Retain the 3D architecture of the original tumor, including stromal and immune cell compartments. |
Lack of vascularization does not permit long-term culture |
Quick, easy, and relatively inexpensive to generate and culture |
Cannot currently be frozen or biobanked |
Allow studies on the immunobiology of tumors |
Any experiments need to fit within the short-term culture timeframe of ~one week |
Drug screening of immunotherapeutic agents is possible |
Low throughput platform with no direct multi-omics possible |
Permit several assay applications following culture (IHC, flow cytometry, confocal, microscopy, sequencing and supernatant readouts) |
Inter- and intra-tumoral heterogeneity observed |
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Organ/tumor-specific transcriptional changes observed following slicing |