Abstract 73: Molecular characterization of senescence induced by PARPi in preclinical xenograft mouse models of ovarian cancer

Abstract Introduction: Ovarian cancer (OC) is amongst the most lethal cancers in Canada. High-grade serous ovarian cancer (HGSC) usually responds to initial therapy, however resistance to drugs often develops over time. We have described a new two-step OC combo-therapy: 1st, a PARP inhibitor is used to induce a senescence proliferation arrest in cancer cells followed by, 2nd, the induction of senolysis in senescent cancer cells using the Bcl-2 family inhibitor ABT263, which redirects senescent cells towards apoptosis. Our hypothesis is that therapy-induced senescence (TIS) could be beneficial in the clinic, but questions remain on its exact function in this context. Our objective is to characterize the spatiotemporal evolution of senescence during OC treatment using xenograft mouse models to define the senescence peak in tissues and optimize the targeting of senolysis approaches. Methods-results: We generate a tumor biobank consisting of OV1946, OV4453, TOV21G and MDAMB231 preclinical xenograft models treated with combinations of the PARP inhibitor Olaparib and ABT263. In all models, PARPi-ABT263 resulted in a significant reduction in tumor growth compared to each drug alone. To explore spatiotemporal cell fate decisions including senescence, a time course analysis was performed by gene expression analysis, SA-βgal staining and COMET multiplexing. COMET is an immunofluorescence technology that allows up to 40 molecular biomarkers (vasculature, epithelium, senescence phenotypes, DNA damage response) at single-cell resolution on paraffin embedded tumors. Conclusion: We propose that characterizing the cell fate decisions within the tumor including senescence can be used to improve drug administration patterns in combo therapies and reduce resistance. For example, this should refine targets and timing to improve chemotherapies that aim to manipulate senescence. Citation Format: Sarah Saoudaoui, Nicolas Malaquin, Isabelle Clément, Tibila Kientega, Erwan Goy, Kim Leclerc-Desaulniers, Anne Marie Mes-Masson, Francis Rodier. Molecular characterization of senescence induced by PARPi in preclinical xenograft mouse models of ovarian cancer [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2025; Part 1 (Regular Abstracts); 2025 Apr 25-30; Chicago, IL. Philadelphia (PA): AACR; Cancer Res 2025;85(8_Suppl_1):Abstract nr 73.

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Journal
Cancer Research
Published
2025-04-21
DOI
https://doi.org/10.1158/1538-7445.am2025-73
Primary Topic
PARP inhibition in cancer therapy
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article
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article

Abstract 73: Molecular characterization of senescence induced by PARPi in preclinical xenograft mouse models of ovarian cancer

Kim Leclerc-Desaulniers, I Clément, Erwan Goy, Nicolas Malaquin et al.
Cancer Research
PARP inhibition in cancer therapy
article

Abstract 73: Molecular characterization of senescence induced by PARPi in preclinical xenograft mouse models of ovarian cancer

Kim Leclerc-Desaulniers, I Clément, Erwan Goy, Nicolas Malaquin, Sarah Saoudaoui, Anne‐Marie Mes‐Masson, Françis Rodier, Tibila Kientega
article en

Abstract

Abstract Introduction: Ovarian cancer (OC) is amongst the most lethal cancers in Canada. High-grade serous ovarian cancer (HGSC) usually responds to initial therapy, however resistance to drugs often develops over time. We have described a new two-step OC combo-therapy: 1st, a PARP inhibitor is used to induce a senescence proliferation arrest in cancer cells followed by, 2nd, the induction of senolysis in senescent cancer cells using the Bcl-2 family inhibitor ABT263, which redirects senescent cells towards apoptosis. Our hypothesis is that therapy-induced senescence (TIS) could be beneficial in the clinic, but questions remain on its exact function in this context. Our objective is to characterize the spatiotemporal evolution of senescence during OC treatment using xenograft mouse models to define the senescence peak in tissues and optimize the targeting of senolysis approaches. Methods-results: We generate a tumor biobank consisting of OV1946, OV4453, TOV21G and MDAMB231 preclinical xenograft models treated with combinations of the PARP inhibitor Olaparib and ABT263. In all models, PARPi-ABT263 resulted in a significant reduction in tumor growth compared to each drug alone. To explore spatiotemporal cell fate decisions including senescence, a time course analysis was performed by gene expression analysis, SA-βgal staining and COMET multiplexing. COMET is an immunofluorescence technology that allows up to 40 molecular biomarkers (vasculature, epithelium, senescence phenotypes, DNA damage response) at single-cell resolution on paraffin embedded tumors. Conclusion: We propose that characterizing the cell fate decisions within the tumor including senescence can be used to improve drug administration patterns in combo therapies and reduce resistance. For example, this should refine targets and timing to improve chemotherapies that aim to manipulate senescence. Citation Format: Sarah Saoudaoui, Nicolas Malaquin, Isabelle Clément, Tibila Kientega, Erwan Goy, Kim Leclerc-Desaulniers, Anne Marie Mes-Masson, Francis Rodier. Molecular characterization of senescence induced by PARPi in preclinical xenograft mouse models of ovarian cancer [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2025; Part 1 (Regular Abstracts); 2025 Apr 25-30; Chicago, IL. Philadelphia (PA): AACR; Cancer Res 2025;85(8_Suppl_1):Abstract nr 73.

Cancer ResearchVol. 85(8_Supplement_1)
Centre Hospitalier de l’Université de Montréal (CA)
Openalex Percentile: Top 87%
PARP inhibition in cancer therapy
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