Sezer O, Jugovic D, Blohmer J U, Turzynski A, Thiel G, Langelotz C, Possinger K, Kovar H
Department of Oncology/Hematology, Institute of Medical Genetics Universitaetsklinikum Charité Medizinische Fakultaet der Humboldt-Universitaet Berlin, Germany.
Diagn Mol Pathol. 1999 Sep;8(3):120-4. doi: 10.1097/00019606-199909000-00003.
Rearrangements of the EWS gene with ETS transcription factor genes as a result of chromosomal translocation and high expression levels of CD99MIC2 characterize the Ewing family of tumors (EFT). This group of rather undifferentiated neoplasms affects bone and soft tissue in children and young adults mostly between 5 and 30 years of age (median, 15 years). This study reports a case of a CD99MIC2 positive small round cell tumor in the breast of a 60-year-old woman in whom a t(11;22)(q24;q12) chromosomal aberration was identified by cytogenetic analysis. Reverse transcriptase (RT)-polymerase chain reaction (PCR) followed by sequence analysis revealed expression of a chimera transcript in which EWS exon 10 was fused to FLI1 exon 6. Previously, this gene fusion has been reported to occur in approximately 3% of EFT. The specific gene rearrangement of EWS intron 10 was confirmed on Southern blot of genomic DNA. This study further contributes to the growing list of unusual neoplasms in adults that carry genotypic and phenotypic traits of the EFT.
由于染色体易位导致EWS基因与ETS转录因子基因重排以及CD99MIC2的高表达水平是尤因肿瘤家族(EFT)的特征。这组相当未分化的肿瘤主要影响5至30岁(中位年龄15岁)儿童和年轻成人的骨骼和软组织。本研究报告了一例60岁女性乳腺中CD99MIC2阳性的小圆细胞肿瘤病例,通过细胞遗传学分析鉴定出其存在t(11;22)(q24;q12)染色体畸变。逆转录(RT)-聚合酶链反应(PCR)及随后的序列分析显示出一种嵌合转录本的表达,其中EWS外显子10与FLI1外显子6融合。此前,据报道这种基因融合在约3%的EFT中出现。通过基因组DNA的Southern印迹证实了EWS内含子10的特异性基因重排。本研究进一步增加了携带EFT基因型和表型特征的成人罕见肿瘤的病例数。