105P Discovery of potent and selective PKMYT1 inhibitors

Methods:We employed a tiered experimental approach encompassing cell line panels, isogenic Rb1 manipulated cell line systems, and patient derived xenograft models, stratified by Rb1 status. Results:We demonstrate that co-inhibition of ATR (RP-3500) and PKMYT1 (RP-6306) induces synthetic lethality in Rb1-deficient breast cancers by disrupting both S/G2 and G2/M checkpoints.This leads to replication stress, premature mitotic entry, and accumulation of DNA damage.In vitro, Rb1-deficient breast cancer cells exhibited marked apoptosis and loss of clonogenic survival, whereas Rb1-proficient models remained resistant to combination treatment.Genetic manipulation confirmed this dependency: Rb1 knockdown sensitized resistant models, whereas re-expression conferred protection.In vivo, patient-derived xenograft (PDX) models recapitulated these findings.Rb1-deficient tumors regressed following ATR/PKMYT1 co-inhibition, whereas Rb1-proficient tumors showed only modest responses.Combination therapy was well tolerated without weight loss or measurable toxicity.Biomarker analysis revealed increased H2AX and reduced Ki67 staining exclusively in Rb1-deficient PDX models, underscoring the specificity of this response.Mechanistically, Rb1 loss impaired double-strand DNA repair by attenuating homologous recombination and non-homologous end joining, leading to replication fork collapse, chromosomal instability, and mitotic catastrophe.Proteogenomic analysis identified JNK/p38 stress response pathway activation as a key driver of apoptosis following ATR/PKMYT1 inhibition in Rb1-deficient cells.Clinically, retrospective analysis of stage IV breast cancer datasets revealed that Rb1-low tumors display reduced DNA repair pathway activity in triple-negative and CDK4/6 inhibitor-resistant luminal breast cancers.Conclusions: These results identify Rb1 loss as a predictive biomarker for ATR/ PKMYT1-targeted therapy, offering a potential precision treatment strategy for advanced breast cancers.

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Publication Details

Journal
ESMO Open
Published
2026-04-01
DOI
https://doi.org/10.1016/j.esmoop.2026.106247
Primary Topic
PI3K/AKT/mTOR signaling in cancer
Type
article
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article

105P Discovery of potent and selective PKMYT1 inhibitors

Matthew J. Walters, Lunda Shen, Jeremy Fournier, Manmohan R. Leleti et al.
ESMO Open
PI3K/AKT/mTOR signaling in cancer
article

105P Discovery of potent and selective PKMYT1 inhibitors

Matthew J. Walters, Lunda Shen, Jeremy Fournier, Manmohan R. Leleti, Sandra Hodge, Natalie Hill, S. Bhowmik, E. Fernandez-Salas, H. Vishwa Sai, J. Zhu, P. Nareddy, E. Rumpf, M. Yadav, C. Ashar, S. Paladugu
article en

Abstract

Methods:We employed a tiered experimental approach encompassing cell line panels, isogenic Rb1 manipulated cell line systems, and patient derived xenograft models, stratified by Rb1 status. Results:We demonstrate that co-inhibition of ATR (RP-3500) and PKMYT1 (RP-6306) induces synthetic lethality in Rb1-deficient breast cancers by disrupting both S/G2 and G2/M checkpoints.This leads to replication stress, premature mitotic entry, and accumulation of DNA damage.In vitro, Rb1-deficient breast cancer cells exhibited marked apoptosis and loss of clonogenic survival, whereas Rb1-proficient models remained resistant to combination treatment.Genetic manipulation confirmed this dependency: Rb1 knockdown sensitized resistant models, whereas re-expression conferred protection.In vivo, patient-derived xenograft (PDX) models recapitulated these findings.Rb1-deficient tumors regressed following ATR/PKMYT1 co-inhibition, whereas Rb1-proficient tumors showed only modest responses.Combination therapy was well tolerated without weight loss or measurable toxicity.Biomarker analysis revealed increased H2AX and reduced Ki67 staining exclusively in Rb1-deficient PDX models, underscoring the specificity of this response.Mechanistically, Rb1 loss impaired double-strand DNA repair by attenuating homologous recombination and non-homologous end joining, leading to replication fork collapse, chromosomal instability, and mitotic catastrophe.Proteogenomic analysis identified JNK/p38 stress response pathway activation as a key driver of apoptosis following ATR/PKMYT1 inhibition in Rb1-deficient cells.Clinically, retrospective analysis of stage IV breast cancer datasets revealed that Rb1-low tumors display reduced DNA repair pathway activity in triple-negative and CDK4/6 inhibitor-resistant luminal breast cancers.Conclusions: These results identify Rb1 loss as a predictive biomarker for ATR/ PKMYT1-targeted therapy, offering a potential precision treatment strategy for advanced breast cancers.

ESMO OpenVol. 11
Profectus Biosciences (United States) (US), Pulse Biosciences (United States) (US), Arcadia Biosciences (United States) (US)
Zero hunger
Openalex Percentile: Top 10%
PI3K/AKT/mTOR signaling in cancer
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