Fusion of the Genes PHF1 and TFE3 in Malignant Chondroid Syringoma

被引:23
作者
Panagopoulos, Ioannis [1 ]
Gorunova, Ludmila [1 ]
Lund-Iversen, Marius [2 ]
Bassarova, Assia [2 ]
Heim, Sverre [1 ,3 ]
机构
[1] Oslo Univ Hosp, Norwegian Radium Hosp, Inst Canc Genet & Informat, Sect Canc Cytogenet, POB 4954 Nydalen, NO-0424 Oslo, Norway
[2] Oslo Univ Hosp, Dept Pathol, Oslo, Norway
[3] Univ Oslo, Fac Med, Inst Clin Med, Oslo, Norway
关键词
Malignant chondroid syringoma; PHF1; TFE3; PHF1-TFE3 fusion gene; RNA sequencing; SOFT PART SARCOMA; CUTANEOUS MYOEPITHELIOMA; TISSUE; TUMOR; TRANSLOCATION; TRANSCRIPTION; REARRANGEMENT; NEOPLASMS; IDENTIFICATION; DEFINES;
D O I
10.21873/cgp.20139
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background/Aim: Malignant chondroid syringoma is a rare tumor of unknown pathogenesis. Materials and Methods: Genetic analyses were performed on a malignant chondroid syringoma. Results: G-banding analysis of short-term cultured tumor cells yielded the karyotype 46,Y,t(X;6)(p11;p21)[15]/46,XY[2]. RNA sequencing detected an in-frame fusion of PHF1 from 6p21 with TFE3 from Xp11, verified by RT-PCR and Sanger sequencing. Genomic PCR showed that the PHF1-TFE3 junction was identical to the fusion found by RNA sequencing and RT-PCR. Conclusion: Malignant chondroid syringoma is genetically related to tumors with PHF1 rearrangements such as low-grade endometrial sarcoma and ossifying fibromyxoid tumor, but also with tumors having TFE3 rearrangements such as renal cell carcinoma, alveolar soft part sarcoma, PEComa, and epithelioid hemangioendothelioma. Further investigations on malignant chondroid syringomas are needed in order to determine whether genetic heterogeneity exists among them and the clinical impact of the PHF1-TFE3 fusion.
引用
收藏
页码:345 / 351
页数:7
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