Keywords:
Histone-Lysine; genetics; metabolism; brain neoplasms; pathology; drug effects; glioblastoma; enzymology; cell survival; antineoplastic agents
Abstract:
Chemotherapy often kills a large fraction of cancer cells but leaves behind a small population of drug-tolerant persister cells. These persister cells survive drug treatments through reversible, non-genetic mechanisms and cause tumour recurrence upon cessation of therapy. Here, we report a drug tolerance mechanism regulated by the germ-cell-specific H3K4 methyltransferase PRDM9.