| Literature DB >> 18327259 |
Changchun Xiao1, Lakshmi Srinivasan, Dinis Pedro Calado, Heide Christine Patterson, Baochun Zhang, Jing Wang, Joel M Henderson, Jeffrey L Kutok, Klaus Rajewsky.
Abstract
The genomic region encoding the miR-17-92 microRNA (miRNA) cluster is often amplified in lymphoma and other cancers, and cancer cells carrying this amplification have higher expression of miRNA in this cluster. Retroviral expression of miR-17-92 accelerates c-Myc-induced lymphoma development, but precisely how higher expression of miR-17-92 promotes lymphomagenesis remains unclear. Here we generated mice with higher expression of miR-17-92 in lymphocytes. These mice developed lymphoproliferative disease and autoimmunity and died prematurely. Lymphocytes from these mice showed more proliferation and less activation-induced cell death. The miR-17-92 miRNA suppressed expression of the tumor suppressor PTEN and the proapoptotic protein Bim. This mechanism probably contributed to the lymphoproliferative disease and autoimmunity of miR-17-92-transgenic mice and contributes to lymphoma development in patients with amplifications of the miR-17-92 coding region.Entities:
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Year: 2008 PMID: 18327259 PMCID: PMC2533767 DOI: 10.1038/ni1575
Source DB: PubMed Journal: Nat Immunol ISSN: 1529-2908 Impact factor: 25.606