首页> 美国卫生研究院文献>American Journal of Human Genetics >Deletion mapping of gliomas suggest the presence of two small regions for candidate tumor-suppressor genes in a 17-cM interval on chromosome 10q.
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Deletion mapping of gliomas suggest the presence of two small regions for candidate tumor-suppressor genes in a 17-cM interval on chromosome 10q.

机译:胶质瘤的缺失作图表明在染色体10q的17-cM间隔中存在两个候选肿瘤抑制基因的小区域。

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摘要

The loss of genetic material on chromosome 10q is frequent in different tumors and particularly in malignant gliomas. We analyzed 90 of these tumors and found loss of heterozygosity (LOH) in >90% of the informative loci in glioblastoma multiforme (GBM). Initial studies restricted the common LOH region to 10q24-qter. Subsequently, the study of a pediatric GBM suggested D10S221 and D10S209, respectively, as centromeric and telomeric markers of a 4-cM LOH region. It is interesting to note that, in one subset of cells from this tumor, locus D10S209 seems involved in the allelic imbalance of a larger region, with D10S214 as telomeric marker. This 17-cM region contains the D10S587-D10S216 interval of common deletion recently defined on another set of gliomas.
机译:在10q染色体上遗传物质的丢失在不同的肿瘤中尤其是在恶性神经胶质瘤中很常见。我们分析了这些肿瘤中的90个,发现多形性胶质母细胞瘤(GBM)信息性基因座中> 90%的杂合性(LOH)丧失。初步研究将普通LOH区域限制在10q24-qter。随后,对儿科GBM的研究建议分别将D10S221和D10S209作为4-cM LOH区的着丝粒和端粒标记。有趣的是,在该肿瘤的一个细胞子集中,基因座D10S209似乎参与了较大区域的等位基因失衡,其中D10S214为端粒标记。这个17-cM区域包含最近在另一套神经胶质瘤上定义的常见缺失的D10S587-D10S216区间。

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