Maria Lopez-Cavestany,Olivia A. Wright,Noah T. Reckhorn,Alexandria T. Carter,Kalana W. Jayawardana,Tin Nguyen,Dayrl P. Briggs,Dmitry S. Koktysh,Alberto Esteban‐Linares,Deyu Li,Michael R. King
出处
期刊:ACS Nano [American Chemical Society] 日期:2024-08-16卷期号:18 (34): 23637-23654被引量:1
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.