| Literature DB >> 11896599 |
Pedro Antonio Pérez-Mancera1, Jesus Pérez-Losada, Manuel Sánchez-Martín, Maria Aranzazu Rodríguez-García, Teresa Flores, Enrique Battaner, Alfonso Gutiérrez-Adán, Belen Pintado, Isidro Sánchez-García.
Abstract
Fusion proteins created by chromosomal abnormalities are key components of mesenchymal cancer development. The most common chromosomal translocation in liposarcomas, t(12;16)(q13;p11), creates the FUS-CHOP fusion gene. In the past, we generated FUS-CHOP and CHOP transgenic mice and have shown that while FUS-CHOP transgenic develop liposarcomas, mice expressing CHOP, which lacks the FUS domain, display essentially normal white adipose tissue (WAT) development, suggesting that the FUS domain of FUS-CHOP plays a specific and critical role in the pathogenesis of liposarcoma. To test the significance of FUS and CHOP domain interactions within a living mouse, we generated mice expressing the FUS domain and crossed them with CHOP-transgenic mice to generate double-transgenic FUSxCHOP animals. Here we report that expression of the FUS domain restores liposarcoma development in CHOP-transgenic mice. Our results provide genetic evidence that FUS and CHOP domains function in trans for the mutual restoration of liposarcoma. These results identify a new mechanism of tumor-associated fusion genes and might have impact beyond myxoid liposarcoma.Entities:
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Year: 2002 PMID: 11896599 DOI: 10.1038/sj.onc.1205220
Source DB: PubMed Journal: Oncogene ISSN: 0950-9232 Impact factor: 9.867