Katayama Yoshihiro, Iwasaki Takeshi, Yamamoto Takeo, Shimada Naomi, Nakashima Miya, Toya Masato, Narutomi Fumiya, Tomonaga Takumi, Kato Kiyoko, Oda Yoshinao
Department of Anatomic Pathology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Departments of Gynecology and Obstetrics, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Cancer Sci. 2025 Mar;116(3):835-845. doi: 10.1111/cas.16423. Epub 2024 Dec 23.
Ovarian carcinosarcoma (OCS) is a rare and aggressive tumor, and the development of its sarcomatous component is believed to be due to epithelial-mesenchymal transition (EMT). The SWIch/sucrose nonfermentable chromatin remodeling factor (CRF) is closely related to EMT; however, the relationship between CRF and EMT in OCS remains unclear. In this study, we analyzed the protein expression of CRFs, including ARID1A and SMARCA4, and their downstream mRNA expression in 28 OCS cases, two fallopian tube CS cases, and one peritoneal CS case. ARID1A and SMARCA4 exhibited a histological type-specific loss of protein expression in 5 of 11 (45%) endometrioid cases and all 5 serous/homologous OCS cases, respectively. The mRNA analysis suggested that sarcomatogenesis is induced by the transforming growth factor-β and Hippo signaling pathways, both of which regulate YAP1. Immunostaining for YAP1 suggested YAP1-associated sarcomatogenesis in the CRF-retained group, whereas YAP1-unassociated sarcomatogenesis was suggested in the CRF-reduced group. High-grade serous carcinoma cell line experiments showed that the transcriptome of the SMARCA4-knockdown group showed lower expression of the epithelial gene CDH1 and higher expression of mesenchymal genes such as VIM, ZEB1, and SNAI1 than the control group. Moreover, cell adhesion disappeared and cell morphology changed to a spindle shape, indicating sarcomatogenesis. In conclusion, this study reveals a mechanism for sarcoma development in OCS and provides novel therapeutic possibilities.
卵巢癌肉瘤(OCS)是一种罕见且侵袭性强的肿瘤,其肉瘤成分的发生被认为是由于上皮-间质转化(EMT)。SWI/SNF染色质重塑因子(CRF)与EMT密切相关;然而,CRF与OCS中EMT的关系仍不清楚。在本研究中,我们分析了28例OCS病例、2例输卵管癌肉瘤病例和1例腹膜癌肉瘤病例中CRF(包括ARID1A和SMARCA4)的蛋白表达及其下游mRNA表达。在11例子宫内膜样病例中的5例(45%)以及所有5例浆液性/同源性OCS病例中,ARID1A和SMARCA4分别表现出组织学类型特异性的蛋白表达缺失。mRNA分析表明,肉瘤发生是由转化生长因子-β和Hippo信号通路诱导的,这两条通路均调节YAP1。YAP1免疫染色表明,在CRF保留组中存在与YAP1相关的肉瘤发生,而在CRF减少组中提示存在与YAP1无关的肉瘤发生。高级别浆液性癌细胞系实验表明,与对照组相比,SMARCA4敲低组的转录组显示上皮基因CDH1表达降低,间充质基因如VIM、ZEB1和SNAI1表达升高。此外,细胞黏附消失,细胞形态变为纺锤形,表明发生了肉瘤变。总之,本研究揭示了OCS中肉瘤发生的机制,并提供了新的治疗可能性。