Virus-encoded microRNA contributes to the molecular profile of EBV-positive Burkitt lymphomas

Claudio Tripodo, Stefano Lazzi, Maria Raffaella Ambrosio, Maria Rosaria Sapienza, Emily A. Rogena, Jessica Consiglio, Maria Antonella Laginestra, Mohsen Navari, Stefano A. Pileri, Maryam Etebari, Fabio Fuligni, Maura Rossi, Claudio Tripodo, Giulia De Falco, Cristiana Bellan, Pier Paolo Piccaluga, Lorenzo Leoncini, Davide Gibellini, Carlo M. Croce, Lynnette Tumwine

Risultato della ricerca: Articlepeer review

22 Citazioni (Scopus)


Burkitt lymphoma (BL) is an aggressive neoplasm characterized by consistent morphology and phenotype, typical clinical behavior and distinctive molecular profile. The latter is mostly driven by the MYC over-expression associated with the characteristic translocation (8;14) (q24; q32) or with variant lesions. Additional genetic events can contribute to Burkitt Lymphoma pathobiology and retain clinical significance. A pathogenetic role for Epstein-Barr virus infection in Burkitt lymphomagenesis has been suggested; however, the exact function of the virus is largely unknown.In this study, we investigated the molecular profiles (genes and microRNAs) of Epstein-Barr virus-positive and -negative BL, to identify specific patterns relying on the differential expression and role of Epstein-Barr virus-encoded microRNAs.First, we found significant differences in the expression of viral microRNAs and in selected target genes. Among others, we identified LIN28B, CGNL1, GCET2, MRAS, PLCD4, SEL1L, SXX1, and the tyrosine kinases encoding STK10/STK33, all provided with potential pathogenetic significance. GCET2, also validated by immunohistochemistry, appeared to be a useful marker for distinguishing EBV-positive and EBV-negative cases. Further, we provided solid evidences that the EBV-encoded microRNAs (e.g. BART6) significantly mold the transcriptional landscape of Burkitt Lymphoma clones.In conclusion, our data indicated significant differences in the transcriptional profiles of EBV-positive and EBV-negative BL and highlight the role of virus encoded miRNA.
Lingua originaleEnglish
pagine (da-a)224-240
Numero di pagine17
Stato di pubblicazionePublished - 2016

All Science Journal Classification (ASJC) codes

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