Homologous recombination repair deficiency in histone H3 lysine 27-to-methionine diffuse midline glioma (H3K27M DMG) can be therapeutically leveraged with PARP inhibitors to radiosensitize and induce an NK cell-mediated antitumor immune response selectively in H3K27M DMG, supporting the clinical investigation of PARP1 inhibitors with radiotherapy in DMG patients.
[Neuro-Oncology]

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