Superhydrophobic Array Devices for the Enhanced Formation of 3D Cancer Models.
Maria Lopez-CavestanyOlivia A WrightNoah T ReckhornAlexandria T CarterKalana JayawardanaTin NguyenDayrl P BriggsDmitry S KoktyshAlberto Esteban-LinaresDeyu LiMichael R KingPublished in: ACS nano (2024)
During the metastatic cascade, cancer cells travel through the bloodstream as circulating tumor cells (CTCs) to a secondary site. Clustered CTCs have greater shear stress and treatment resistance, yet their biology remains poorly understood. We therefore engineered a tunable superhydrophobic array device (SHArD). The SHArD-C was applied to culture a clinically relevant model of CTC clusters. Using our device, we cultured a model of cancer cell aggregates of various sizes with immortalized cancer cell lines. These exhibited higher E-cadherin expression and are significantly more capable of surviving high fluid shear stress-related forces compared to single cells and model clusters grown using the control method, helping to explain why clustering may provide a metastatic advantage. Additionally, the SHArD-S, when compared with the AggreWell 800 method, provides a more consistent spheroid-forming device culturing reproducible sizes of spheroids for multiple cancer cell lines. Overall, we designed, fabricated, and validated an easily tunable engineered device which grows physiologically relevant three-dimensional (3D) cancer models containing tens to thousands of cells.
Keyphrases
- circulating tumor cells
- papillary thyroid
- squamous cell
- small cell lung cancer
- squamous cell carcinoma
- high resolution
- high throughput
- cell cycle arrest
- poor prognosis
- endothelial cells
- escherichia coli
- young adults
- pi k akt
- replacement therapy
- long non coding rna
- high density
- gram negative
- infectious diseases
- cell free