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Intrinsic PARG inhibitor sensitivity is mimicked by TIMELESS haploinsufficiency and rescued by nucleoside supplementation

Title: Intrinsic PARG inhibitor sensitivity is mimicked by TIMELESS haploinsufficiency and rescued by nucleoside supplementation
Authors: Coulson-Gilmer, Camilla; Littler, Samantha; Barnes, Bethany M; Brady, Rosie M; Anagho, Holda A; Pillay, Nisha; Dey, Malini; Macmorland, William; Bronder, Daniel; Nelson, Louisa; Tighe, Anthony; Lin, Wei-Hsiang; Morgan, Robert D; Unwin, Richard D; Nielsen, Michael L; McGrail, Joanne C; Taylor, Stephen S
Contributors: Cancer Research UK Programme; Medical Research Council; NIHR Manchester Biomedical Research Centre; Cancer Research UK Manchester Centre; Department of Health and Social Care; Wellcome Trust; Novo Nordisk Foundation; Danish Council of Independent Research; Danish Cancer Institute; NNF Copenhagen Bioscience
Source: NAR Cancer ; volume 6, issue 3 ; ISSN 2632-8674
Publisher Information: Oxford University Press (OUP)
Publication Year: 2024
Description: A subset of cancer cells are intrinsically sensitive to inhibitors targeting PARG, the poly(ADP-ribose) glycohydrolase that degrades PAR chains. Sensitivity is accompanied by persistent DNA replication stress, and can be induced by inhibition of TIMELESS, a replisome accelerator. However, the nature of the vulnerability responsible for intrinsic sensitivity remains undetermined. To understand PARG activity dependency, we analysed Timeless model systems and intrinsically sensitive ovarian cancer cells. We show that nucleoside supplementation rescues all phenotypes associated with PARG inhibitor sensitivity, including replisome speed and fork stalling, S-phase completion and mitotic entry, proliferation dynamics and clonogenic potential. Importantly nucleoside supplementation restores PARG inhibitor resistance despite the continued presence of PAR chains, indicating that sensitivity does not correlate with PAR levels. In addition, we show that inhibition of thymidylate synthase, an enzyme required for dNTP homeostasis, induces PARG-dependency. Together, these observations suggest that PARG inhibitor sensitivity reflects an inability to control replisome speed and/or maintain helicase-polymerase coupling in response to nucleotide imbalances.
Document Type: article in journal/newspaper
Language: English
DOI: 10.1093/narcan/zcae030
Availability: https://doi.org/10.1093/narcan/zcae030; https://academic.oup.com/narcancer/article-pdf/6/3/zcae030/59042984/zcae030.pdf
Rights: https://creativecommons.org/licenses/by/4.0/
Accession Number: edsbas.C3BC16C3
Database: BASE