ArticleiScience2025
Organoid platinum-resistance model identifies KRT17 as a biomarker of targeted therapy in ovarian cancer.
Article in iScience, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
1 citing paper in PubMed.
- Organoids and AI-integrated models in ovarian cancer research: the future of personalized therapy.Frontiers in oncology · 2026Review
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20 authors.
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Abstract
Variable responses to platinum chemotherapy and the emergence of resistant disease drive high mortality in high-grade serous ovarian cancer (HGSOC). To study resistance mechanisms, we developed the organoid drug resistance assay (ODR-test) with patient-derived organoids from our ovarian cancer biobank and identified sustained phenotypic reprogramming and cellular plasticity of organoids under carboplatin pressure as a conserved mechanism irrespective of the basal resistance level. Transcriptional and proteomic analyses revealed changes in cell adhesion and differentiation as adaptive responses that lead to an increase in resistance. We identified Keratin 17 (KRT17) as a mediator of platinum resistance and validated its function by CRISPR-Cas9 and overexpression. Additionally, we found that KRT17 expression status (K-score) is a significant negative prognostic histopathological biomarker in a large cohort ( Video abstract:
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