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Low frequency of somatic mutations in the FH/multiple cutaneous leiomyomatosis gene in sporadic leiomyosarcomas and uterine leiomyomas

机译:散发性平滑肌肉瘤和子宫平滑肌瘤的FH /多发性皮肤平滑肌瘤基因中的体细胞突变频率较低

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摘要

Germline mutations in the fumarate hydratase gene at 1q43 predispose to dominantly inherited skin and uterine leiomyomata and leiomyosarcomas. The enzyme, which is a component of the tricarboxylic acid cycle, acts as a tumour suppressor. To evaluate fumarate hydratase in respective sporadic tumours, we analysed a series of 26 leiomyosarcomas and 129 uterine leiomyomas (from 21 patients) for somatic mutations in fumarate hydratase and allelic imbalance around 1q43. None of the 26 leiomyosarcomas harboured somatic mutations in fumarate hydratase. Fifty per cent of leiomysarcomas tested showed evidence of allelic imbalance at 1q, but this was not confined to the vicinity of fumarate hydratase. Only 5% (seven out of 129) of the leiomyomas showed allele imbalance at 1q42-q43 and no somatic mutations in fumarate hydratase were observed. Our findings indicate that mutations in fumarate hydratase do not play a major role in the development of sporadic leiomyosarcomas or uterine leiomyomas.
机译:1q43富马酸酯水合酶基因中的种系突变易导致显性遗传的皮肤和子宫平滑肌瘤和平滑肌肉瘤。该酶是三羧酸循环的组成部分,起着抑癌作用。为了评估各个散发性肿瘤中的富马酸水合酶,我们分析了一系列26例平滑肌肉瘤和129例子宫平滑肌瘤(来自21例患者)的富马酸水合酶的体细胞突变和等位基因在1q43附近的失衡。 26个平滑肌肉瘤中没有一个具有富马酸盐水合酶的体细胞突变。测试的平滑肌肉瘤中有50%在1q时显示等位基因失衡的证据,但这并不限于富马酸盐水合酶附近。仅有5%(129例中有7例)平滑肌瘤在1q42-q43处显示等位基因失衡,未观察到富马酸酯水合酶的体细胞突变。我们的发现表明,富马酸盐水合酶的突变在散发性平滑肌肉瘤或子宫平滑肌瘤的发生中不发挥主要作用。

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