免疫组织化学
飞行1
免疫染色
融合基因
荧光原位杂交
肉瘤
促结缔组织增生性小圆细胞瘤
医学
尤因肉瘤
融合转录本
病理
聚合酶链反应
分子生物学
染色体易位
生物
基因
遗传学
染色体
作者
Victor Zota,Gene P. Siegal,David R. Kelly,Julia A. Bridge,Anders Berglund,Katherine Bui,Farah Khalil,Damon R. Reed,Soner Altiok,Anthony M. Magliocco,Marilyn M. Bui
标识
DOI:10.1080/15513815.2022.2117579
摘要
Background: Ewing sarcoma (ES) can be confirmed by identifying the EWSR1-FLI1 fusion transcript. This study is to investigate whether immunostaining (IHC) of PRKCB-a protein directly regulated by EWSR1-FLI1 is a surrogate maker for diagnosing ES in routine practice. Methods: Microarray gene expression analyses were conducted. RKCB IHC was applied to 69 ES confirmed by morphology and molecular methods, and 41 non-Ewing small round cell tumors. EWSR1 rearrangement, EWSR1-FLI1 fusion or t(11;22)(q24;q12) were identified by fluorescence in situ hybridization, reverse transcriptase polymerase chain reaction, or cytogenetic analysis, respectively. Results: Gene array analyses showed significant overexpression of the PRKCB in ES. PRKCB IHC was positive in 19 cases of ES with EWSR1-FLI1 fusion, 3 cases with cytogenetic 11:22 translocation and 59 cases with EWSR1 rearrangement while negative in only one EWSR1 rearranged case. PRKCB IHC is sensitive (98%) and specific (96%) in detecting EWSR1 rearranged ES. Conclusions: PRKCB is a reliable antibody for diagnosing ES in routine practice.
科研通智能强力驱动
Strongly Powered by AbleSci AI