Skip to main content
. Author manuscript; available in PMC: 2022 Jul 1.
Published in final edited form as: Cancer Lett. 2021 Apr 7;509:39–52. doi: 10.1016/j.canlet.2021.03.031

Table 1.

Use of 3D Organoids to Model Esophageal Cancer Development and Progression

Advantages

Recapitulation of histology of primary tissue of origin (normal, dysplastic, cancer)
Recapitulation of genetic and epigenetic signature of original tissue/tumor
Recapitulation of tumor clonal heterogeneity
Evaluation of individual clones and tumor initiating cells
Long-term culture and passaging
Biobanking of patient samples across institutions
Conversion to 2D culture
High-throughput drug screening
High-throughput gene editing
Personalized medicine using PDOs

Limitations

Lack diverse cell types and microenvironment of original tumors
Unknown genetic and epigenetic stability over multiple passages
Clonal drift over multiple passages