微小RNA在儿童生殖细胞肿瘤诊断和监测中的应用:哈萨克斯坦经验。

IF 1.2 4区 医学 Q4 HEMATOLOGY Pediatric Hematology and Oncology Pub Date : 2024-01-01 Epub Date: 2024-02-10 DOI:10.1080/08880018.2023.2267607
Symbat Saliyeva, Riza Boranbayeva, Minira Bulegenova, Vyacheslav Beloussov
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引用次数: 0

摘要

GCT的特征是特异性生物化学标志物的表达,如人绒毛膜促性腺激素(hCG)和甲胎蛋白(AFP),这是诊断和监测GCT治疗的主要工具。它们在15-20%的精原细胞瘤病例和60-80%的非精原细胞癌病例中表达。MicroRNA图谱可以识别出许多在原发性肿瘤诊断以及随后的复发监测和预测中优于经典血清肿瘤标志物的微小RNA。我们分析了20名患有颅外GCT的儿童在不同治疗阶段血清中9种微小RNA(微小RNA簇302/367和371-373,微小RNA375)的表达,并显示了它们在早期检测事件中的有用性和信息性。考虑到其高灵敏度和特异性,血清微小RNA 367371372373302d在恶性GCT的临床应用具有重要意义。在恶性GCT或畸胎瘤中均未检测到miR 375-3p的显著表达。
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Application of microRNAs in the diagnosis and monitoring of pediatric germ cell tumors: Kazakh experience.

GCT is characterized by specific biochemical markers expression, such as human chorionic gonadotropin (hCG) and alpha-fetoprotein (AFP), which are the main tools in the diagnosis and monitoring of GCT treatment. They are expressed in 15-20% of cases of seminoma and in 60-80% of cases of non-seminoma. MicroRNA profiling allows to identify a number of microRNAs that are superior to classical serum tumor markers in the diagnosis of primary tumors, as well as in subsequent monitoring and prediction of recurrence. We analyzed the expression of 9 microRNAs (microRNA clusters 302/367 and 371-373, microRNA375) in the blood serum of 20 children with extracranial GCT at different stages of therapy and showed their usefulness and informativeness in early detection of events. Taking into consideration the high sensitivity and specificity, serum microRNAs 367,371,372,373,302d are of great interest for clinical use in malignant GCT. Significant expression of miR 375-3p was not detected either in malignant GCT or in teratomas.

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来源期刊
CiteScore
2.60
自引率
5.90%
发文量
71
审稿时长
6-12 weeks
期刊介绍: PHO: Pediatric Hematology and Oncology covers all aspects of research and patient management within the area of blood disorders and malignant diseases of childhood. Our goal is to make PHO: Pediatric Hematology and Oncology the premier journal for the international community of clinicians and scientists who together aim to define optimal therapeutic strategies for children and young adults with cancer and blood disorders. The journal supports articles that address research in diverse clinical settings, exceptional case studies/series that add novel insights into pathogenesis and/or clinical care, and reviews highlighting discoveries and challenges emerging from consortia and conferences. Clinical studies as well as basic and translational research reports regarding cancer pathogenesis, genetics, molecular diagnostics, pharmacology, stem cells, molecular targeting, cellular and immune therapies and transplantation are of interest. Papers with a focus on supportive care, late effects and on related ethical, legal, psychological, social, cultural, or historical aspects of these fields are also appreciated. Reviews on important developments in the field are welcome. Articles from scientists and clinicians across the international community of Pediatric Hematology and Oncology are considered for publication. The journal is not dependent on or connected with any organization or society. All submissions undergo rigorous peer review prior to publication. Our Editorial Board includes experts in Pediatric Hematology and Oncology representing a wide range of academic and geographic diversity.
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