| Literature DB >> 18977326 |
Huating Wang1, Ramiro Garzon, Hao Sun, Katherine J Ladner, Ravi Singh, Jason Dahlman, Alfred Cheng, Brett M Hall, Stephen J Qualman, Dawn S Chandler, Carlo M Croce, Denis C Guttridge.
Abstract
Studies support the importance of microRNAs in physiological and pathological processes. Here we describe the regulation and function of miR-29 in myogenesis and rhabdomyosarcoma (RMS). Results demonstrate that in myoblasts, miR-29 is repressed by NF-kappaB acting through YY1 and the Polycomb group. During myogenesis, NF-kappaB and YY1 downregulation causes derepression of miR-29, which in turn accelerates differentiation by targeting its repressor YY1. However, in RMS cells and primary tumors that possess impaired differentiation, miR-29 is epigenetically silenced by an activated NF-kappaB-YY1 pathway. Reconstitution of miR-29 in RMS in mice inhibits tumor growth and stimulates differentiation, suggesting that miR-29 acts as a tumor suppressor through its promyogenic function. Together, these results identify a NF-kappaB-YY1-miR-29 regulatory circuit whose disruption may contribute to RMS.Entities:
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Year: 2008 PMID: 18977326 PMCID: PMC3829205 DOI: 10.1016/j.ccr.2008.10.006
Source DB: PubMed Journal: Cancer Cell ISSN: 1535-6108 Impact factor: 31.743