Hasegawa Nobuhiko, Benabdallah Nezha S, Smith-Fry Kyllie, Li Li, McCollum Sarah, Li Jinxiu, Jones Caelen A, Wagner Lena, Dalal Vineet, Golde Viola, Pejkovska Anastasija, Carroll Lara, Haldar Malay, Pollack Seth M, Lowe Scott W, Nielsen Torsten O, Banito Ana, Jones Kevin B
Department of Orthopaedics.
Department of Oncological Sciences.
J Clin Invest. 2025 Apr 29;135(13). doi: 10.1172/JCI190855. eCollection 2025 Jul 1.
Synovial sarcoma is an aggressive soft-tissue cancer driven by the chimeric SS18::SSX fusion oncoprotein, which disrupts chromatin remodeling by combining two antagonistic transcriptional regulators. SS18 participates in BAF complexes that open chromatin, while the SSX genes are cancer-testis antigens that interface with chromatin decorated with monoubiquitinated histone H2A placed by polycomb repressive complex activity. Because KDM2B brings polycomb repressive complex to unmethylated CpG islands, it is plausible that methylation directly determines the distribution of SS18::SSX to target loci. Given that synovial sarcoma is also characterized by a peculiarly low DNA hypomethylation profile, we hypothesized that further disturbance of DNA methylation would have a negative impact on synovial sarcoma growth. DNMT1 disruption by CRISPR/Cas9 targeting or pharmacological inhibition with cytidine analogs 5-aza-2'-deoxycytidine (decitabine) and 5-azacytidine led to decreased genome-wide methylation, redistribution of SS18::SSX, and altered gene expression profiles, most prominently including upregulation of tumor suppressor genes, immune-related genes, and mesenchymal differentiation-related genes. These drugs suppressed growth of synovial sarcoma cell lines and drove cytoreduction in mouse genetic models. DNMT1 inhibitors, already approved for treating myelodysplastic syndromes, warrant further clinical investigation for synovial sarcoma as repurposed, targeted treatments exploiting a vulnerability in the intrinsic biology of this cancer.
滑膜肉瘤是一种侵袭性软组织癌,由嵌合的SS18::SSX融合癌蛋白驱动,该蛋白通过结合两种拮抗转录调节因子破坏染色质重塑。SS18参与打开染色质的BAF复合物,而SSX基因是癌睾丸抗原,与通过多梳抑制复合物活性放置单泛素化组蛋白H2A修饰的染色质相互作用。由于KDM2B将多梳抑制复合物带到未甲基化的CpG岛,甲基化直接决定SS18::SSX在靶位点的分布是合理的。鉴于滑膜肉瘤的特征还在于DNA低甲基化程度特别低,我们假设DNA甲基化的进一步紊乱会对滑膜肉瘤的生长产生负面影响。通过CRISPR/Cas9靶向或用胞苷类似物5-氮杂-2'-脱氧胞苷(地西他滨)和5-氮杂胞苷进行药理抑制来破坏DNMT1,导致全基因组甲基化降低、SS18::SSX重新分布以及基因表达谱改变,最显著的是包括肿瘤抑制基因、免疫相关基因和间充质分化相关基因的上调。这些药物抑制了滑膜肉瘤细胞系的生长,并在小鼠遗传模型中促进了细胞减少。DNMT1抑制剂已被批准用于治疗骨髓增生异常综合征,作为利用这种癌症内在生物学弱点的重新利用的靶向治疗方法,对滑膜肉瘤进行进一步的临床研究是有必要的。