Bioengineered Tumor Organoids
- PMID: 32432209
- PMCID: PMC7236883
- DOI: 10.1016/j.cobme.2020.03.005
Bioengineered Tumor Organoids
Abstract
Recent advances in biofabrication technologies, such as cell culture systems, and biomaterials have led to the development of three-dimensional (3D) cell culture platforms, such as tumor organoids. Tumor organoids are more physiologically accurate to the in vivo system, which they are intended to model, compared with traditional 2D cancer cell culture systems. Tumor organoids can mimic pathological and physical characteristics of tumors as well as maintain genetic stability of the cancer cells. Furthermore tumor organoids have advantage over animal models, being made from human cells and easily controlled in the laboratory to attain the desired tissue characteristics. In this section, we describe general tumor organoid technologies, the importance of the tumor microenvironment (TME) in model culture systems, and the use of tumor organoids in drug development and precision medicine. Organoid technologies continue to develop rapidly for applications in academic, clinical, and pharmaceutical settings.
Keywords: 3D Cell Culture; Cancer Modelling; Extracellular Matrix; Tumor Microenvironment; Tumor Organoids.
Figures
References
-
-
Vlachogiannis G, et al., Patient-derived organoids model treatment response of metastatic gastrointestinal cancers. Science, 2018. 359(6378): p. 920–926.
** This recent review paper compares the responses to chemotheraputic agents Ex vivo in organoids and PDO-based orthotopic mouse tumor xenograph models with the responses of the patients in clinical trials and suggest that PDOs can recapiculate patient responses and could be implemented in personalized medicine.
-
-
- Forsythe S, Pu T, and Skardal A, Using organoid models to predict chemotherapy efficacy: the future of precision oncology? Expert Review of Precision Medicine and Drug Development, 2019. 4(6): p. 317–336.
-
- Balkwill FR, Capasso M, and Hagemann T, The tumor microenvironment at a glance. J Cell Sci, 2012. 125(Pt 23): p. 5591–6. - PubMed
Grants and funding
LinkOut - more resources
Full Text Sources