4.8 Review

Cancer modeling meets human organoid technology

Journal

SCIENCE
Volume 364, Issue 6444, Pages 952-955

Publisher

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.aaw6985

Keywords

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Funding

  1. Lustgarten Foundation
  2. Cold Spring Harbor Laboratory Association
  3. Cold Spring Harbor Laboratory and Northwell Health Affiliation
  4. National Institutes of Health [NIH 5P30CA45508-29, 5P50CA101955-07, P20CA192996-03, 1U10CA180944-04, U01CA210240-01A1, 1R01CA188134-01, 1R01CA190092-04]
  5. [EU-ERC-670133]

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Organoids are microscopic self-organizing, three-dimensional structures that are grown from stem cells in vitro. They recapitulate many structural and functional aspects of their in vivo counterpart organs. This versatile technology has led to the development of many novel human cancer models. It is now possible to create indefinitely expanding organoids starting from tumor tissue of individuals suffering from a range of carcinomas. Alternatively, CRISPR-based gene modification allows the engineering of organoid models of cancer through the introduction of any combination of cancer gene alterations to normal organoids. When combined with immune cells and fibroblasts, tumor organoids become models for the cancer microenvironment enabling immune-oncology applications. Emerging evidence indicates that organoids can be used to accurately predict drug responses in a personalized treatment setting. Here, we review the current state and future prospects of the rapidly evolving tumor organoid field.

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