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[分子生物学方法对骨与软组织肿瘤的病理诊断]

[Pathologic diagnosis on bone and soft tissue tumors by molecular biological methods].

作者信息

Nojima T, Takegami T, Abe S

机构信息

Department of Pathology, Kanazawa Medical University Hospital, Ishikawa.

出版信息

Rinsho Byori. 1997 Jul;45(7):661-6.

PMID:9256013
Abstract

Characteristic chromosome aberrations and the rearranged genes resulting in chimeric fusion genes have been reported in some bone and soft tissue tumors; t(X; 18) in synovial sarcoma, t(11; 22) in Ewing's sarcoma and primitive neuroectodermal tumor, and t(2; 13) in alveolar rhabdomyosarcoma. We practically used the chromosome analysis and the reverse transcription-polymerase chain reaction (PCR) method as a tool for diagnosis and follow up. All of 10 cases of synovial sarcoma had a chimeric product of SYT/SSX gene. Eleven cases of Ewing's sarcoma and primitive neuroectodermal tumor showed 6 variants of chimeric products between EWS gene and Fli1 gene in the PCR-directed sequence analysis. Although PAX3/FKHD or PAX7/FKHD transcripts were amplified in alveolar rhabdomyosarcoma cases, MyoD1 and myogenin gene which are myogenic transcription factor were also expressed in most rhabdomyosarcomas. These findings indicate that molecular biological analysis may be a useful supplementary method for pathologic diagnosis of bone and soft tissue tumors.

摘要

在一些骨和软组织肿瘤中已报道了特征性染色体畸变以及导致嵌合融合基因的重排基因;滑膜肉瘤中的t(X; 18)、尤因肉瘤和原始神经外胚层肿瘤中的t(11; 22),以及肺泡横纹肌肉瘤中的t(2; 13)。我们实际将染色体分析和逆转录聚合酶链反应(PCR)方法用作诊断和随访工具。10例滑膜肉瘤病例均有SYT/SSX基因的嵌合产物。在PCR定向序列分析中,11例尤因肉瘤和原始神经外胚层肿瘤显示了EWS基因和Fli1基因之间的6种嵌合产物变体。虽然在肺泡横纹肌肉瘤病例中扩增出了PAX3/FKHD或PAX7/FKHD转录本,但在大多数横纹肌肉瘤中也表达了作为肌源性转录因子的MyoD1和肌细胞生成素基因。这些发现表明分子生物学分析可能是骨和软组织肿瘤病理诊断的一种有用的辅助方法。

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