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A rare coincidence of different types of driver mutations among uterine leiomyomas (UL)

机译:子宫平滑肌中不同类型的司机突变的罕见巧合(UL)

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Mutations of mediator subcomplex 12 (MED12) and of high mobility group protein AT-hook 2 (HMGA2) are driver mutations in uterine leiomyomas (UL) that have not been observed to coexist in one tumor and even rarely coexist in different UL tumors of one patient. Here we describe a patient who underwent hysterectomy because of multiple leiomyomas which were studied by cytogenetics, MED12 hotspot sequencing, and copy number variation arrays. Two of the UL tumors had different HMGA2 rearrangements not detected by G-banding. Two UL tumors had deletions of the long arm of chromosome 3, in one case associated with a MED12 mutation. Both deletions lead to the loss of MED12L showing strong similarity with MED12. It remains to be determined if this gene can play a role in leiomyomagenesis independent of MED12. In summary, the patient presented exhibits an unusual coincidence of different driver mutations among her leiomyomas.
机译:介质子组合12(MED12)和高迁移率组蛋白的突变(HMGA2)的突变是尚未观察到在一个肿瘤中共存的子宫平滑肌瘤(UL)中的驾驶员突变,甚至很少在一个不同的UL肿瘤中共存病人。在这里,我们描述了由于细胞遗传学,Med12热点测序和拷贝数变化阵列进行了多种平滑肌瘤而接受子宫切除术的患者。 UL肿瘤中的两种具有不同的HMGA2重排未通过G型检测到。在与Med12突变相关的一种情况下,两个UL肿瘤缺少染色体3的长臂。两种缺失导致Med12L的丢失显示与Med12具有强烈相似之处。如果该基因可以在与Med12无关的Leiomyagenesis中发挥作用,则仍有待确定。总之,提出的患者展示了她的Leiomyomas之间不同驾驶员突变的不寻常吻合。

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