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首页> 外文期刊>The Southeast Asian journal of tropical medicine and public health >Malignant glioma: the involvement of loss of allelic heterozygosity and PTEN mutations in a group of Malay patients.
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Malignant glioma: the involvement of loss of allelic heterozygosity and PTEN mutations in a group of Malay patients.

机译:恶性神经胶质瘤:一组马来患者等位基因杂合性丧失和PTEN突变。

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摘要

Frequent loss of heterozygosity (LOH) and mutations of the tumor suppressor gene PTEN (phosphatase and tensin homologue deleted from chromosome 10) have been found in sporadic gliomas. The most documented regions of allelic losses include 9p21, 10q23-25 and 17p1 3 whereas PTEN aberrations are preferentially found in glioblastoma multiformes. This research aimed to detect the incidence of allelic losses on chromosomes 10q, 9p, 17p and 13q and mutations on exons 5, 6 and 8 of PTEN in malignant gliomas. Malignant glioma specimens obtained were classified histopathologically according to the WHO criteria. Each tumor was then subjected to polymerase chain reaction (PCR)-LOH analysis using microsatellite markers and single-stranded conformational polymorphism (SSCP) analysis. Twelve of 23 (52%) malignant glioma cases showed allelic losses whereas 7 of 23 (30%) samples showed aberrant band patterns and mutations of PTEN. Four of these cases showed LOH in 10q23 and mutations of PTEN. The data on LOH indicated the involvement of different genes in the genesis of glioma whereas mutations of PTEN indicated the role of PTEN tumor suppressor gene in the progression of glioma in Malay population.
机译:在散发性神经胶质瘤中,经常发现杂合子缺失(LOH)和肿瘤抑制基因PTEN的突变(从10号染色体上删除的磷酸酶和张力蛋白同源物)。等位基因丢失的最有记录的区域包括9p21、10q23-25和17p13,而PTEN畸变则优先出现在多形性胶质母细胞瘤中。这项研究旨在检测恶性神经胶质瘤中10q,9p,17p和13q染色体等位基因缺失的发生率以及PTEN外显子5、6和8的突变。根据WHO标准对获得的恶性神经胶质瘤标本进行组织病理学分类。然后使用微卫星标记和单链构象多态性(SSCP)分析每个肿瘤的聚合酶链反应(PCR)-LOH。 23例(52%)恶性神经胶质瘤病例中有12例显示等位基因缺失,而23例(30%)样本中有7例显示异常条带模式和PTEN突变。这些病例中有4个在10q23中显示出LOH和PTEN突变。 LOH的数据表明,不同基因参与了胶质瘤的发生,而PTEN的突变表明,PTEN抑癌基因在马来人胶质瘤的进展中具有重要作用。

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