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BRCA1 methylation and BRCA1 mutations in ovarian cancer.

机译:卵巢癌中的BRCA1甲基化和BRCA1突变。

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摘要

With great interest we have read the much needed re-appraisal of BRCAl methylation studies in ovarian cancer [1]. The authors noted that differences in experimental methods resulted in a broad range of BRCAl methylation, between 5% and 40%. Indeed, Suijkerbuijk et al. [2] found a high discrepancy between methylation-spedfic PCR (MSP) and quantitative multiplex MSP (QM-MSP) in the same samples. However, two unrelated quantitative methods, QM-MSP and methylation-specific multiplex ligation-dependent probe amplification (MS-MLPA), correlated strongly.
机译:我们非常感兴趣地阅读了在卵巢癌中急需的BRCA1甲基化研究的重新评估[1]。作者指出,实验方法的差异导致BRCAl甲基化的范围很广,介于5%和40%之间。确实,Suijkerbuijk等人。 [2]在相同样品中发现甲基化专一性PCR(MSP)与定量多重MSP(QM-MSP)之间存在高度差异。但是,两种不相关的定量方法,即QM-MSP和甲基化特异性多重连接依赖探针扩增(MS-MLPA),密切相关。

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