用比较基因组杂交检测少突胶质细胞肿瘤的染色体失衡

Violaine Bourdon , Ghislaine Plessis , Françoise Chapon , José Guarnieri , Jean Michel Derlon , Philippe Jonveaux
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引用次数: 11

摘要

采用比较基因组杂交(CGH)技术对7例分化良好的少突胶质细胞瘤、16例间变性少突胶质细胞瘤和2例少星形细胞瘤进行了研究。最常见的损失是在32%的病例中发现的1p和19q。在25%的间变性少突胶质细胞瘤的恶性进展过程中观察到9p的缺失。在两个间变性少突胶质细胞瘤中发现了1q的增益。16号和22号染色体的频繁丢失以前没有报道过。这些结果强调,CGH是一个强大的工具,胶质瘤的分类补充了传统的组织病理学方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Chromosome imbalances in oligodendroglial tumors detected by comparative genomic hybridization

Seven well-differentiated oligodendrogliomas, 16 anaplastic oligodendrogliomas and two cases of oligoastrocytomas were investigated by comparative genomic hybridization (CGH) on frozen tissue samples. The most frequent losses found involved 1p and 19q in 32% of cases. Loss of 9p was observed during malignant progression in 25% of anaplastic oligodendrogliomas. In two anaplastic oligodendrogliomas gain of 1q was found. The frequent losses of chromosome 16 and 22 have not been reported previously. These results underscore that CGH is a powerful tool for the classification of gliomas complementing the traditional histopathological approach.

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