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Our study, Targeting TRIP13 in favorable histology Wilms tumor with nuclear export inhibitors synergizes with doxorubicin, is published in Communications Biology.

The work establishes patient-derived Wilms tumor cell lines as faithful preclinical models, identifies XPO1 as a therapeutic vulnerability through loss-of-function screening, and demonstrates that combining the FDA-approved XPO1 inhibitor KPT-330 with doxorubicin produces durable remissions in vivo — findings that have contributed to an active Phase II clinical trial NCT05985161.

The manuscript can be found online.

Conference photo