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<dc:creator>Amaral, Ana Teresa</dc:creator>
<dc:creator>Garofalo, Cecilia</dc:creator>
<dc:creator>Frapolli, Roberta</dc:creator>
<dc:creator>Manara, María Cristina</dc:creator>
<dc:creator>Mancarella, Caterina</dc:creator>
<dc:creator>Uboldi, Sarah</dc:creator>
<dc:creator>Giandomenico, Silvana Di</dc:creator>
<dc:creator>Ordóñez García, José Luis</dc:creator>
<dc:creator>Sevillano, María Victoria</dc:creator>
<dc:creator>Malaguarnera, Roberta</dc:creator>
<dc:creator>Picci, Piero</dc:creator>
<dc:creator>Hassan, A. Bass</dc:creator>
<dc:creator>de Álava Casado, Enrique</dc:creator>
<dc:creator>D'Incalci, Maurizio</dc:creator>
<dc:creator>Scotlandi, Katia</dc:creator>
<dc:date>2015</dc:date>
<dc:description>[EN]Purpose: Goal of this study was to identify mechanisms that limit efficacy of trabectedin (ET-743, Yondelis) in Ewing sarcoma (EWS), so as to develop a clinical applicable combination therapy. Experimental Design: By chromatin immunoprecipitation, we analyzed EWS-FLI1 binding to the promoters of several target genes, such as TGFβR2, CD99, insulin-like growth factor receptor 1 (IGF1R), and IGF1, both in vitro and in xenografts treated with trabectedin or doxorubicin. Combined therapy with trabectedin and anti-IGF1R agents (AVE1642 HAb; OSI-906) was tested in vitro and in xenografts. Results: We confirm that both trabectedin and doxorubicin were able to strongly reduce EWS-FLI1 (both type I and type II) binding to two representative target genes ( TGFβR2 and CD99), both in vitro and in xenografts. However, trabectedin, but not doxorubicin, was also able to increase the occupancy of EWS-FLI1 to IGF1R promoters, leading to IGF1R upregulation. Inhibition of IGF1R either by the specific AVE1642 human antibody or by the dual IGF1R/insulin receptor inhibitor OSI-906 (Linsitinib) greatly potentiate the efficacy of trabectedin in the 13 EWS cell lines here considered as well as in TC-71 and 6647 xenografts. Combined therapy induced synergistic cytotoxic effects. Trabectedin and OSI-906 deliver complementary messages that likely converge on DNA-damage response and repair pathways. Conclusions: Weshowed that trabectedin may not only inhibit but also enhance the binding of EWS-FLI1 to certain target genes, leading to upregulation of IGF1R. We here provide the rationale for combining trabectedin to anti-IGF1R inhibitors.</dc:description>
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<dc:language>eng</dc:language>
<dc:publisher>American Association for Cancer Research</dc:publisher>
<dc:title>Trabectedin efficacy in Ewing sarcoma Is greatly increased by combination with anti-IGF signaling agents</dc:title>
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