NF-κB-YY1-miR-29 Regulatory Circuitry in Skeletal Myogenesis and Rhabdomyosarcoma

被引:487
作者
Wang, Huating [1 ]
Garzon, Ramiro [1 ]
Sun, Hao [1 ]
Ladner, Katherine J. [1 ]
Singh, Ravi [2 ]
Dahlman, Jason [1 ]
Cheng, Alfred [1 ]
Hall, Brett M. [2 ]
Qualman, Stephen J. [2 ]
Chandler, Dawn S. [2 ]
Croce, Carlo M. [1 ,3 ]
Guttridge, Denis C. [1 ,3 ]
机构
[1] Ohio State Univ, Dept Mol Virol Immunol & Med Genet, Human Canc Genet Program, Columbus, OH 43210 USA
[2] Ohio State Univ, Nationwide Childrens Hosp, Dept Pediat, Columbus, OH 43210 USA
[3] Ohio State Univ, Arthur G James Comprehens Canc Ctr, Columbus, OH 43210 USA
关键词
D O I
10.1016/j.ccr.2008.10.006
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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-kappa B acting through YY1 and the Polycomb group. During myogenesis, NF-kappa B 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-kappa B-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-kappa B-YY1-miR-29 regulatory circuit whose disruption may contribute to RMS.
引用
收藏
页码:369 / 381
页数:13
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