Marrero-Gutiérrez Junier, Bueno Ana Carolina, Martins Clarissa Silva, Silva-Júnior Rui Milton Patrício, Dos Santos Antônio Carlos, Santos Marcelo Volpon, Wildemberg Luiz Eduardo, Antunes Ximene Lima da Silva, Gadelha Monica R, Moreira Ayrton Custodio, Vêncio Ricardo Zorzetto Nicoliello, Antonini Sonir Roberto R, de Castro Margaret
Department of Internal Medicine, Ribeirao Preto Medical School, University of São Paulo, Ribeirao Preto, Brazil.
Department of Pediatrics, Ribeirao Preto Medical School, University of São Paulo, Ribeirao Preto, Brazil.
Front Endocrinol (Lausanne). 2025 Jun 12;16:1585618. doi: 10.3389/fendo.2025.1585618. eCollection 2025.
Over the past decade, advancements in next-generation sequencing have significantly enhanced our understanding of the molecular pathogenesis of adamantinomatous craniopharyngiomas (ACP).
This study integrated methylome and transcriptome analyses in ACP samples to explore the potential interplay between DNA methylation and RNA expression signatures for diagnostic and prognostic applications in ACP patients.
This cross-sectional study evaluated clinicopathological features, DNA methylation, and gene expression profiles in 15 patients with ACP (33% women, age range: 3-55 years, 53% diagnosed before 18 years) treated at Ribeirao Preto Medical School, University of São Paulo.
Multidimensional scaling and principal component analysis identified two distinct clusters (ACP-A: n=9, ACP-B: n=6) with consistent composition across DNA methylation and gene expression profiles. While most clinical and histopathological characteristics were similar between clusters, ACP-A exhibited a longer median progression-free survival. ACP-B showed a higher prevalence of hypomethylated probes in CGI sites, and 63% of differentially methylated positions (DMPs) located in gene body regions. Differential methylation patterns were categorized into Methyl-Set1 (hypomethylated in ACP-A and hypermethylated in ACP-B) and Methyl-Set2 (hypermethylated in ACP-A and hypomethylated in ACP-B). Clustering analyses based on the methylation levels of probes and expression levels of the stringently filtered 212- and 37-gene sets further confirmed these two distinct ACP subgroups. Functional enrichment analysis highlighted key roles in synaptic modulation, nervous system development, cell adhesion, as well as pathways linked to RAS signaling, GTPase activity, and membrane potential regulation.
Although clinical characteristics were largely comparable between the clusters, ACP-B patients exhibited shorter median progression-free survival, suggesting a more aggressive phenotype. The higher prevalence of hypomethylation in ACP-B indicates increased transcriptional activation, potentially driving tumor aggressiveness. The strong concordance between methylation and transcriptomic data in the 212- and 37-gene sets underscores their potential as a clinically relevant molecular biomarker panel. These gene sets demonstrate robustness in distinguishing ACP clusters, making it a promising tool for clinical sample classification.
在过去十年中,下一代测序技术的进步显著增强了我们对造釉细胞瘤型颅咽管瘤(ACP)分子发病机制的理解。
本研究整合了ACP样本中的甲基化组和转录组分析,以探索DNA甲基化与RNA表达特征之间的潜在相互作用,用于ACP患者的诊断和预后应用。
这项横断面研究评估了圣保罗大学里贝朗普雷图医学院治疗的15例ACP患者(33%为女性,年龄范围:3 - 55岁,53%在18岁之前确诊)的临床病理特征、DNA甲基化和基因表达谱。
多维尺度分析和主成分分析确定了两个不同的聚类(ACP - A:n = 9,ACP - B:n = 6),其在DNA甲基化和基因表达谱中的组成一致。虽然聚类之间的大多数临床和组织病理学特征相似,但ACP - A的无进展生存期中位数更长。ACP - B在CGI位点的低甲基化探针患病率更高,且63%的差异甲基化位点(DMP)位于基因体区域。差异甲基化模式分为甲基化组1(在ACP - A中低甲基化,在ACP - B中高甲基化)和甲基化组2(在ACP - A中高甲基化,在ACP - B中低甲基化)。基于探针甲基化水平和严格筛选的212个和37个基因集的表达水平进行的聚类分析进一步证实了这两个不同的ACP亚组。功能富集分析突出了在突触调节、神经系统发育、细胞黏附以及与RAS信号传导、GTP酶活性和膜电位调节相关的途径中的关键作用。
虽然聚类之间的临床特征在很大程度上具有可比性,但ACP - B患者的无进展生存期中位数较短,表明其具有更具侵袭性的表型。ACP - B中低甲基化的较高患病率表明转录激活增加,可能驱动肿瘤侵袭性。212个和37个基因集中甲基化和转录组数据之间的强一致性强调了它们作为临床相关分子生物标志物面板的潜力。这些基因集在区分ACP聚类方面表现出稳健性,使其成为临床样本分类的有前途的工具。