AI Article Synopsis

  • Immunotherapy aims to treat cancer by modifying the immune system, but traditional models fail to accurately represent the complex tumor microenvironment (TME).
  • Newer tumor mimic models, like patient-derived organoids, are essential for effectively evaluating immunotherapy treatments.
  • The review highlights current techniques for creating lung cancer organoid cultures that mimic TME, which can be used for preclinical testing of immunotherapy drugs tailored to individual patients.

Article Abstract

In immunotherapy, the immune system is modulated in order to treat cancer. Traditional two dimensional models and animal models are insufficient to simulate the complex tumor microenvironment (TME) in the original tumor. As tumor immunotherapy involves the immune system, additional tumor mimic models, such as patient-derived organoids, are required for the evaluation of the efficacy of immunotherapy. Furthermore, non-tumor components and host tumor cells in the TME may interact to promote cancer incidence, progression, drug resistance and metastasis. It is possible to produce organoid models for lung cancer by retaining endogenous stromal components (e.g., multiple immune cell types), supplying cancer-associated fibroblasts and exogenous immune cells, constructing tumor vasculature and adding other biological or chemical components that emulate the TME. Therefore, the lung cancer organoid culture platform may facilitate preclinical testing of immunotherapy drugs for lung cancer by mimicking immunotherapy responses. The present review summarizes current lung cancer organoid culture methods for TME modeling and discusses the use of lung cancer-derived organoids for the detection of lung cancer immunotherapy and individualized cancer immunotherapy.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10561155PMC
http://dx.doi.org/10.3892/ol.2023.14071DOI Listing

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