Tumor organoids as personalized preclinical models
The recent discovery of many different subtypes and tumor entities also revealed a potential problem for finding more efficient treatments: not all tumors are alike!
Therefore, we need many new and well-characterized preclinical models representing all the different molecular subtypes to test new therapeutic strategies. Together with other groups at the Princess Máxima Center, we are generating brain tumor organoids (BTOs). These are 3D cultures of tumors from our patients. This BTO approach has advantages over other approaches. Compared to normal 2D cell culture techniques, these BTOs better represent the original tumor and its heterogeneity. It also allows a more high-throughput approach than using tumor xenografts in mice. We aim to generate a living biobank of patient derived BTOs. We will use these organoids in drug screens to investigate whether the tumor might be sensitive for FDA approved drugs and new drug candidates.
Tumors always exist within the context healthy brain cells. To study this and to better understand the relationship between tumor cells and the surrounding normal brain tissue, we will combine tumor organoids with normal brain organoids. These brain organoid – tumor co-cultures enable us to screen for drugs that specifically target the tumor cells and not the normal brain cells. We will also us this model to study how tumor cells migrate and metastasize.