Multiplexed drug testing of tumor slices using a microfluidic platform.
Lisa F HorowitzA D RodriguezZ Dereli-KorkutR LinK CastroAndrei M MikheevRaymond J MonnatAlbert FolchRobert C RostomilyPublished in: NPJ precision oncology (2020)
Current methods to assess the drug response of individual human cancers are often inaccurate, costly, or slow. Functional approaches that rapidly and directly assess the response of patient cancer tissue to drugs or small molecules offer a promising way to improve drug testing, and have the potential to identify the best therapy for individual patients. We developed a digitally manufactured microfluidic platform for multiplexed drug testing of intact cancer slice cultures, and demonstrate the use of this platform to evaluate drug responses in slice cultures from human glioma xenografts and patient tumor biopsies. This approach retains much of the tissue microenvironment and can provide results rapidly enough, within days of surgery, to guide the choice of effective initial therapies. Our results establish a useful preclinical platform for cancer drug testing and development with the potential to improve cancer personalized medicine.
Keyphrases
- papillary thyroid
- high throughput
- squamous cell
- endothelial cells
- single cell
- stem cells
- adverse drug
- lymph node metastasis
- end stage renal disease
- minimally invasive
- ejection fraction
- newly diagnosed
- squamous cell carcinoma
- acute coronary syndrome
- computed tomography
- magnetic resonance
- young adults
- peritoneal dialysis
- climate change
- cell therapy
- image quality