Department of Pediatrics, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.
Department of Genetics, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.
Pediatr Blood Cancer. 2022 Jul;69(7):e29553. doi: 10.1002/pbc.29553. Epub 2021 Dec 31.
Pediatric adrenocortical tumors (ACT) are rare aggressive neoplasms with heterogeneous prognosis. Despite extensive efforts, identifying reliable prognostic factors for pediatric patients with ACT remains a challenge. MicroRNA (miRNA) signatures have been associated with cancer diagnosis, treatment response, and prognosis of several types of cancer. However, the role of miRNAs has been poorly explored in pediatric ACT. In this study, we performed miRNA microarray profiling on a cohort of 37 pediatric ACT and nine nonneoplastic adrenal (NNA) samples and evaluated the prognostic significance of abnormally expressed miRNAs using Kaplan-Meier plots, log-rank test, and Cox regression analysis. We identified a total of 98 abnormally expressed miRNAs; their expression profile discriminated ACT from NNAs. Among the 98 deregulated miRNAs, 17 presented significant associations with patients' survival. In addition, higher expression levels of hsa-miR-630, -139-3p, -125a-3p, -574-5p, -596, -564, -1321, and -423-5p and lower expression levels of hsa-miR-377-3p, -126-3p, -410, -136-3p, -29b-3p, -29a-3p, -337-5p, -143-3p, and 140-5p were significantly associated with poor prognosis, tumor relapse, and/or death. Importantly, the expression profile of these 17 miRNAs stratified patients into two groups of ACTs with different clinical outcomes. Although some individual miRNAs exhibit potential prognostic values in ACTs, only the 17 miRNA-based expression clustering was considered an independent prognostic factor for 5-year event-free survival (EFS) compared to other clinicopathological features. In conclusion, our study reports for the first time associations between miRNA profiles and childhood ACT prognosis, providing evidence that miRNAs could be useful biomarkers to discriminate patients with favorable and unfavorable clinical outcomes.
儿科肾上腺皮质肿瘤 (ACT) 是一种罕见的侵袭性肿瘤,具有异质性的预后。尽管进行了广泛的努力,但识别儿科 ACT 患者可靠的预后因素仍然是一个挑战。微小 RNA (miRNA) 特征与多种癌症的诊断、治疗反应和预后相关。然而,miRNA 在儿科 ACT 中的作用尚未得到充分探索。在这项研究中,我们对 37 例儿科 ACT 和 9 例非肿瘤性肾上腺 (NNA) 样本进行了 miRNA 微阵列分析,并使用 Kaplan-Meier 图、对数秩检验和 Cox 回归分析评估了异常表达 miRNA 的预后意义。我们总共鉴定出 98 个异常表达的 miRNA;它们的表达谱可区分 ACT 和 NNAs。在 98 个失调的 miRNA 中,有 17 个与患者的生存显著相关。此外,hsa-miR-630、-139-3p、-125a-3p、-574-5p、-596、-564、-1321 和 -423-5p 的高表达水平和 hsa-miR-377-3p、-126-3p、-410、-136-3p、-29b-3p、-29a-3p、-337-5p、-143-3p 和 -140-5p 的低表达水平与不良预后、肿瘤复发和/或死亡显著相关。重要的是,这些 17 个 miRNA 的表达谱将患者分为两组,具有不同的临床结局。尽管一些单独的 miRNA 在 ACT 中具有潜在的预后价值,但与其他临床病理特征相比,只有基于这 17 个 miRNA 的表达聚类被认为是 5 年无事件生存率 (EFS) 的独立预后因素。总之,我们的研究首次报道了 miRNA 谱与儿童 ACT 预后之间的关联,为 miRNA 可作为区分具有良好和不良临床结局的患者的有用生物标志物提供了证据。