RB loss sensitizes cells to replication-associated DNA damage after PARP inhibition by trapping.

ABSTRACT: The retinoblastoma tumor suppressor protein (RB) interacts physically and functionally with a number of epigenetic modifying enzymes to control transcriptional regulation, respond to replication stress, promote DNA damage response and repair, and regulate genome stability. To better understand how disruption of RB function impacts epigenetic regulation of genome stability and determine whether such changes represent exploitable weaknesses of RB-deficient cancer cells, we performed an imaging-based screen to identify epigenetic inhibitors that promote DNA damage and compromise the viability of RB-deficient cells. We found that loss of RB alone leads to high levels of replication-dependent poly-ADP ribosylation (PARylation) and that preventing PARylation by trapping PARP enzymes on chromatin

SUBMITTER: Zamalloa LG 

PROVIDER: S-EPMC10500056 | biostudies-literature | 2023 Dec

REPOSITORIES: biostudies-literature