Abstract
SIGNIFICANCE
Targeting TDP2 or DNA-PKcs synergizes with low-dose doxorubicin to induce p53-mediated senescence and sensitivity to senolytics in MDM2-amplified liposarcoma, meriting therapeutic exploration.
UNLABELLED
Dedifferentiated liposarcoma (DDLPS) is a rare cancer defined by amplification of mouse double minute 2 (MDM2) and cyclin-dependent kinase (CDK) 4. Conventional chemotherapy (doxorubicin) and targeted inhibition of MDM2 and CDK4 show sporadic responses, but most tumors display primary resistance. In this study, we used an unbiased approach to identify therapeutic strategies sensitizing to these DDLPS therapies. Three parallel genome-wide CRISPR-Cas9 knockout screens were conducted in DDLPS cells to sensitize to palbociclib (CDK4 inhibitor), nutlin-3a (MDM2 inhibitor), or doxorubicin. Top screen hits were validated and characterized in both in vitro and in vivo models, whereas clinical data were used to corroborate molecular findings. Inactivation of genes related to G1-S transition (CDK2, CKS1B, E2F3, and CCNE1) and non-homologous end joining (NHEJ; TDP2, PRKDC, and XRCC4) enhanced sensitivity to palbociclib and doxorubicin, respectively. Genetic perturbation of TDP2 or pharmacologic inhibition of DNA-dependent kinase catalytic subunit (DNA-PKcs) using peposertib synergized with prolonged administration of low-dose doxorubicin to induce cell-cycle arrest and senescence, and subsequent senolytic treatment with Bcl-2 inhibitor navitoclax triggered senescent cells to undergo apoptosis. Despite the amplification of MDM2, senescence was mediated by p53. Consistently, The Cancer Genome Atlas (TCGA) and DepMap data suggested p53 activity in DDLPS. These findings provide a rationale for targeting the NHEJ pathway to enhance the efficacy of low-dose doxorubicin in DDLPS, highlighting a potential therapeutic strategy exploiting p53-mediated cell-cycle arrest and senescence. Furthermore, this study provides evidence that baseline p53 activity is preserved in DDLPS despite MDM2 amplification.