首页> 外文期刊>Cytogenetic and genome research >Narrowing down the Common Cytogenetic Deletion 14q to a 5.6-Mb Critical Region in 1p/19q Codeletion Oligodendroglioma-Relapsed Patients Points to Two Potential Relapse-Related Genes:SEL1LandSTON2
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Narrowing down the Common Cytogenetic Deletion 14q to a 5.6-Mb Critical Region in 1p/19q Codeletion Oligodendroglioma-Relapsed Patients Points to Two Potential Relapse-Related Genes:SEL1LandSTON2

机译:在1P / 19Q Codeletion Oligodendroglioma-复发患者中缩小常见的细胞遗传学缺失14Q至5.6Mb关键区域,分发到两个潜在的复发相关基因:Sel1landston2

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摘要

Based on a literature review and our database, we report on the smallest 14q deletion identified in a brain tumor characterized by 1p/19q codeletion low-grade oligodendroglioma. In 2013, array-comparative genomic hybridization of the brain tumor revealed 1p/19q codeletion as a sole abnormality. In 2019, the patient relapsed showing additional abnormalities including a 14q deletion of 16.5 Mb at 14q24.2q31.3. This region overlaps with 2 previously identified minimal regions, 14q21.2q24.3 and 14q31.3q32.1, based on 142 cases of glioma. The authors reported no correlation between these 2 regions and survival. By extracting these 2 regions from our patient's deletion and comparing it to 12 other cases of 1p/19q codeletion oligodendrogliomas reported in the literature, we narrowed down the 14q loss possible critical region to 5.6 Mb mapping at 14q31.1q31.2. This region contains 2 potential relapse-related genes:SEL1LandSTON2.
机译:基于文献综述和我们的数据库,我们报告了在脑肿瘤中鉴定的最小的14Q缺失,其特征在于1P / 19Q Codeletion低级寡替氏菌瘤。 2013年,脑肿瘤的阵列比较基因组杂交揭示了1P / 19Q Comethion作为唯一的异常。 2019年,患者复发显示额外的异常,包括14季度删除16.5 MB,在14 Q24.2Q31.3。 该区域与2例先前鉴定的最小地区重叠,基于142例胶质瘤病例重叠。 作者报告了这两个地区与生存之间没有相关性。 通过从患者的缺失中提取这2个地区并将其与12例在文献中报告的1P / 19Q Codeletion oligodendrogliomas进行比较,我们将14Q亏损可能的关键区域缩小到14Q31.1Q31.2的5.6 MB映射。 该区域包含2个潜在的复发相关基因:Sel1landston2。

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