首页> 外文期刊>Brain pathology >Multiplex ligation-dependent probe amplification for the detection of 1p and 19q chromosomal loss in oligodendroglial tumors.
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Multiplex ligation-dependent probe amplification for the detection of 1p and 19q chromosomal loss in oligodendroglial tumors.

机译:多重连接依赖探针扩增可检测少突胶质细胞瘤中的1p和19q染色体缺失。

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摘要

Multiplex ligation-dependent probe amplification (MLPA) is a new assay for the detection of multiple chromosomal deletions in tumor tissue in a single experiment. Since genotyping of gliomas with oligodendroglial features by the detection of 1p/19q chromosomal deletions became essential for treatment decisions, we developed and validated an MLPA-based assay to determine these losses in formalin fixed and paraffin embedded oligodendroglial tumors (OG). Nineteen OGs, and 10 control samples were analyzed by MLPA and the results were correlated with those obtained by fluorescent in situ hybridization (FISH). The MLPA results were reproducible in all samples in which repeated experiments were performed. In 18 of 19 OGs, MLPA and FISH were concordant for presence or absence of 1p deletion. In 3 OGs, MLPA detected a 19q deletion not shown by FISH. For the other 15 OGs, MLPA and FISH were concordant. In one sample with 50% to 75% of tumor, MLPA failed to detect the 1p/19q deletions revealed by FISH (though with borderline values of significance). We conclude that MLPA is a valid and reproducible method for the detection of 1p/19q chromosomal deletions in OGs stored on formalin fixed, paraffin embedded tissue.
机译:多重连接依赖性探针扩增(MLPA)是一项用于在单个实验中检测肿瘤组织中多个染色体缺失的新方法。由于通过检测1p / 19q染色体缺失来对具有少突胶质细胞特征的神经胶质瘤进行基因分型对于治疗决策至关重要,因此我们开发并验证了基于MLPA的测定方法,以确定在福尔马林固定和石蜡包埋的少突胶质细胞瘤(OG)中的这些损失。 MLPA分析了19个OG和10个对照样品,结果与通过荧光原位杂交(FISH)获得的结果相关。在执行重复实验的所有样品中,MLPA结果均具有可重复性。在19个OG中的18个中,MLPA和FISH对1p缺失的存在与否是一致的。在3个OG中,MLPA检测到FISH未显示的19q缺失。对于其他15个OG,MLPA和FISH是一致的。在一个肿瘤占50%至75%的样本中,MLPA无法检测到FISH揭示的1p / 19q缺失(尽管具有显着的临界值)。我们得出的结论是,MLPA是用于检测存储在福尔马林固定的石蜡包埋组织中的OG中1p / 19q染色体缺失的有效且可重复的方法。

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