Adel Alblihy
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
Authors
Reem Ali
Mashael Algethami
Alison A. Ritchie
Ahmed Shoqafi
Shatha Alqahtani
Katia A. Mesquita
Michael S. Toss
Paloma Ordóñez-Morán
Jennie N. Jeyapalan
Dr LODEWIJK DEKKER LODEWIJK.DEKKER@NOTTINGHAM.AC.UK
ASSOCIATE PROFESSOR
Martina Salerno
Anna M. Grabowska
Professor EMAD RAKHA Emad.Rakha@nottingham.ac.uk
PROFESSOR OF BREAST CANCER PATHOLOGY
Professor Nigel Mongan nigel.mongan@nottingham.ac.uk
ASSOCIATE PRO-VICE CHANCELLORGLOBAL ENGAGEMENT
Professor SRINIVASAN MADHUSUDAN srinivasan.madhusudan@nottingham.ac.uk
PROFESSOR OF MEDICAL ONCOLOGY
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 |
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Selective Killing of BRCA2-Deficient Ovarian Cancer Cells via MRE11 Blockade
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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/).
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