Nature Communications (Dec 2021)
Therapeutic vulnerability to PARP1,2 inhibition in RB1-mutant osteosarcoma
Abstract
RB1 mutations are seen in 40-60% of sporadic osteosarcoma. Here, the authors demonstrate a selective sensitivity to PARP inhibitors in RB1-mutated osteosarcoma-derived cell lines that is not associated with canonical signatures indicative of a homologous recombination defect.