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首页> 外文期刊>Human Genetics >Molecular analysis of the TSC1 and TSC2 tumour suppressor genes in sporadic glial and glioneuronal tumours.
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Molecular analysis of the TSC1 and TSC2 tumour suppressor genes in sporadic glial and glioneuronal tumours.

机译:TSC1和TSC2肿瘤抑制基因在散发性神经胶质和神经胶质瘤中的分子分析。

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摘要

Reduced expression of the TSC2 tumour suppressor gene product, tuberin, has been reported in sporadic astrocytomas, suggesting that the TSC genes may play a role in formation of sporadic glial or glioneuronal tumours. We studied paired constitutional and tumour DNA samples from 100 patients with sporadic glial and glioneuronal tumours for loss of heterozygosity (LOH) at the TSC1 and TSC2 loci using a combination of seven previously reported and seven novel polymorphic markers. LOH was seen in 1/16 astrocytomas, 3/15 ependymomas, 5/16 gangliogliomas, 2/14 glioblastoma multiforme, 0/7 oligodendrogliomas, 0/7 tumours of mixed oligodendrocytic/astrocytic histology, 2/11 pilocytic astrocytomas and 0/1 subependymal giant cell astrocytomas informative at both loci. However, SSCP screening of all coding exons of the TSC1 or TSC2 genes in the tumours displaying LOH, and of both genes in 21 gangliogliomas, revealed no intragenic mutations. The lack of demonstrable inactivation of both alleles of either TSC gene in any of the tumours investigated suggests that they do not play a frequent role in the aetiology of sporadic glial or glioneuronal tumours.
机译:TSC2抑癌基因产物tuberin的表达在散发性星形细胞瘤中有降低的报道,这表明TSC基因可能在散发性神经胶质或神经胶质瘤的形成中起作用。我们使用七个先前报道的和七个新的多态性标记的组合,研究了来自100例散发性神经胶质和神经胶质瘤的患者的体质和肿瘤DNA样本,以了解TSC1和TSC2位点杂合性(LOH)的丧失。在1/16星形细胞瘤,3/15室管膜瘤,5/16神经胶质瘤,2/14多形胶质母细胞瘤,0/7少突神经胶质瘤,0/7少突神经胶质细胞/星形胶质细胞混合组织肿瘤,2/11毛细胞星形细胞瘤和0/1中发现了LOH室管膜下巨细胞星形细胞瘤在两个基因座处都提供信息。然而,对显示LOH的肿瘤中TSC1或TSC2基因的所有编码外显子以及21个神经节神经胶质瘤中的两个基因的SSCP筛选均未发现基因内突变。在所研究的任何肿瘤中,任一TSC基因的两个等位基因均未显示出明显的失活,这表明它们在散发性神经胶质或神经胶质瘤的病因学中并不经常发挥作用。

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