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Targeting Mre11 overcomes platinum resistance and induces synthetic lethality in XRCC1 deficient epithelial ovarian cancers

Alblihy, Adel; Ali, Reem; Algethami, Mashael; Shoqafi, Ahmed; Toss, Michael S.; Brownlie, Juliette; Tatum, Natalie J.; Hickson, Ian; Moran, Paloma Ordonez; Grabowska, Anna; Jeyapalan, Jennie N.; Mongan, Nigel P.; Rakha, Emad A.; Madhusudan, Srinivasan

Targeting Mre11 overcomes platinum resistance and induces synthetic lethality in XRCC1 deficient epithelial ovarian cancers Thumbnail


Authors

Adel Alblihy

Reem Ali

Mashael Algethami

Ahmed Shoqafi

Michael S. Toss

Juliette Brownlie

Natalie J. Tatum

Ian Hickson

Anna Grabowska

Jennie N. Jeyapalan

NIGEL MONGAN nigel.mongan@nottingham.ac.uk
Associate Pro-Vice Chancellorglobal Engagement

Emad A. Rakha



Abstract

Platinum resistance is a clinical challenge in ovarian cancer. Platinating agents induce DNA damage which activate Mre11 nuclease directed DNA damage signalling and response (DDR). Upregulation of DDR may promote chemotherapy resistance. Here we have comprehensively evaluated Mre11 in epithelial ovarian cancers. In clinical cohort that received platinum- based chemotherapy (n = 331), Mre11 protein overexpression was associated with aggressive phenotype and poor progression free survival (PFS) (p = 0.002). In the ovarian cancer genome atlas (TCGA) cohort (n = 498), Mre11 gene amplification was observed in a subset of serous tumours (5%) which correlated highly with Mre11 mRNA levels (p < 0.0001). Altered Mre11 levels was linked with genome wide alterations that can influence platinum sensitivity. At the transcriptomic level (n = 1259), Mre11 overexpression was associated with poor PFS (p = 0.003). ROC analysis showed an area under the curve (AUC) of 0.642 for response to platinum-based chemotherapy. Pre-clinically, Mre11 depletion by gene knock down or blockade by small molecule inhibitor (Mirin) reversed platinum resistance in ovarian cancer cells and in 3D spheroid models. Importantly, Mre11 inhibition was synthetically lethal in platinum sensitive XRCC1 deficient ovarian cancer cells and 3D-spheroids. Selective cytotoxicity was associated with DNA double strand break (DSB) accumulation, S-phase cell cycle arrest and increased apoptosis. We conclude that pharmaceutical development of Mre11 inhibitors is a viable clinical strategy for platinum sensitization and synthetic lethality in ovarian cancer.

Citation

Alblihy, A., Ali, R., Algethami, M., Shoqafi, A., Toss, M. S., Brownlie, J., …Madhusudan, S. (2022). Targeting Mre11 overcomes platinum resistance and induces synthetic lethality in XRCC1 deficient epithelial ovarian cancers. npj Precision Oncology, 6(1), https://doi.org/10.1038/s41698-022-00298-0

Journal Article Type Article
Acceptance Date Jul 4, 2022
Online Publication Date Jul 19, 2022
Publication Date 2022-12
Deposit Date Apr 9, 2023
Publicly Available Date Apr 20, 2023
Journal npj Precision Oncology
Print ISSN 2397-768X
Publisher Nature Research
Peer Reviewed Peer Reviewed
Volume 6
Issue 1
DOI https://doi.org/10.1038/s41698-022-00298-0
Keywords Cancer Research; Oncology
Public URL https://nottingham-repository.worktribe.com/output/9093495
Additional Information Received: 12 October 2021; Accepted: 4 July 2022; First Online: 19 July 2022; : The authors declare no competing interests.

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