| Literature DB >> 21685371 |
Sabine Teichler1, Thomas Illmer, Josephine Roemhild, Dmitriy Ovcharenko, Thorsten Stiewe, Andreas Neubauer.
Abstract
MicroRNAs (miRNAs) are small, noncoding RNA molecules that regulate growth and differentiation. miRNAs are frequently located at cancer-specific fragile sites in the human genome, such as chromosome 7q. The nuclear oncogene SKI is up-regulated in acute myeloid leukemia (AML) with -7/del7q. Here we asked whether loss of miRNAs on chromosome 7q may explain this up-regulation. miR-29a expression was found to be down-regulated in AML with -7/del7q. Forced expression of miR-29a down-regulated Ski and its target gene, Nr-CAM, whereas miR-29a inhibition induced Ski expression. Luciferase assays validated a functional binding site for miR-29a in the 3' untranslated region of SKI. Finally, in samples of AML patients, we observed an inverse correlation of Ski and miR-29a expression, respectively. In conclusion, up-regulation of Ski in AML with -7/del7q is caused by loss of miR-29a. miR-29a may therefore function as an important tumor suppressor in AML by restraining expression of the SKI oncogene.Entities:
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Year: 2011 PMID: 21685371 DOI: 10.1182/blood-2010-09-306258
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113