通过 miRNA 表达谱分析确定小儿伯基特淋巴瘤的潜在诊断和预后生物标志物

IF 3.1 3区 医学 Q1 PEDIATRICS Pediatric Research Pub Date : 2024-09-11 DOI:10.1038/s41390-024-03478-9
Can Küçük, Esra Esmeray Sönmez, Tevfik Hatipoğlu, Hongling Yuan, Xiaozhou Hu, Arda Ceylan, Zuhal Önder Siviş, Bengü Demirağ, Eda Ataseven, Dilek İnce, Zekiye Altun, Safiye Aktaş, Nazan Özsan, Taner Kemal Erdağ, Yavuz Selim Ayhan, Begümhan Demir Gündoğan, Nazan Çetingül, Erdener Özer, Tezer Kutluk, Nur Olgun
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引用次数: 0

摘要

背景小儿伯基特淋巴瘤(pBL)是儿童中最常见的非霍奇金淋巴瘤。由于肿瘤生长迅速,这些患者需要及时诊断和开始治疗。方法通过微RNA测序(miRNA-Seq)鉴定了诊断为pBL的肿瘤组织和血浆中差异表达(DE)的miRNA。通过接受者操作特征(ROC)分析评估了总miRNA浓度和过表达miRNA的诊断潜力。采用对数秩检验评估与DE miRNA相关的生存率差异。结果与对照组相比,pBL病例的循环细胞游离miRNA总数更高。在 pBL 肿瘤组织中差异表达的 miRNA 中,与癌症相关的通路较多。pBL 肿瘤中一些上调的 miRNA 具有很高的诊断潜力。同样,过表达血浆 miRNA 的 ROC 分析显示,循环中的无细胞或外泌体 miRNA 可将 pBL 与对照病例区分开来。事实上,对过表达循环外泌体 miRNA 的综合分析表明,某些三重组合的诊断潜力有所提高。结论 pBL 肿瘤组织和血浆中不同表达的 miRNAs 有可能改善诊断和预后。该研究首次应用miRNA-Seq技术对未经治疗的小儿伯基特淋巴瘤病例进行研究,以鉴定肿瘤组织和血浆样本中具有诊断潜力的差异表达miRNA。在小儿伯基特淋巴瘤病例中发现的具有临床意义的、差异表达的 miRNAs 有可能在诊断或预后方面改善目前基于组织或非侵入性的临床实践。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Potential diagnostic and prognostic biomarkers of pediatric Burkitt lymphoma identified through miRNA expression profiling

Background

Pediatric Burkitt lymphoma (pBL) is the most common non-Hodgkin lymphoma in children. These patients require prompt diagnosis and initiation of therapy due to rapid tumor growth. The roles of tumor tissue and circulating microRNAs (miRNAs) in the diagnosis or prognostication have not been fully elucidated in pBLs.

Methods

Differentially expressed (DE) miRNAs were identified with microRNA sequencing (miRNA-Seq) in tumor tissues and plasma of diagnostic pBLs. The diagnostic potential of total miRNA concentrations and overexpressed miRNAs were evaluated through receiver operating characteristic (ROC) analyses. Log-rank test was employed to evaluate survival differences associated with DE miRNAs. Selected miRNA expressions were cross-validated with quantitative reverse transcription PCR (qRT-PCR).

Results

Total circulating cell-free miRNAs were higher in pBL cases compared to controls. Cancer-associated pathways were enriched among miRNAs differentially expressed in pBL tumor tissues. Several upregulated miRNAs in pBL tumors demonstrated high diagnostic potential. Similarly, ROC analysis of overexpressed plasma miRNAs revealed circulating cell-free or exosomal miRNAs that can distinguish pBLs from control cases. Indeed, integrative analysis of overexpressed circulating exosomal miRNAs showed an enhanced diagnostic potential for certain triple combinations. Kaplan–Meier analyses of DE miRNAs in tumor tissues identified miRNAs predicting overall survival.

Conclusions

Differentially expressed miRNAs in tumor tissue and plasma of pBL have the potential to improve diagnosis and prognosis.

Impact

  • Differentially expressed miRNAs in treatment-naive pediatric Burkitt lymphoma cases have diagnostic or prognostic biomarker potential.

  • This is the first study that applied miRNA-Seq on treatment-naive pediatric Burkitt lymphoma cases for identification of differentially expressed miRNAs both in tumor tissue and plasma samples with diagnostic potential.

  • Through systematic analysis of differentially expressed miRNAs, tumor tissue miRNAs associated with the overall survival of pBLs have been discovered.

  • The clinically significant, differentially expressed miRNAs identified in pediatric Burkitt lymphoma cases can potentially improve the current tissue-based or non-invasive clinical practice in terms of diagnosis or prognostication.

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来源期刊
Pediatric Research
Pediatric Research 医学-小儿科
CiteScore
6.80
自引率
5.60%
发文量
473
审稿时长
3-8 weeks
期刊介绍: Pediatric Research publishes original papers, invited reviews, and commentaries on the etiologies of children''s diseases and disorders of development, extending from molecular biology to epidemiology. Use of model organisms and in vitro techniques relevant to developmental biology and medicine are acceptable, as are translational human studies
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