首页> 外文OA文献 >Loss of heterozygosity on chromosome 5q in ovarian cancer is frequently accompanied by TP53 mutation and identifies a tumour suppressor gene locus at 5q13.1-21.
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Loss of heterozygosity on chromosome 5q in ovarian cancer is frequently accompanied by TP53 mutation and identifies a tumour suppressor gene locus at 5q13.1-21.

机译:卵巢癌中5q染色体上杂合性的丧失经常伴有TP53突变,并鉴定了5q13.1-21处的抑癌基因基因座。

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摘要

Forty-nine ovarian tumours were examined for loss of heterozygosity (LOH) on chromosome 5 using eight microsatellite markers spanning both arms, including one at the APC locus. LOH on 5q was a frequent event, detectable in 23 of 49 (47%) tumours, whereas 5p LOH was detected in only 1 of 22 tumours (5%). Six tumours showed partial LOH on 5q, enabling the candidate region to be localised to a 22 cM region proximal to APC, flanked by D5S424 and D5S644. An association was found between 5q LOH and TP53 mutation, with 18 of 23 (78%) tumours with LOH on 5q also harbouring a TP53 mutation. LOH on 5q was observed in 6 of 18 (33%) stage I tumours, suggesting that it may be an early event in the molecular pathogenesis of certain ovarian carcinomas.
机译:使用横跨两臂的八个微卫星标记检查了49个卵巢肿瘤在5号染色体上的杂合性(LOH)丧失,其中一个位于APC位点。 5q的LOH是一个经常发生的事件,在49个肿瘤中的23个(47%)肿瘤中可以检测到,而在22个肿瘤中只有1个(5%)中检测到5p LOH。六个肿瘤在5q处显示局部LOH,使候选区域位于APC附近的22 cM区域,两侧为D5S424和D5S644。在5q LOH和TP53突变之间发现关联,在23个5q上具有LOH的肿瘤中,有18个(78%)也带有TP53突变。在18个I期肿瘤中,有6个(33%)的5q中观察到LOH,这表明这可能是某些卵巢癌分子发病机制的早期事件。

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