Skip to main content

Research Repository

Advanced Search

Selective Killing of BRCA2-Deficient Ovarian Cancer Cells via MRE11 Blockade

Alblihy, Adel; Ali, Reem; Algethami, Mashael; Ritchie, Alison A.; Shoqafi, Ahmed; Alqahtani, Shatha; Mesquita, Katia A.; Toss, Michael S.; Ordóñez-Morán, Paloma; Jeyapalan, Jennie N.; Dekker, Lodewijk; Salerno, Martina; Grabowska, Anna M.; Rakha, Emad A.; Mongan, Nigel P.; Madhusudan, Srinivasan

Selective Killing of BRCA2-Deficient Ovarian Cancer Cells via MRE11 Blockade Thumbnail


Authors

Adel Alblihy

Reem Ali

Mashael Algethami

Alison A. Ritchie

Ahmed Shoqafi

Shatha Alqahtani

Katia A. Mesquita

Michael S. Toss

Paloma Ordóñez-Morán

Jennie N. Jeyapalan

Martina Salerno

Anna M. Grabowska



Abstract

The MRE11 nuclease is essential during DNA damage recognition, homologous recombination, and replication. BRCA2 plays important roles during homologous recombination and replication. Here, we show that effecting an MRE11 blockade using a prototypical inhibitor (Mirin) induces synthetic lethality (SL) in BRCA2-deficient ovarian cancer cells, HeLa cells, and 3D spheroids compared to BRCA2-proficient controls. Increased cytotoxicity was associated with double-strand break accumulation, S-phase cell cycle arrest, and increased apoptosis. An in silico analysis revealed Mirin docking onto the active site of MRE11. While Mirin sensitises DT40 MRE11+/− cells to the Top1 poison SN-38, it does not sensitise nuclease-dead MRE11 cells to this compound confirming that Mirin specifically inhibits Mre11 nuclease activity. MRE11 knockdown reduced cell viability in BRCA2-deficient PEO1 cells but not in BRCA2-proficient PEO4 cells. In a Mirin-resistant model, we show the downregulation of 53BP1 and DNA repair upregulation, leading to resistance, including in in vivo xenograft models. In a clinical cohort of human ovarian tumours, low levels of BRCA2 expression with high levels of MRE11 co-expression were linked with worse progression-free survival (PFS) (p = 0.005) and overall survival (OS) (p = 0.001). We conclude that MRE11 is an attractive SL target, and the pharmaceutical development of MRE11 inhibitors for precision oncology therapeutics may be of clinical benefit.

Citation

Alblihy, A., Ali, R., Algethami, M., Ritchie, A. A., Shoqafi, A., Alqahtani, S., Mesquita, K. A., Toss, M. S., Ordóñez-Morán, P., Jeyapalan, J. N., Dekker, L., Salerno, M., Hartsuiker, E., Grabowska, A. M., Rakha, E. A., Mongan, N. P., & Madhusudan, S. (2023). Selective Killing of BRCA2-Deficient Ovarian Cancer Cells via MRE11 Blockade. International Journal of Molecular Sciences, 24(13), https://doi.org/10.3390/ijms241310966

Journal Article Type Article
Acceptance Date Jun 23, 2023
Online Publication Date Jun 30, 2023
Publication Date Jun 30, 2023
Deposit Date Apr 17, 2025
Publicly Available Date Apr 22, 2025
Journal International Journal of Molecular Sciences
Print ISSN 1661-6596
Electronic ISSN 1422-0067
Publisher MDPI
Peer Reviewed Peer Reviewed
Volume 24
Issue 13
DOI https://doi.org/10.3390/ijms241310966
Keywords BRCA2; MRE11; synthetic lethality
Public URL https://nottingham-repository.worktribe.com/output/22726146
Publisher URL https://www.mdpi.com/1422-0067/24/13/10966

Files

Selective Killing of BRCA2-Deficient Ovarian Cancer Cells via MRE11 Blockade (21.8 Mb)
PDF

Publisher Licence URL
https://creativecommons.org/licenses/by/4.0/

Copyright Statement
Copyright: © 2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https:// creativecommons.org/licenses/by/ 4.0/).





You might also like



Downloadable Citations