The down-regulation of miR-125b in chronic lymphocytic leukemias leads to metabolic adaptation of cells to a transformed state

Author:

Tili Esmerina1,Michaille Jean-Jacques12,Luo Zhenghua1,Volinia Stefano1,Rassenti Laura Z.3,Kipps Thomas J.3,Croce Carlo M.1

Affiliation:

1. Department of Molecular Virology, Immunology and Medical Genetics, The Ohio State University Medical Center and Comprehensive Cancer Center, Columbus, OH;

2. Biologie du Peroxysome, de l'Inflammation et du Métabolisme Lipidique Inserm U866, Université de Bourgogne, Faculté Gabriel, Dijon, France; and

3. Chronic Lymphocytic Leukemias Research Consortium, University of California, San Diego, Moores Cancer Center, La Jolla, CA

Abstract

AbstractMiR-125b-1 maps at 11q24, a chromosomal region close to the epicenter of 11q23 deletions in chronic lymphocytic leukemias (CLLs). Our results establish that both aggressive and indolent CLL patients show reduced expression of miR-125b. Overexpression of miR-125b in CLL-derived cell lines resulted in the repression of many transcripts encoding enzymes implicated in cell metabolism. Metabolomics analyses showed that miR-125b overexpression modulated glucose, glutathione, lipid, and glycerolipid metabolism. Changes on the same metabolic pathways also were observed in CLLs. We furthermore analyzed the expression of some of miR-125b–target transcripts that are potentially involved in the aforementioned metabolic pathways and defined a miR-125b–dependent CLL metabolism-related transcript signature. Thus, miR-125b acts as a master regulator for the adaptation of cell metabolism to a transformed state. MiR-125b and miR-125b–dependent metabolites therefore warrant further investigation as possible novel therapeutic approaches for patients with CLL.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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