| Literature DB >> 23821659 |
Alessandra Ferrajoli1, Tait D Shanafelt, Cristina Ivan, Masayoshi Shimizu, Kari G Rabe, Nazila Nouraee, Mariko Ikuo, Asish K Ghosh, Susan Lerner, Laura Z Rassenti, Lianchun Xiao, Jianhua Hu, James M Reuben, Steliana Calin, M James You, John T Manning, William G Wierda, Zeev Estrov, Susan O'Brien, Thomas J Kipps, Michael J Keating, Neil E Kay, George A Calin.
Abstract
Noncoding RNAs play a pivotal role in the pathogenesis of chronic lymphocytic leukemia (CLL). We hypothesized that microRNAs (miRs) are involved in the transition from monoclonal B-cell lymphocytosis (MBL) to CLL and tested miR-15a/16-1 cluster, miR-21, and miR-155 expression in purified B cells of normal individuals, individuals with MBL, and patients with CLL. When we analyzed 224 samples from 2 independent training and validation cohorts, we found that miR-155 was overexpressed in B cells from individuals with MBL, and even more so in B cells from patients with CLL, when compared with B cells from normal individuals. Furthermore, we were able to identify miR-155 in circulating microvesicles from both individuals with MBL and patients with CLL. Next, to examine the prognostic role of miR-155, we measured its expression level in plasma samples collected before treatment initiation in 228 patients with CLL. We found significantly higher miR-155 expression levels in patients who failed to achieve a complete response compared with those who experienced complete response. Our findings support the use of cellular and plasma levels of miR-155 as biomarkers for the risk of progression in individuals with MBL, as well as to identify patients with CLL who may not respond well to therapy.Entities:
Mesh:
Substances:
Year: 2013 PMID: 23821659 PMCID: PMC3779381 DOI: 10.1182/blood-2013-01-478222
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113