Barretos Children's Cancer Hospital from Hospital de Amor, Brazil.
Brazilian Childhood Germ Cell Tumor Study Group, The Brazilian Pediatric Oncology Society (SOBOPE), São Paulo, Brazil.
Mol Oncol. 2024 Jun;18(6):1593-1607. doi: 10.1002/1878-0261.13617. Epub 2024 May 9.
microRNAs (miRNAs) are small endogenous noncoding RNAs, and alterations in their expression may contribute to oncogenesis. Discovering a unique miRNA pattern holds the potential for early detection and novel treatment possibilities in cancer. This study aimed to evaluate miRNA expression in pediatric patients with gonadal germ cell tumors (GCTs), focusing on characterizing the miRNA profiles of each histological subtype and identifying a distinct histological miRNA signature for a total of 42 samples of pediatric gonadal GCTs. The analysis revealed distinct miRNA expression profiles for all histological types, regardless of the primary site. We identified specific miRNA expression signatures for each histological type, including 34 miRNAs for dysgerminomas, 13 for embryonal carcinomas, 25 for yolk sac tumors, and one for immature teratoma, compared to healthy controls. Furthermore, we identified 26 miRNAs that were commonly expressed in malignant tumors, with six miRNAs (miR-302a-3p, miR-302b-3p, miR-371a-5p, miR-372-3p, miR-373-3p, and miR-367-3p) showing significant overexpression. Notably, miR-302b-3p exhibited a significant association with all the evaluated clinical features. Our findings suggest that miRNAs have the potential to aid in the diagnosis, prognosis, and management of patients with malignant GCTs.
微小 RNA(miRNA)是小型内源性非编码 RNA,其表达的改变可能有助于肿瘤的发生。发现独特的 miRNA 模式有可能实现癌症的早期检测和新的治疗可能性。本研究旨在评估儿童性腺生殖细胞肿瘤(GCT)患者的 miRNA 表达,重点是描述每种组织学亚型的 miRNA 图谱,并确定总共 42 个儿童性腺 GCT 样本的独特组织学 miRNA 特征。分析显示,所有组织学类型都存在不同的 miRNA 表达谱,无论原发部位如何。我们确定了每种组织学类型的特定 miRNA 表达特征,包括 34 个用于无性细胞瘤,13 个用于胚胎癌,25 个用于卵黄囊瘤,1 个用于未成熟畸胎瘤,与健康对照组相比。此外,我们确定了 26 个在恶性肿瘤中共同表达的 miRNA,其中 6 个 miRNA(miR-302a-3p、miR-302b-3p、miR-371a-5p、miR-372-3p、miR-373-3p 和 miR-367-3p)表现出显著过表达。值得注意的是,miR-302b-3p 与所有评估的临床特征均显著相关。我们的研究结果表明,miRNA 有可能有助于恶性 GCT 患者的诊断、预后和管理。