Table 1.
Origin of organoid | Availability | Protocols | Differentiation potential |
Potential
use as ATMP* |
Cancer
organoid models |
Utility in
cancer immunology research |
Potential
for use in infectious diseases |
Genome
editing |
Organ-on
chip studies |
Potential biobanks |
Challenges
ahead in 2021 |
---|---|---|---|---|---|---|---|---|---|---|---|
Adult-tissue-derived | Requires tissue and biopsy | Relatively easy | Depends on the type of organs and stem cells | Limited | High potential | Yes, TME** with immune components are present | Limited (Requires tissue sampling) | Limited | Yes | Yes | Improved differentiation protocols |
Ability to expand | |||||||||||
iPSC-derived | Readily available from iPSC | Complex and multistep procedures | Theoretically unlimited towards any tissue | High potential | High potential but TME absent. | TME components are not reproduced in a single step | High Potential | High potential | Yes | Yes | Simplified differentiation protocols |
Interest in hereditary cancer studies | Adequate vascularization and innervation |
Advances therapeutic medicinal product.
Tumor micro-environment.