Table 6.
3D Models | |
---|---|
Pros | Cons |
Modeling of difficult to access tissues | Many non-uniform protocols |
Monitoring developmental stages | Many different materials |
Diversity of cell types | Great variability of results |
Interaction between cell types | Insufficient vascularization |
Identical genetic background | Interaction |
Possibility of genetic manipulation | |
Easy handling | |
Spatial organization | |
Tailor-made microenvironment |