首页> 外文期刊>The Journal of molecular diagnostics: JMD >JAZF1/JJAZ1 gene fusion in endometrial stromal sarcomas: molecular analysis by reverse transcriptase-polymerase chain reaction optimized for paraffin-embedded tissue.
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JAZF1/JJAZ1 gene fusion in endometrial stromal sarcomas: molecular analysis by reverse transcriptase-polymerase chain reaction optimized for paraffin-embedded tissue.

机译:JAZF1 / JJAZ1基因融合在子宫内膜间质肉瘤:分子分析,通过逆转录酶-聚合酶链反应优化石蜡包埋的组织。

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摘要

Endometrial stromal tumors are rare uterine neoplasms including benign stromal nodules, low-grade endometrial stromal sarcomas (ESS), and undifferentiated endometrial sarcomas (UES), the latter representing the most aggressive form. Morphological characteristics and cytogenetic abnormalities are heterogeneous, making diagnosis difficult. Recently, a gene fusion on chromosome 7 that includes two zinc-finger genes (JAZF1 and JJAZ1) has been discovered in these tumors. Hitherto only 31 cases, described by three different research groups, have shown JAZF1/JJAZ1 fusion in approximately 50% of all analyzed low-grade ESSs whereas it is less frequent in UESs. In this study we analyzed 20 ESS and 2 UES cases using two-step reverse transcriptase-polymerase chain reaction optimized for formalin-fixed, paraffin-embedded tissue. In our subset of samples, the JAZF1/JJAZ1 fusion transcript occurred in 80% of analyzed ESS cases and in none of two UES cases. In comparison to published data, our results identified the JAZF1/JJAZ1 gene fusion more frequently in endometrial stromal tumors than hitherto presumed. This cytogenetic abnormality was not present in normal endometria, leiomyomas, or leiomyosarcomas or in lung, gastric, or hepatic carcinomas, indicating its specificity for endometrial stromal tumors. In combination with other established methods, accurate reverse transcriptase-polymerase chain reaction analysis of JAZF1/JJAZ1 gene fusion may be useful in diagnosing difficult or unusual ESS/UES cases.
机译:子宫内膜间质瘤是罕见的子宫肿瘤,包括良性间质结节,低度子宫内膜间质肉瘤(ESS)和未分化的子宫内膜肉瘤(UES),后者代表最具侵袭性的形式。形态特征和细胞遗传学异常是异质的,使得诊断困难。最近,在这些肿瘤中发现了7号染色体上的基因融合体,其中包括两个锌指基因(JAZF1和JJAZ1)。迄今为止,由三个不同的研究小组描述的仅31例病例在所有分析的低级ESS中约有50%显示出JAZF1 / JJAZ1融合,而在UES中则较少。在这项研究中,我们使用针对福尔马林固定,石蜡包埋的组织进行了优化的两步逆转录酶-聚合酶链反应分析了20例ESS和2例UES病例。在我们的样本子集中,在分析的ESS病例中有80%发生了JAZF1 / JJAZ1融合转录本,而在两个UES病例中均未发生。与已发表的数据相比,我们的结果发现子宫内膜间质瘤中的JAZF1 / JJAZ1基因融合比迄今推测的更为频繁。这种细胞遗传学异常在正常子宫内膜,平滑肌瘤或平滑肌肉瘤或肺,胃或肝癌中不存在,表明其对子宫内膜间质瘤的特异性。与其他已建立的方法结合,对JAZF1 / JJAZ1基因融合的准确逆转录酶-聚合酶链反应分析可能有助于诊断困难或异常的ESS / UES病例。

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