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Genome Wide Screening of CAG Trinucleotide Repeat Lengths in Breast Cancer

机译:乳腺癌CAG三核苷酸重复序列长度的基因组范围筛选

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摘要

Trinucleotide repeat sequences are widely present in the human genome. The expansion of CAG repeats have been studied very extensively, and shown to be the causative mechanism of more than 40 neuromuscular and neurodegenerative diseases. In the present study, we performed a genome wide screening of CAG repeat expansions in non-neoplastic tissues of 212 breast cancer cases and 196 healthy population controls using the Repeat Expansion Detection (RED) method. Distribution of CAG repeat lengths in cases was not significantly different from controls. However, dramatically expanded CAG repeats were detected in 2.4% (n = 5) of breast cancer cases where no repeats of similar size were detected in any of the healthy population controls. Although this trend shows only borderline significance (p = 0.06), this finding suggests a potential involvement of CAG repeat expansion in breast cancer susceptibility. These repeats may potentially affect the function of cancer predisposition genes, with a similar mechanism as in neurodegenerative and neuromuscular disorders.
机译:三核苷酸重复序列广泛存在于人类基因组中。对CAG重复序列的扩增已进行了广泛的研究,并被证明是40多种神经肌肉和神经退行性疾病的致病机制。在本研究中,我们使用重复扩展检测(RED)方法对212例乳腺癌病例和196个健康人群的非肿瘤组织中的CAG重复扩展进行了全基因组筛选。病例中CAG重复长度的分布与对照组无显着差异。但是,在2.4%(n = 5)的乳腺癌病例中检测到急剧扩大的CAG重复序列,在任何健康人群对照中均未检测到相似大小的重复序列。尽管这种趋势仅显示临界值(p = 0.06),但这一发现表明CAG重复扩增可能与乳腺癌易感性有关。这些重复可能潜在地影响癌症易感基因的功能,其机制与神经变性和神经肌肉疾病类似。

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