{"title":"CBX4是滑膜肉瘤中SS18::SSX的一种新型相互作用因子。","authors":"Ainiah Rushdiana Raquib, Torsten O Nielsen","doi":"10.1016/j.labinv.2025.104243","DOIUrl":null,"url":null,"abstract":"<p><p>Synovial sarcoma is an aggressive cancer generally affecting adolescents and young adults, and is characterized by high rates of recurrence and metastasis. It is primarily driven by the fusion oncoprotein SS18::SSX, the product of a pathognomonic chromosomal translocation t(X;18), which facilitates widespread epigenetic dysregulation through interactions with complexes such as the BAF complex and polycomb repressive complexes. Previous attempts to perform mass spectrometry of the SS18::SSX interactome has been limited by the lack of an antibody to detect the endogenous protein, hence relying on single cell lines with exogenous tags. We previously used a monoclonal antibody which specifically detects SS18::SSX containing the canonical fusion junction (seen in 95% of cases) and established its utility in several applications. Using that antibody, mass spectrometry analysis revealed that the SS18::SSX protein undergoes alternative splicing of exon 8 in SS18. We next performed immunoprecipitation mass spectrometry of SS18::SSX in six immortalized human synovial sarcoma cell lines and identified the canonical polycomb repressive complex member chromobox 4, CBX4, as a novel interactor of the oncoprotein. Immunohistochemical staining of several epigenetic factors on a human synovial sarcoma tissue microarray showed association of synovial sarcoma samples with higher CBX4 expression. Lastly, analysis of CBX4 expression across 337 samples from 12 sarcoma subtypes, carcinomas and normal tissue demonstrates higher expression in synovial sarcoma samples as compared to other tissue types. These results highlight a crucial approach in identifying important partners of SS18::SSX in synovial sarcoma to establish new biological pathways that contribute to the disease.</p>","PeriodicalId":17930,"journal":{"name":"Laboratory Investigation","volume":" ","pages":"104243"},"PeriodicalIF":4.2000,"publicationDate":"2025-09-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"CBX4 is a novel interactor of SS18::SSX in synovial sarcoma.\",\"authors\":\"Ainiah Rushdiana Raquib, Torsten O Nielsen\",\"doi\":\"10.1016/j.labinv.2025.104243\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Synovial sarcoma is an aggressive cancer generally affecting adolescents and young adults, and is characterized by high rates of recurrence and metastasis. It is primarily driven by the fusion oncoprotein SS18::SSX, the product of a pathognomonic chromosomal translocation t(X;18), which facilitates widespread epigenetic dysregulation through interactions with complexes such as the BAF complex and polycomb repressive complexes. Previous attempts to perform mass spectrometry of the SS18::SSX interactome has been limited by the lack of an antibody to detect the endogenous protein, hence relying on single cell lines with exogenous tags. We previously used a monoclonal antibody which specifically detects SS18::SSX containing the canonical fusion junction (seen in 95% of cases) and established its utility in several applications. Using that antibody, mass spectrometry analysis revealed that the SS18::SSX protein undergoes alternative splicing of exon 8 in SS18. We next performed immunoprecipitation mass spectrometry of SS18::SSX in six immortalized human synovial sarcoma cell lines and identified the canonical polycomb repressive complex member chromobox 4, CBX4, as a novel interactor of the oncoprotein. Immunohistochemical staining of several epigenetic factors on a human synovial sarcoma tissue microarray showed association of synovial sarcoma samples with higher CBX4 expression. Lastly, analysis of CBX4 expression across 337 samples from 12 sarcoma subtypes, carcinomas and normal tissue demonstrates higher expression in synovial sarcoma samples as compared to other tissue types. These results highlight a crucial approach in identifying important partners of SS18::SSX in synovial sarcoma to establish new biological pathways that contribute to the disease.</p>\",\"PeriodicalId\":17930,\"journal\":{\"name\":\"Laboratory Investigation\",\"volume\":\" \",\"pages\":\"104243\"},\"PeriodicalIF\":4.2000,\"publicationDate\":\"2025-09-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Laboratory Investigation\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1016/j.labinv.2025.104243\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MEDICINE, RESEARCH & EXPERIMENTAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Laboratory Investigation","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.labinv.2025.104243","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MEDICINE, RESEARCH & EXPERIMENTAL","Score":null,"Total":0}
CBX4 is a novel interactor of SS18::SSX in synovial sarcoma.
Synovial sarcoma is an aggressive cancer generally affecting adolescents and young adults, and is characterized by high rates of recurrence and metastasis. It is primarily driven by the fusion oncoprotein SS18::SSX, the product of a pathognomonic chromosomal translocation t(X;18), which facilitates widespread epigenetic dysregulation through interactions with complexes such as the BAF complex and polycomb repressive complexes. Previous attempts to perform mass spectrometry of the SS18::SSX interactome has been limited by the lack of an antibody to detect the endogenous protein, hence relying on single cell lines with exogenous tags. We previously used a monoclonal antibody which specifically detects SS18::SSX containing the canonical fusion junction (seen in 95% of cases) and established its utility in several applications. Using that antibody, mass spectrometry analysis revealed that the SS18::SSX protein undergoes alternative splicing of exon 8 in SS18. We next performed immunoprecipitation mass spectrometry of SS18::SSX in six immortalized human synovial sarcoma cell lines and identified the canonical polycomb repressive complex member chromobox 4, CBX4, as a novel interactor of the oncoprotein. Immunohistochemical staining of several epigenetic factors on a human synovial sarcoma tissue microarray showed association of synovial sarcoma samples with higher CBX4 expression. Lastly, analysis of CBX4 expression across 337 samples from 12 sarcoma subtypes, carcinomas and normal tissue demonstrates higher expression in synovial sarcoma samples as compared to other tissue types. These results highlight a crucial approach in identifying important partners of SS18::SSX in synovial sarcoma to establish new biological pathways that contribute to the disease.
期刊介绍:
Laboratory Investigation is an international journal owned by the United States and Canadian Academy of Pathology. Laboratory Investigation offers prompt publication of high-quality original research in all biomedical disciplines relating to the understanding of human disease and the application of new methods to the diagnosis of disease. Both human and experimental studies are welcome.