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儿童癌症髓母细胞瘤的遗传特征。

The genetic landscape of the childhood cancer medulloblastoma.

机构信息

Ludwig Center for Cancer Genetics and Therapeutics and Howard Hughes Medical Institute, Johns Hopkins Kimmel Cancer Center, Baltimore, MD 21231, USA.

出版信息

Science. 2011 Jan 28;331(6016):435-9. doi: 10.1126/science.1198056. Epub 2010 Dec 16.

Abstract

Medulloblastoma (MB) is the most common malignant brain tumor of children. To identify the genetic alterations in this tumor type, we searched for copy number alterations using high-density microarrays and sequenced all known protein-coding genes and microRNA genes using Sanger sequencing in a set of 22 MBs. We found that, on average, each tumor had 11 gene alterations, fewer by a factor of 5 to 10 than in the adult solid tumors that have been sequenced to date. In addition to alterations in the Hedgehog and Wnt pathways, our analysis led to the discovery of genes not previously known to be altered in MBs. Most notably, inactivating mutations of the histone-lysine N-methyltransferase genes MLL2 or MLL3 were identified in 16% of MB patients. These results demonstrate key differences between the genetic landscapes of adult and childhood cancers, highlight dysregulation of developmental pathways as an important mechanism underlying MBs, and identify a role for a specific type of histone methylation in human tumorigenesis.

摘要

髓母细胞瘤(MB)是儿童中最常见的恶性脑肿瘤。为了鉴定这种肿瘤类型的遗传改变,我们使用高密度微阵列寻找拷贝数改变,并使用 Sanger 测序对 22 例 MB 中的所有已知的蛋白编码基因和 microRNA 基因进行测序。我们发现,平均每个肿瘤有 11 个基因改变,比迄今测序的成人实体肿瘤少 5 到 10 倍。除了 Hedgehog 和 Wnt 通路的改变外,我们的分析还导致了发现以前在 MB 中未改变的基因。值得注意的是,在 16%的 MB 患者中发现了组蛋白-赖氨酸 N-甲基转移酶基因 MLL2 或 MLL3 的失活突变。这些结果表明成人和儿童癌症的遗传景观存在关键差异,突出了发育途径的失调是 MB 的重要机制,并确定了特定类型的组蛋白甲基化在人类肿瘤发生中的作用。

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