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Potential diagnostic and prognostic biomarkers of pediatric Burkitt lymphoma identified through miRNA expression profiling.
Küçük, Can; Esmeray Sönmez, Esra; Hatipoglu, Tevfik; Yuan, Hongling; Hu, Xiaozhou; Ceylan, Arda; Sivis, Zuhal Önder; Demirag, Bengü; Ataseven, Eda; Ince, Dilek; Altun, Zekiye; Aktas, Safiye; Özsan, Nazan; Erdag, Taner Kemal; Ayhan, Yavuz Selim; Demir Gündogan, Begümhan; Çetingül, Nazan; Özer, Erdener; Kutluk, Tezer; Olgun, Nur.
Afiliação
  • Küçük C; Department of Medical Biology, Faculty of Medicine, Dokuz Eylül University, Izmir, Türkiye. can.kucuk@deu.edu.tr.
  • Esmeray Sönmez E; Izmir Biomedicine and Genome Center, Izmir, Türkiye. can.kucuk@deu.edu.tr.
  • Hatipoglu T; Izmir Biomedicine and Genome Center, Izmir, Türkiye.
  • Yuan H; Izmir International Biomedicine and Genome Institute, Dokuz Eylül University, Izmir, Türkiye.
  • Hu X; Izmir Biomedicine and Genome Center, Izmir, Türkiye.
  • Ceylan A; Izmir International Biomedicine and Genome Institute, Dokuz Eylül University, Izmir, Türkiye.
  • Sivis ZÖ; Department of Basic Oncology, Oncology Institute, Dokuz Eylül University, Izmir, Türkiye.
  • Demirag B; Department of Medical Biochemistry, Faculty of Medicine, Dokuz Eylül University, Izmir, Türkiye.
  • Ataseven E; Izmir Biomedicine and Genome Center, Izmir, Türkiye.
  • Ince D; Izmir International Biomedicine and Genome Institute, Dokuz Eylül University, Izmir, Türkiye.
  • Altun Z; Izmir Tepecik Education and Research Hospital, Health Sciences University, Izmir, Türkiye.
  • Aktas S; Dr. Behçet Uz Pediatric Diseases and Surgery Training and Research Hospital, Health Sciences University, Izmir, Türkiye.
  • Özsan N; Department of Child Health and Diseases, Faculty of Medicine, Ege University, Izmir, Türkiye.
  • Erdag TK; Department of Clinical Oncology, Oncology Institute, Dokuz Eylül University, Izmir, Türkiye.
  • Ayhan YS; Department of Basic Oncology, Oncology Institute, Dokuz Eylül University, Izmir, Türkiye.
  • Demir Gündogan B; Department of Basic Oncology, Oncology Institute, Dokuz Eylül University, Izmir, Türkiye.
  • Çetingül N; Department of Medical Pathology, Ege University, Izmir, Türkiye.
  • Özer E; Department of Otorhinolaryngology, Dokuz Eylül University School of Medicine, Izmir, Türkiye.
  • Kutluk T; Department of Child Health and Diseases, Faculty of Medicine, Mersin University, Mersin, Türkiye.
  • Olgun N; Department of Child Hematology and Oncology, Faculty of Medicine, Mersin University, Mersin, Türkiye.
Pediatr Res ; 2024 Sep 11.
Article em En | MEDLINE | ID: mdl-39261659
ABSTRACT

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.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article