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NEAT1 Long Isoform Is Highly Expressed in Chronic Lymphocytic Leukemia Irrespectively of Cytogenetic Groups or Clinical Outcome.

Authors :
Ronchetti, Domenica
Favasuli, Vanessa
Monti, Paola
Cutrona, Giovanna
Fabris, Sonia
Silvestris, Ilaria
Agnelli, Luca
Colombo, Monica
Menichini, Paola
Matis, Serena
Gentile, Massimo
Nurtdinov, Ramil
Guigó, Roderic
Baldini, Luca
Fronza, Gilberto
Ferrarini, Manlio
Morabito, Fortunato
Neri, Antonino
Taiana, Elisa
Source :
Non-Coding RNA. Mar2020, Vol. 6 Issue 1, p1-9. 9p.
Publication Year :
2020

Abstract

The biological role and therapeutic potential of long non-coding RNAs (lncRNAs) in chronic lymphocytic leukemia (CLL) are still open questions. Herein, we investigated the significance of the lncRNA NEAT1 in CLL. We examined NEAT1 expression in 310 newly diagnosed Binet A patients, in normal CD19+ B-cells, and other types of B-cell malignancies. Although global NEAT1 expression level was not statistically different in CLL cells compared to normal B cells, the median ratio of NEAT1_2 long isoform and global NEAT1 expression in CLL samples was significantly higher than in other groups. NEAT1_2 was more expressed in patients carrying mutated IGHV genes. Concerning cytogenetic aberrations, NEAT1_2 expression in CLL with trisomy 12 was lower with respect to patients without alterations. Although global NEAT1 expression appeared not to be associated with clinical outcome, patients with the lowest NEAT1_2 expression displayed the shortest time to first treatment; however, a multivariate regression analysis showed that the NEAT1_2 risk model was not independent from other known prognostic factors, particularly the IGHV mutational status. Overall, our data prompt future studies to investigate whether the increased amount of the long NEAT1_2 isoform detected in CLL cells may have a specific role in the pathology of the disease. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
2311553X
Volume :
6
Issue :
1
Database :
Academic Search Index
Journal :
Non-Coding RNA
Publication Type :
Academic Journal
Accession number :
142731781
Full Text :
https://doi.org/10.3390/ncrna6010011