Acoustic Bioprinting of Patient-Derived Organoids for Predicting Cancer Therapy Responses

Cancer models, which are biologically representative of patient tumors, can predict the treatment responses and help determine the most appropriate cancer treatment for individual patients. Here, a point-of-care testing system called acoustically bioprinted patient-derived microtissues (PDMs) that can model cancer invasion and predict treatment response in individual patients with colorectal cancer (CRC), is reported. The PDMs are composed of patient-derived colorectal tumors and healthy organoids which can be precisely arranged by acoustic bioprinting approach for recapulating primary tissue's architecture. Particularly, these tumor organoids can be efficiently generated and can apprehend histological, genomic, and phenotypical characteristics of primary tumors. Consequently, these PDMs allow physiologically relevant in vitro drug (5-fluorouracil) screens, thus predicting the paired patient's responses to chemotherapy. A correlation between organoid invasion speed and normalized spreading speed of the paired patients is further established. It provides a quantitative indicator to help doctors make better decisions on ultimate anus-preserving operation for extremely low CRC patients. Thus, by combing acoustic bioprinting and organoid cultures, this method may open an avenue to establish complex 3D tissue models for precision and personalized medicine.

Automated summary

A testing system called acoustically bioprinted patient-derived microtissues (PDMs) is reported, which can model cancer invasion and predict treatment response in individual patients with colorectal cancer. This method allows the precise arrangement of patient-derived colorectal tumors and healthy organoids, recapitulating the architecture of the primary tissue. It also enables the prediction of patients' response to chemotherapy and provides a quantitative indicator for better decision-making in treatment.