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Title

MiRNA expression profile of chronic lymphocytic leukemia patients with 13q deletion

AuthorsHernández-Sánchez, María; Rodríguez-Vicente, Ana Eugenia; Hernández, José Ángel; Lumbreras, Eva ; Sarasquete, María Eugenia; Martín, Ana-África; Benito, Rocío; Vicente-Gutiérrez, Carlos; Robledo, Cristina; Heras, Natalia de las; Rodríguez, Juan-Nicolas; Alcoceba, Miguel; García de Coca, Alfonso; Aguilar, Carlos; González, Marcos ; Hernández, Jesús M.
KeywordsmiRNA
13q deletion
CLL
Array
Expression
Issue Date2016
PublisherElsevier
CitationLeukemia Research 46: 30-36 (2016)
AbstractDeletion 13q (13q-) is the most common cytogenetic aberration in chronic lymphocytic leukemia (CLL) and is associated with the most favorable prognosis as the sole cytogenetic abnormality. However, it is heterogeneous whereby CLL patients with higher percentages of 13q- cells (13q-H) have a more aggressive clinical course and a distinct gene expression profile. The microRNA (miRNA) expression profile of CLL gives additional biological and prognostic information, but its expression in 13q- CLL has not been examined in detail. The miRNA expression of clonal B cell lymphocytes (CD19+ cells) of 38 CLL patients and normal B cells of six healthy donors was analyzed. CLL patients with higher percentages of 13q- cells (≥80%) showed a different level of miRNA expression from patients with lower percentages (<80%). Interestingly, miR-143 was downregulated and miR-155 was overexpressed in 13q-H. This deregulation affected important validated target genes involved in apoptosis (BCL2, MDM2, TP53INP1) and proliferation (KRAS, PI3K-AKT signaling), that could lead to decreased apoptosis and increased proliferation in 13q-H patients. This study provides new evidence about the heterogeneity of the 13q deletion in CLL patients, showing that miRNA regulation could be involved in several significant pathways deregulated in CLL patients with a high number of losses in 13q.
URIhttp://hdl.handle.net/10261/168627
Identifiersdoi: 10.1016/j.leukres.2016.04.008
e-issn: 1873-5835
issn: 0145-2126
Appears in Collections:(IBMCC) Artículos
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