和表观遗传效应基因的失调。
Pediatr Blood Cancer. 2013 Jul;60(7):1095-102. doi: 10.1002/pbc.24481. Epub 2013 Feb 4.
9
High-resolution genomic analysis suggests the absence of recurrent genomic alterations other than SMARCB1 aberrations in atypical teratoid/rhabdoid tumors.高分辨率基因组分析提示,在非典型畸胎瘤/横纹肌样瘤中除 SMARCB1 异常外不存在其他复发性基因组改变。
Genes Chromosomes Cancer. 2013 Feb;52(2):185-90. doi: 10.1002/gcc.22018. Epub 2012 Oct 17.
10
A remarkably simple genome underlies highly malignant pediatric rhabdoid cancers.高度恶性的小儿横纹肌肉瘤的基因组基础出人意料地简单。
J Clin Invest. 2012 Aug;122(8):2983-8. doi: 10.1172/JCI64400. Epub 2012 Jul 17.

中枢神经系统内外的恶性横纹肌样肿瘤在临床上和分子上具有异质性。

Malignant rhabdoid tumors originating within and outside the central nervous system are clinically and molecularly heterogeneous.

机构信息

Department of Pathology, St. Jude Children's Research Hospital, 262 Danny Thomas Place, Memphis, TN, 38105, USA.

Department of Oncology, St. Jude Children's Research Hospital, 262 Danny Thomas Place, Memphis, TN, 38105, USA.

出版信息

Acta Neuropathol. 2018 Aug;136(2):315-326. doi: 10.1007/s00401-018-1814-2. Epub 2018 Feb 10.

DOI:10.1007/s00401-018-1814-2
PMID:29428974
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6063764/
Abstract

Multifocal synchronous or metachronous atypical teratoid rhabdoid tumors (ATRTs) and non-central nervous system malignant rhabdoid tumors (extra-CNS MRTs) are rare cancers. We reviewed the clinical and radiologic characteristics of affected patients seen at our institution. Genotyping and analysis of copy number abnormalities (CNAs) in SMARCB1 were performed in germline and tumor samples. Tumor samples underwent genome-wide DNA methylation and CNA analysis. The median age at diagnosis of 21 patients was 0.6 years. Two-thirds of ATRTs and extra-CNS MRTs were diagnosed synchronously. Although kidney tumors predominated, including two patients with bilateral involvement, at least 30% of cases lacked renal involvement. Histopathologic review confirmed MRTs in all cases and INI1 expression loss in all tumors tested. Fourteen (78%) of 18 patients tested had heterozygous germline SMARCB1 abnormalities. At least one allelic SMARCB1 abnormality was confirmed in 81 and 88% of ATRTs and extra-CNS MRTs, respectively. Unsupervised hierarchical clustering analysis of DNA methylation in 27 tumors and comparison with a reference group of 150 ATRTs classified the CNS tumors (n = 14) as sonic hedgehog (64%), tyrosinase (21%), and MYC (14%). The MYC subgroup accounted for 85% of 13 extra-CNS MRTs. Of 16 paired ATRTs and extra-CNS MRTs, the tumors in seven of eight patients showed a different pattern of genome-wide DNA methylation and/or CNAs suggestive of non-clonal origin. CNS and extra-CNS tumors had an identical SMARCB1 amplification (n = 1) or very similar DNA methylation pattern (n = 1) suggestive of clonal origin. All patients died of tumor progression. The clinical and molecular characteristics of multifocal ATRTs and extra-CNS MRTs are heterogeneous with most patients harboring a cancer predisposition. Although independent tumor origin was confirmed in most cases, metastatic spread was also documented. The recognition of their distinct molecular characteristics is critical in selecting new biologic therapies against these deadly cancers.

摘要

多灶性同步或异时性非典型性畸胎样横纹肌样肿瘤(ATRTs)和非中枢神经系统恶性横纹肌样肿瘤(extra-CNS MRTs)是罕见的癌症。我们回顾了在我们机构就诊的受影响患者的临床和影像学特征。在生殖系和肿瘤样本中进行了 SMARCB1 的基因分型和拷贝数异常(CNAs)分析。肿瘤样本进行了全基因组 DNA 甲基化和 CNA 分析。21 名患者的中位诊断年龄为 0.6 岁。三分之二的 ATRTs 和 extra-CNS MRTs 是同步诊断的。尽管肾脏肿瘤占主导地位,包括两名双侧受累的患者,但至少 30%的病例没有肾脏受累。组织病理学复查证实所有病例均为 MRT,所有肿瘤均检测到 INI1 表达缺失。在 18 名接受测试的患者中,有 14 名(78%)存在杂合性生殖系 SMARCB1 异常。至少有一个等位基因 SMARCB1 异常在 ATRTs 和 extra-CNS MRTs 中分别被证实分别为 81%和 88%。对 27 个肿瘤的 DNA 甲基化进行无监督层次聚类分析,并与 150 个 ATRTs 的参考组进行比较,将中枢神经系统肿瘤(n=14)分为 sonic hedgehog(64%)、酪氨酸酶(21%)和 MYC(14%)。MYC 亚组占 13 例 extra-CNS MRTs 的 85%。在 16 对配对的 ATRTs 和 extra-CNS MRTs 中,8 名患者中有 7 名患者的肿瘤显示出不同的全基因组 DNA 甲基化和/或 CNA 模式,提示非克隆起源。中枢神经系统和 extra-CNS 肿瘤具有相同的 SMARCB1 扩增(n=1)或非常相似的 DNA 甲基化模式(n=1),提示克隆起源。所有患者均因肿瘤进展而死亡。多灶性 ATRTs 和 extra-CNS MRTs 的临床和分子特征具有异质性,大多数患者存在癌症易感性。尽管在大多数情况下证实了独立的肿瘤起源,但也记录了转移扩散。认识到它们独特的分子特征对于选择针对这些致命癌症的新生物学治疗方法至关重要。