Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2025 Jan;21(1):211-225.
doi: 10.1007/s12015-024-10805-4. Epub 2024 Oct 21.

Patient-Derived Organoids: A Game-Changer in Personalized Cancer Medicine

Affiliations
Review

Patient-Derived Organoids: A Game-Changer in Personalized Cancer Medicine

Mohammad Hadi Abbasian et al. Stem Cell Rev Rep. 2025 Jan.

Abstract

Research on cancer therapies has benefited from predictive tools capable of simulating treatment response and other disease characteristics in a personalized manner, in particular three-dimensional cell culture models. Such models include tumor-derived spheroids, multicellular spheroids including organotypic multicellular spheroids, and tumor-derived organoids. Additionally, organoids can be grown from various cancer cell types, such as pluripotent stem cells and induced pluripotent stem cells, progenitor cells, and adult stem cells. Although patient-derived xenografts and genetically engineered mouse models replicate human disease in vivo, organoids are less expensive, less labor intensive, and less time-consuming, all-important aspects in high-throughput settings. Like in vivo models, organoids mimic the three-dimensional structure, cellular heterogeneity, and functions of primary tissues, with the advantage of representing the normal oxygen conditions of patient organs. In this review, we summarize the use of organoids in disease modeling, drug discovery, toxicity testing, and precision oncology. We also summarize the current clinical trials using organoids.

Keywords: Adult stem cells; Embryonic stem cells; Personalized cancer medicine; Pluripotent stem cells; Tumor-derived organoids.

PubMed Disclaimer

Conflict of interest statement

Declarations. Ethics Statement: Not applicable. Competing Interests: None.

References

    1. ME, J. F., Siegel, R. L., Isabelle Soerjomataram, M., Ahmedin, D., & Jemal (2024). Global cancer statistics 2022: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries.
    1. Sarhadi, V. K., & Armengol, G. (2022). Molecular biomarkers in cancer. Biomolecules, 12, 1021. - PubMed - PMC - DOI
    1. Bai, J. W., Qiu, S. Q., & Zhang, G. J. (2023). Molecular and functional imaging in cancer-targeted therapy: Current applications and future directions. Signal Transduction and Targeted Therapy, 8, 89. - PubMed - PMC - DOI
    1. Ishiguro, T., Ohata, H., Sato, A., Yamawaki, K., Enomoto, T., & Okamoto, K. (2017). Tumor-derived spheroids: Relevance to cancer stem cells and clinical applications. Cancer Science, 108, 283–289. - PubMed - PMC - DOI
    1. Kojima, N., Tao, F., Mihara, H., & Aoki, S. (2018). Methods for engineering of multicellular spheroids to reconstitute the liver tissue, stem cells and cancer in hepatology (pp. 145–158). Elsevier.

LinkOut - more resources