SMARCA4型
卵黄囊
SMARCB1型
免疫组织化学
病理
绒毛膜癌
发病机制
医学
内淋巴囊
生物
解剖
胚胎
细胞生物学
基因表达
内耳
遗传学
染色质重塑
基因
作者
Costantino Ricci,Francesca Ambrosi,Tania Franceschini,Francesca Giunchi,Eugenia Franchini,Francesco Massari,Veronica Mollica,Federico Bianchi,Maurizio Colecchia,Andres Acosta,Michelangelo Fiorentino
标识
DOI:10.1016/j.prp.2022.154269
摘要
The recently described SWI/SNF complex-deficient sinonasal carcinoma (SMARCB1 & SMARCA4) may exhibit a yolk sac-like morphology. Tumors with similar features (yolk sac-like histology combined with the immunohistochemical loss of SMARCB1/INI1 and/or SMARCA4/BRG1) have also been described in other sites, such as the female genital tract. In this study, we immunohistochemically assessed SMARCB1/INI1 and SMARCA4/BRG1 expression to evaluate if these proteins could be involved in the pathogenesis of testicular yolk sac tumors of postpubertal type (YSTpt). Specifically, we analyzed a retrospective case series comprising pure YSTpt and mixed germ cell tumors of the testis (GCTT) with YSTpt components. In the present study, no testicular YSTpt showed loss of SMARCB1/INI1 (0/24, 0%) or SMARCA4/BRG1 (0/24, 0%). However, testicular choriocarcinoma (CHC) and isolated syncytiotrophoblast cells (iSTCs) demonstrated abnormal staining patterns for SMARCA4/BRG1 [CHC: 4/4 (100%); iSTCs: 12/12 (100%), respectively], including focal or diffuse loss of expression in a subset of cases. The results of our study suggest that functional loss of SMARCA4/BRG1 represents a recurrent event that may be relevant for the pathogenesis of a subset of testicular CHC.
科研通智能强力驱动
Strongly Powered by AbleSci AI