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通过巢式逆转录聚合酶链反应检测尤因肉瘤家族石蜡包埋组织中的t(11;22)(q24;q12)易位断点

Detection of t(11;22)(q24;q12) translocation breakpoint in paraffin-embedded tissue of the Ewing's sarcoma family by nested reverse transcription-polymerase chain reaction.

作者信息

Adams V, Hany M A, Schmid M, Hassam S, Briner J, Niggli F K

机构信息

Department of Pathology, Institute of Clinical Pathology, Zürich, Switzerland.

出版信息

Diagn Mol Pathol. 1996 Jun;5(2):107-13. doi: 10.1097/00019606-199606000-00005.

DOI:10.1097/00019606-199606000-00005
PMID:8727097
Abstract

Tumors of the Ewing's sarcoma family often present a major diagnostic challenge for the pathologist. In recent years, significant progress has been made in identifying characteristic chromosomal rearrangements associated with certain solid tumors. More than 85% of Ewing's sarcoma and related tumors present a specific t(11;22) (q24;q12) balanced translocation, which generates a fusion transcript of the EWS gene and the FLI-1 gene. The cloning of the t(11;22)(q24;q12) breakpoint has raised the possibility of using a reverse transcription-polymerase chain reaction (RT-PCR) based assay as a diagnostic tool. We report an improvement of the established method, which currently depends on fresh or snap-frozen tissue, so that it is possible to use formalin-fixed, paraffin-embedded tissue as a source of RNA. The described nested RT-PCR assay enables the pathologist to investigate retrospectively archival tumor samples or to confirm the diagnosis in cases where no fresh or frozen material is available.

摘要

尤因肉瘤家族肿瘤常常给病理学家带来重大的诊断挑战。近年来,在识别与某些实体瘤相关的特征性染色体重排方面取得了显著进展。超过85%的尤因肉瘤及相关肿瘤呈现出特定的t(11;22)(q24;q12)平衡易位,这会产生EWS基因与FLI-1基因的融合转录本。t(11;22)(q24;q12)断点的克隆增加了将基于逆转录-聚合酶链反应(RT-PCR)的检测方法用作诊断工具的可能性。我们报告了对现有方法的改进,目前该方法依赖新鲜或速冻组织,改进后使得使用福尔马林固定、石蜡包埋组织作为RNA来源成为可能。所描述的巢式RT-PCR检测方法使病理学家能够回顾性研究存档的肿瘤样本,或在没有新鲜或冷冻材料的情况下确诊。

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