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Abstract 5697: Targeting PARP inhibitor resistance with Polθ inhibitors

Authors :
Diana Zatreanu
Helen Robinson
Omar Alkhatib
Marie Boursier
Harry Finch
Lerin Geo
Diego Grande
Vera Grinkevich
Robert Heald
Sophie Langdon
Jayesh Majithiya
Claire McWhirter
Niall Martin
Shaun Moore
Joana Neves
Eeson Rajendra
Marco Ranzani
Theresia Schaedler
Martin Stockley
Kimberley Wiggins
Rachel Brough
Sandhya Sridhar
Aditi Gulati
Nan Shao
Luted Badder
Daniela Novo
Eleanor Knight
Rebecca Marlow
Syed Haider
Elsa Callen
Graeme Hewitt
Joost Schimmel
Remko Prevo
Christina Alli
Amanda Ferdinand
Cameron Bell
Peter Blencowe
Chris Bot
Mathew Calder
Mark Charles
Jayne Curry
Tennyson Ekwuru
Andre Nussenzweig
Marcel Tijsterman
Andrew N. Tutt
Simon Boulton
Geoff Higgins
Stephen J. Pettitt
Graeme C. Smith
Christopher J. Lord
Source :
Cancer Research. 82:5697-5697
Publication Year :
2022
Publisher :
American Association for Cancer Research (AACR), 2022.

Abstract

To target DNA repair vulnerabilities in cancer, we discovered nanomolar potent, selective, low molecular weight (MW), allosteric inhibitors of the polymerase function of DNA polymerase Polθ, including ART558. ART558 inhibits the major Polθ-mediated DNA repair process, Theta-Mediated End Joining (TMEJ), without targeting Non-Homologous End Joining. Moreover, we show that exposure to ART558 can elicit DNA damage and synthetic lethality in BRCA1- or BRCA2-mutant tumor cells and enhances the effects of a PARP inhibitor. Genetic perturbation screening revealed that defects in the 53BP1/Shieldin complex, which are a cause of PARP inhibitor resistance, result in in vitro and in vivo sensitivity to Polθ polymerase inhibitors. Mechanistically, ART558 increases biomarkers of single-stranded DNA and synthetic lethality in 53BP1-defective cells. The inhibition of DNA nucleases that promote end-resection, such as Exo1 or Blm-Dna2 reversed these effects, implicating these in the synthetic lethal mechanism-of-action. Taken together, these observations describe a drug class that elicits BRCA-gene synthetic lethality and PARP inhibitor synergy, as well as targeting a biomarker-defined mechanism of PARPi-resistance. Citation Format: Diana Zatreanu, Helen Robinson, Omar Alkhatib, Marie Boursier, Harry Finch, Lerin Geo, Diego Grande, Vera Grinkevich, Robert Heald, Sophie Langdon, Jayesh Majithiya, Claire McWhirter, Niall Martin, Shaun Moore, Joana Neves, Eeson Rajendra, Marco Ranzani, Theresia Schaedler, Martin Stockley, Kimberley Wiggins, Rachel Brough, Sandhya Sridhar, Aditi Gulati, Nan Shao, Luted Badder, Daniela Novo, Eleanor Knight, Rebecca Marlow, Syed Haider, Elsa Callen, Graeme Hewitt, Joost Schimmel, Remko Prevo, Christina Alli, Amanda Ferdinand, Cameron Bell, Peter Blencowe, Chris Bot, Mathew Calder, Mark Charles, Jayne Curry, Tennyson Ekwuru, Andre Nussenzweig, Marcel Tijsterman, Andrew N. Tutt, Simon Boulton, Geoff Higgins, Stephen J. Pettitt, Graeme C. Smith, Christopher J. Lord. Targeting PARP inhibitor resistance with Polθ inhibitors [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2022; 2022 Apr 8-13. Philadelphia (PA): AACR; Cancer Res 2022;82(12_Suppl):Abstract nr 5697.

Subjects

Subjects :
Cancer Research
Oncology

Details

ISSN :
15387445
Volume :
82
Database :
OpenAIRE
Journal :
Cancer Research
Accession number :
edsair.doi...........ef0d9d73e0b3ce9af06ce913425ebd3e
Full Text :
https://doi.org/10.1158/1538-7445.am2022-5697