Resch Erin E, Makri Stavriani C, Ghanem Paola, Baraban Ezra G, Cohen Kenneth J, Cohen Alan R, Lipson Evan J, Pratilas Christine A
Division of Pediatric Oncology, Department of Oncology, The Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
NPJ Precis Oncol. 2025 Feb 21;9(1):48. doi: 10.1038/s41698-025-00826-8.
Enhancer of zeste homolog 2 (EZH2) is an essential epigenetic regulator of H3K27 histone methylation and is mutated or overexpressed in a wide variety of cancers. In melanoma, EZH2 overexpression contributes to excessive trimethylation of H3K27 on tumor suppressor genes and has been proposed to be a mechanism of tumor progression and metastasis. EZH2-targeted therapies have been successfully used to treat patients with follicular lymphoma and epithelioid sarcoma, but their clinical use in melanoma has not been described. Here, we describe a pediatric patient with multiply relapsed melanoma harboring an EZH2 A692V missense mutation, treated adjuvantly with the EZH2 inhibitor tazemetostat, who experienced a prolonged relapse-free survival.
zeste同源物2增强子(EZH2)是H3K27组蛋白甲基化的重要表观遗传调节因子,在多种癌症中发生突变或过表达。在黑色素瘤中,EZH2过表达导致肿瘤抑制基因上的H3K27过度三甲基化,被认为是肿瘤进展和转移的一种机制。EZH2靶向疗法已成功用于治疗滤泡性淋巴瘤和上皮样肉瘤患者,但其在黑色素瘤中的临床应用尚未见报道。在此,我们描述了一名患有多次复发黑色素瘤且携带EZH2 A692V错义突变的儿科患者,接受EZH2抑制剂他泽司他辅助治疗后,实现了长期无复发生存。