Literature DB >> 17178851

Tcl1 expression in chronic lymphocytic leukemia is regulated by miR-29 and miR-181.

Yuri Pekarsky1, Urmila Santanam, Amelia Cimmino, Alexey Palamarchuk, Alexey Efanov, Vadim Maximov, Stefano Volinia, Hansjuerg Alder, Chang-Gong Liu, Laura Rassenti, George A Calin, John P Hagan, Thomas Kipps, Carlo M Croce.   

Abstract

B-cell chronic lymphocytic leukemia (B-CLL) is the most common human leukemia in the world. Deregulation of the TCL1 oncogene is a causal event in the pathogenesis of the aggressive form of this disease as was verified by using animal models. To study the mechanism of Tcl1 regulation in CLL, we carried out microRNA expression profiling of three types of CLL: indolent CLL, aggressive CLL, and aggressive CLL showing 11q deletion. We identified distinct microRNA signatures corresponding to each group of CLL. We further determined that Tcl1 expression is regulated by miR-29 and miR-181, two microRNAs differentially expressed in CLL. Expression levels of miR-29 and miR-181 generally inversely correlated with Tcl1 expression in the CLL samples we examined. Our results suggest that Tcl1 expression in CLL is, at least in part, regulated by miR-29 and miR-181 and that these microRNAs may be candidates for therapeutic agents in CLLs overexpressing Tcl1.

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Year:  2006        PMID: 17178851     DOI: 10.1158/0008-5472.CAN-06-3613

Source DB:  PubMed          Journal:  Cancer Res        ISSN: 0008-5472            Impact factor:   12.701


  250 in total

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9.  MiR-181 mediates cell differentiation by interrupting the Lin28 and let-7 feedback circuit.

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10.  MicroRNAs as new players in the genomic galaxy and disease puzzles.

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