首页> 外文期刊>Modern Pathology >Identification of SYT-SSX transcripts from synovial sarcomas using RT-multiplex PCR and capillary electrophoresis
【24h】

Identification of SYT-SSX transcripts from synovial sarcomas using RT-multiplex PCR and capillary electrophoresis

机译:使用RT多重PCR和毛细管电泳从滑膜肉瘤中鉴定SYT-SSX转录本

获取原文
           

摘要

Synovial sarcomas are highly malignant tumors of soft tissue which are characterized by the t(X;18) resulting in SYT-SSX fusion transcript production. Diagnosis of these tumors based on histology can be challenging, particularly when minimal biopsy specimens are presented to the pathologist. Demonstration by molecular methods of SYT-SSX transcripts is a useful adjunct for diagnosis in these situations. We have developed an assay, which combines one-step RT-multiplex PCR with capillary electrophoresis to detect and genotype the SYT-SSX transcripts from synovial sarcomas. Small amplicons from chimeric transcripts as well as GAPD transcripts are differentially labeled with fluorophores, allowing detection and size discrimination by capillary electrophoresis. In a study of 32 formalin-fixed soft tissue tumor specimens, the assay detected chimeric transcripts from 17/22 (77%) synovial sarcomas. All five assay negative specimens yielded no intact RNA as evidenced by lack of a GAPD amplicon. Chimeric transcripts were not detected in 9/9 malignant peripheral nerve sheath tumors or 1/1 epithelioid sarcoma. Representative amplicons were sequenced and confirmed the genotype results obtained by capillary electrophoresis. One-step RT-multiplex PCR combined with capillary electrophoresis is a rapid and accurate method for the detection and genotypic classification of SYT-SSX transcripts from fixed tissue specimens.
机译:滑膜肉瘤是软组织的高度恶性肿瘤,其特征在于导致SYT-SSX融合转录产物产生的t(X; 18)。基于组织学对这些肿瘤的诊断可能具有挑战性,特别是当向病理学家提供最少的活检标本时。 SYT-SSX转录本的分子方法论证对于这些情况的诊断是有用的辅助手段。我们已经开发出一种检测方法,该方法将一步一步RT多重PCR与毛细管电泳相结合,以检测滑膜肉瘤的SYT-SSX转录本并进行基因分型。嵌合转录物和GAPD转录物的小扩增子用荧光团进行差异标记,可以通过毛细管电泳进行检测和大小区分。在对32个福尔马林固定的软组织肿瘤标本进行的研究中,该检测方法检测到来自17/22(77%)滑膜肉瘤的嵌合转录本。如缺少GAPD扩增子所证明的那样,所有五个化验阴性样本均未产生完整的RNA。在9/9恶性周围神经鞘瘤或1/1上皮样肉瘤中未检测到嵌合转录本。对代表性扩增子进行测序,并确认通过毛细管电泳获得的基因型结果。一步RT多重PCR与毛细管电泳相结合是一种快速,准确的方法,用于检测和固定组织标本中SYT-SSX转录本的基因型分类。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号