A vascularized breast cancer spheroid platform for the ranked evaluation of tumor microenvironment-targeted drugs by light sheet fluorescence microscopy.
David AscheidMagdalena BaumannJürgen PinneckerMike FriedrichDaniel Szi-MartonCornelia MedvedMaja BundaloVanessa OrtmannAsli ÖztürkRajender NandigamaKatherina HemmenSüleymann ErgünAlma ZerneckeMatthias HirthKatrin G HeinzeErik HenkePublished in: Nature communications (2024)
Targeting the supportive tumor microenvironment (TME) is an approach of high interest in cancer drug development. However, assessing TME-targeted drug candidates presents a unique set of challenges. We develop a comprehensive screening platform that allows monitoring, quantifying, and ranking drug-induced effects in self-organizing, vascularized tumor spheroids (VTSs). The confrontation of four human-derived cell populations makes it possible to recreate and study complex changes in TME composition and cell-cell interaction. The platform is modular and adaptable for tumor entity or genetic manipulation. Treatment effects are recorded by light sheet fluorescence microscopy and translated by an advanced image analysis routine in processable multi-parametric datasets. The system proved to be robust, with strong interassay reliability. We demonstrate the platform's utility for evaluating TME-targeted antifibrotic and antiangiogenic drugs side-by-side. The platform's output enabled the differential evaluation of even closely related drug candidates according to projected therapeutic needs.
Keyphrases
- drug induced
- high throughput
- liver injury
- single cell
- single molecule
- cancer therapy
- cell therapy
- high resolution
- endothelial cells
- rna seq
- adverse drug
- emergency department
- climate change
- stem cells
- gene expression
- clinical practice
- squamous cell carcinoma
- papillary thyroid
- mesenchymal stem cells
- mass spectrometry
- squamous cell
- electronic health record
- induced pluripotent stem cells