上皮样肉瘤
滑膜肉瘤
表观遗传学
肉瘤
周围神经鞘恶性肿瘤
癌症研究
软组织肉瘤
染色质
DNA甲基化
软组织
生物
染色质重塑
医学
生物信息学
病理
基因
遗传学
基因表达
免疫组织化学
作者
Alessandra Merlini,Martina Rabino,Silvia Brusco,Valeria Pavese,Debora Masci,Dario Sangiolo,Paolo Bironzo,Giorgio V. Scagliotti,Silvia Novello,Lorenzo D’Ambrosio
标识
DOI:10.1080/14728222.2024.2306344
摘要
Soft tissue sarcomas are a group of rare, mesenchymal tumors characterized by dismal prognosis in advanced/metastatic stages. Knowledge of their molecular determinants is still rather limited. However, in recent years, epigenetic regulation - the modification of gene expression/function without DNA sequence variation - has emerged as a key player both in sarcomagenesis and sarcoma progression.Herein, we describe and review the main epigenetic mechanisms involved in chromatin remodeling and their role as disease drivers in different soft tissue sarcoma histotypes, focusing on epithelioid sarcoma, synovial sarcoma, and malignant peripheral nerve sheath tumors. Focusing on chromatin-remodeling complexes, we provide an in-depth on the role of BAF complex alterations in these soft tissue sarcoma histotypes. In parallel, we highlight current state-of-the-art and future perspectives in the development of rational, innovative treatments leveraging on epigenetic dysregulation in soft tissue sarcomas.Therapeutic options for metastatic/advanced sarcomas are to date very limited and largely represented by cytotoxic agents, with only modest results. In the continuous attempt to find novel targets and innovative, effective drugs, epigenetic mechanisms represent an emerging and promising field of research, especially for malignant peripheral nerve sheath tumors, epithelioid and synovial sarcoma.
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