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TaqMan连接探针与逆转录聚合酶链反应:肺泡横纹肌肉瘤、滑膜肉瘤及促纤维增生性小圆细胞肿瘤的检测

TaqMan junction probes and the reverse transcriptase polymerase chain reaction: detection of alveolar rhabdomyosarcoma, synovial sarcoma, and desmoplastic small round cell tumor.

作者信息

Cummings Thomas J, Brown Nicholas M, Stenzel Timothy T

机构信息

Department of Pathology, Duke University Medical Center, Durham, North Carolina 27710, USA.

出版信息

Ann Clin Lab Sci. 2002 Summer;32(3):219-24.

Abstract

The reverse transcriptase polymerase chain reaction (RT-PCR) provides a technique to diagnose a group of sarcomas and small round cell tumors that contain specific chromosomal translocations and chimeric gene fusion products. We adapted real-time qualitative RT-PCR to utilize dual-labeled, fluorogenic, TaqMan probes, which hybridize to targets that overlap the junction of the chimeric gene fusions in alveolar rhabdomyosarcoma (ARMS), synovial sarcoma (SS), and desmoplastic small round cell tumor (DSRCT). Assays were confirmed on cell lines and tissue samples; appropriate negative amplification assays were obtained when each tumor-specific probe and primer set was used on different neoplasms and cell lines that were not expected to harbor the specific translocations and chimeric gene fusions. Although our cases are few, we speculate that as more molecular variants of ARMS, SS, and DSRCT are discovered, clinical correlations based on precise molecular features will be required and fusion site specificity will be assured by the use of junction-based TaqMan probes.

摘要

逆转录聚合酶链反应(RT-PCR)提供了一种技术,用于诊断一组含有特定染色体易位和嵌合基因融合产物的肉瘤和小圆细胞肿瘤。我们采用实时定性RT-PCR,利用双标记、荧光TaqMan探针,这些探针与肺泡横纹肌肉瘤(ARMS)、滑膜肉瘤(SS)和促纤维增生性小圆细胞肿瘤(DSRCT)中嵌合基因融合连接处重叠的靶标杂交。在细胞系和组织样本上对检测方法进行了验证;当在预期不含有特定易位和嵌合基因融合的不同肿瘤和细胞系上使用每种肿瘤特异性探针和引物组时,获得了适当的阴性扩增检测结果。尽管我们的病例数量较少,但我们推测,随着ARMS、SS和DSRCT的更多分子变体被发现,将需要基于精确分子特征的临床相关性,并且通过使用基于连接点的TaqMan探针将确保融合位点特异性。

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