Pfaff Marie, Costa Philippos, Tang Haoyu, Sailo Bethsebie, Sharma Anup, Ahuja Nita
Department of Surgery, Yale School of Medicine, New Haven, CT 06520, USA.
Center for Surgical Science, Department of General, Visceral and Thoracic Surgery, Universitätsklinikum Hamburg Eppendorf, 20246 Hamburg, Germany.
Cancers (Basel). 2025 Aug 9;17(16):2610. doi: 10.3390/cancers17162610.
Uterine leiomyomas (ULM) and uterine leiomyosarcomas (ULMS) represent smooth muscle tumors with similar initial presentations but drastically different outcomes. This literature review analyzes the similarities and differences in their epigenetic profiles to identify diagnostic biomarkers and potential therapeutic targets that could improve clinical management. Both tumor types exhibit mostly distinct epigenetic signatures while sharing key pathway dysregulations. ULMS demonstrates global DNA hypomethylation, increased histone acetyltransferase activity, elevated Histone Deacetylase (HDAC) class I expression, and characteristic microRNA profiles. ULM displays focal methylation patterns and specific microRNA alterations that promote extracellular matrix accumulation. Despite these differences in epigenetic mechanisms, both tumors converge on dysregulation of signaling pathways including PI3K/AKT/mTOR, Wnt/β-catenin, and Transforming Growth Factor beta (TGF-β) signaling, suggesting common downstream effects from distinct epigenetic origins. Understanding the shared and distinct epigenetic landscape between ULM and ULMS will enhance our insights into tumor pathogenesis and may offer promising biomarkers and therapeutic targets.
子宫平滑肌瘤(ULM)和子宫平滑肌肉瘤(ULMS)是具有相似初始表现但预后截然不同的平滑肌肿瘤。这篇文献综述分析了它们表观遗传特征的异同,以确定可改善临床管理的诊断生物标志物和潜在治疗靶点。两种肿瘤类型大多表现出不同的表观遗传特征,同时存在关键信号通路的失调。ULMS表现出全基因组DNA低甲基化、组蛋白乙酰转移酶活性增加、I类组蛋白去乙酰化酶(HDAC)表达升高以及特征性的微小RNA谱。ULM呈现局部甲基化模式和促进细胞外基质积累的特定微小RNA改变。尽管表观遗传机制存在这些差异,但两种肿瘤在包括PI3K/AKT/mTOR、Wnt/β-连环蛋白和转化生长因子β(TGF-β)信号通路的失调上存在共同之处,这表明不同表观遗传起源具有共同的下游效应。了解ULM和ULMS之间共享和独特的表观遗传格局将增强我们对肿瘤发病机制的认识,并可能提供有前景的生物标志物和治疗靶点。