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

被引:91
作者
Tili, Esmerina [1 ,2 ]
Michaille, Jean-Jacques [1 ,2 ,3 ]
Luo, Zhenghua [1 ,2 ]
Volinia, Stefano [1 ,2 ]
Rassenti, Laura Z. [4 ]
Kipps, Thomas J. [4 ]
Croce, Carlo M. [1 ,2 ]
机构
[1] Ohio State Univ, Dept Mol Virol Immunol & Med Genet, Med Ctr, Columbus, OH 43210 USA
[2] Ohio State Univ, Ctr Comprehens Canc, Columbus, OH 43210 USA
[3] Univ Bourgogne, Fac Gabriel, Biol Peroxysome Inflammat & Metab Lipid Inserm U8, Dijon, France
[4] Univ Calif San Diego, Moores Canc Ctr, Chron Lymphocyt Leukemias Res Consortium, La Jolla, CA 92093 USA
关键词
TUMOR-SUPPRESSOR; BREAST-CANCER; PROLIFERATION; INFLAMMATION; MICRORNAS; EXPRESSION; SIGNATURES; PATHWAYS;
D O I
10.1182/blood-2012-03-415737
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
MiR-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. (Blood. 2012; 120(13):2631-2638)
引用
收藏
页码:2631 / 2638
页数:8
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