Salzmann Rebekka J S, Garbin Anna, Gaffo Enrico, Elia Caterina, Martire Gaia, Bortoluzzi Stefania, Tondo Annalisa, Muggeo Paola, Sala Alessandra, Pizzi Marco, Pillon Marta, Carraro Elisa, Lopci Egesta, de Re Valli, Mascarin Maurizio, Mussolin Lara
Istituto di Ricerca Pediatrica "Città della Speranza", 35128 Padua, Italy.
Maternal and Child Health Department Pediatric Hematology, Oncology and Stem Cell Transplant Center, University of Padua, 35128 Padua, Italy.
Int J Mol Sci. 2024 Dec 10;25(24):13243. doi: 10.3390/ijms252413243.
Currently, risk stratification for pediatric Hodgkin lymphoma is based on clinical factors such as stage, bulk, and systemic symptoms. Novel minimally invasive biomarkers could enhance both prognosis and treatment strategies. Therefore, the plasma extracellular vesicles' microRNA profile was characterized by small RNA sequencing in 36 classical Hodgkin lymphoma cases and these findings were confirmed in an extended cohort of 86 patients by RT-qPCR. It was found that the levels of miR-122-5p at diagnosis were significantly higher -value: 0.0002) in patients who relapsed compared to patients in remission. The 5-year event-free survival of cases with high and low levels of miR-122-5p was 65 ± 7% and 93 ± 4%, respectively. MiR-122-5p levels were significantly associated with clinical events in both univariate -value: 0.0009) and multivariate -value: 0.0037) analysis (hazard ratio 5.8). Target prediction analysis suggests an involvement in the polarization of immune cells. The phenotypic characterization of peripheral blood mononuclear cells in 12 patients showed significantly increased levels of CD4+ T-cells in cases with high miR-122-5p levels as compared to low levels -value: 0.048). Moreover, CCL17 (TARC) and IL-6 plasma levels at diagnosis were significantly higher as compared to healthy donors -value: ≤0.0001). MiR-122-5p could complement current prognostic assays to identify patients at high risk of relapse.
目前,儿童霍奇金淋巴瘤的风险分层基于临床因素,如分期、肿块大小和全身症状。新型微创生物标志物可改善预后并优化治疗策略。因此,通过小RNA测序对36例经典型霍奇金淋巴瘤病例的血浆细胞外囊泡微小RNA谱进行了表征,并通过RT-qPCR在86例患者的扩展队列中证实了这些发现。结果发现,复发患者诊断时的miR-122-5p水平显著高于缓解患者(P值:0.0002)。miR-122-5p水平高低的病例5年无事件生存率分别为65±7%和93±4%。在单因素分析(P值:0.0009)和多因素分析(P值:0.0037)中,miR-122-5p水平均与临床事件显著相关(风险比5.8)。靶标预测分析表明其参与免疫细胞极化。对12例患者外周血单个核细胞的表型特征分析显示,miR-122-5p水平高的病例中CD4+T细胞水平显著高于低水平病例(P值:0.048)。此外,诊断时CCL17(TARC)和IL-6血浆水平显著高于健康供者(P值:≤0.0001)。miR-122-5p可补充当前的预后检测方法,以识别复发高风险患者。