Epigenetic determinants in soft tissue sarcomas: molecular mechanisms and therapeutic targets.

IF 4.6 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Expert Opinion on Therapeutic Targets Pub Date : 2024-01-01 Epub Date: 2024-01-26 DOI:10.1080/14728222.2024.2306344
Alessandra Merlini, Martina Rabino, Silvia Brusco, Valeria Pavese, Debora Masci, Dario Sangiolo, Paolo Bironzo, Giorgio Vittorio Scagliotti, Silvia Novello, Lorenzo D'Ambrosio
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引用次数: 0

Abstract

Introduction: 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.

Areas covered: 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.

Expert opinion: 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.

软组织肉瘤中的表观遗传决定因素:分子机制和治疗目标。
导言:软组织肉瘤是一组罕见的间质肿瘤,其特点是晚期/转移期预后不良。人们对其分子决定因素的了解仍然相当有限。然而,近年来,表观遗传调控--在没有 DNA 序列变异的情况下改变基因表达/功能--已成为肉瘤成因和肉瘤进展的关键因素:在本文中,我们描述并回顾了参与染色质重塑的主要表观遗传学机制及其在不同软组织肉瘤组织类型中作为疾病驱动因素的作用,重点关注上皮样肉瘤、滑膜肉瘤和恶性周围神经鞘瘤。我们以染色质重塑复合物为重点,深入探讨了 BAF 复合物改变在这些软组织肉瘤组织类型中的作用。同时,我们还强调了利用软组织肉瘤表观遗传失调开发合理、创新治疗方法的当前先进水平和未来前景:迄今为止,转移性/晚期肉瘤的治疗方案非常有限,主要以细胞毒药物为主,而且效果一般。在不断尝试寻找新靶点和创新有效药物的过程中,表观遗传学机制是一个新兴且前景广阔的研究领域,尤其是针对恶性周围神经鞘瘤、上皮样肉瘤和滑膜肉瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
8.90
自引率
1.70%
发文量
58
审稿时长
3 months
期刊介绍: The journal evaluates molecules, signalling pathways, receptors and other therapeutic targets and their potential as candidates for drug development. Articles in this journal focus on the molecular level and early preclinical studies. Articles should not include clinical information including specific drugs and clinical trials. The Editors welcome: Reviews covering novel disease targets at the molecular level and information on early preclinical studies and their implications for future drug development. Articles should not include clinical information including specific drugs and clinical trials. Original research papers reporting results of target selection and validation studies and basic mechanism of action studies for investigative and marketed drugs. The audience consists of scientists, managers and decision makers in the pharmaceutical industry, academic researchers working in the field of molecular medicine and others closely involved in R&D.
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