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- W4313436043 abstract "Ovarian cancer (OC) is the leading cause of death from gynecological malignancies. Despite great advances in treatment strategies, therapeutic resistance and the gap between preclinical data and actual clinical efficacy justify the necessity of developing novel models for investigating OC. Organoids represent revolutionary three-dimensional cell culture models, deriving from stem cells and reflecting the primary tissue's biology and pathology. The aim of the current review is to study the current status of mouse- and patient-derived organoids, as well as their potential to model carcinogenesis and perform drug screenings for OC. Herein, we describe the role of organoids in the assessment of high-grade serous OC (HGSOC) cells-of-origin, illustrate their use as promising preclinical OC models and highlight the advantages of organoid technology in terms of disease modelling and drug sensitivity testing." @default.
- W4313436043 created "2023-01-06" @default.
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- W4313436043 creator A5049664524 @default.
- W4313436043 creator A5088488734 @default.
- W4313436043 date "2022-12-20" @default.
- W4313436043 modified "2023-10-16" @default.
- W4313436043 title "Patient-Derived Organoids: The Beginning of a New Era in Ovarian Cancer Disease Modeling and Drug Sensitivity Testing" @default.
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- W4313436043 doi "https://doi.org/10.3390/biomedicines11010001" @default.
- W4313436043 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/36672509" @default.
- W4313436043 hasPublicationYear "2022" @default.
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