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

  • Hui Chen
  • , Zhuhao Wu
  • , Zhiyi Gong
  • , Yu Xia
  • , Juan Li
  • , Liang Du
  • , Yuanzheng Zhang
  • , Xiangyang Gao
  • , Zhou Fan
  • , Hang Hu
  • , Qun Qian
  • , Zhao Ding
  • , Shishang Guo

Research output: Contribution to journal › Article › peer-review

69 Scopus citations

Abstract

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.

Original languageEnglish
Article number2102784
JournalAdvanced healthcare materials
Volume11
Issue number13
DOIs
StatePublished - 6 Jul 2022
Externally publishedYes

Keywords

  • acoustic printing
  • personalized treatment
  • treatment prediction
  • tumor invasion
  • tumor organoids

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