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Prevalence of copy-number neutral LOH in glioblastomas revealed by genomewide analysis of laser-microdissected tissues

机译:全基因组激光显微切割组织分析揭示胶质母细胞瘤中拷贝数中性LOH的患病率

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We have employed a laser-capture microdissection technique and single-nucleotide polymorphism arrays to characterize genomic alterations associated with the development of glioblastoma multiforme (GBM). Combined analysis of loss of heterozygosity (LOH) and copy number revealed that more than half (56.3%) of the 254 identified LOH loci showed no copy-number alteration, indicating the presence of copy-number neutral LOH (cnLOH). Furthermore, we found a GBM case that showed cnLOH in 18 of the 22 autosomes. These results were confirmed by quantitative real-time PCR, microsat-ellite analysis, and fluorescence in situ hybridization. The high rate of cnLOH suggests that epigenetic abnormalities of many genes are involved in the development and progression of GBMs.
机译:我们已经采用了激光捕获显微切割技术和单核苷酸多态性阵列来表征与多形性胶质母细胞瘤(GBM)的发展相关的基因组改变。杂合性丧失(LOH)和拷贝数的综合分析显示,在254个已鉴定的LOH基因座中,超过一半(56.3%)没有拷贝数变化,表明存在拷贝数中性LOH(cnLOH)。此外,我们发现了一个GBM病例,在22个常染色体中的18个中显示cnLOH。这些结果已通过实时定量PCR,微卫星分析和荧光原位杂交得到了证实。 cnLOH的高发病率提示许多基因的表观遗传异常与GBM的发生和发展有关。

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