TY - JOUR
T1 - Superhydrophobic Array Devices for the Enhanced Formation of 3D Cancer Models
AU - Lopez-Cavestany, Maria
AU - Wright, Olivia A.
AU - Reckhorn, Noah T.
AU - Carter, Alexandria T.
AU - Jayawardana, Kalana
AU - Nguyen, Tin
AU - Briggs, Dayrl P.
AU - Koktysh, Dmitry S.
AU - Esteban Linares, Alberto
AU - Li, Deyu
AU - King, Michael R.
N1 - Publisher Copyright:
© 2024 The Authors. Published by American Chemical Society.
PY - 2024/8/27
Y1 - 2024/8/27
N2 - 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.
AB - 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.
KW - 3D mammalian cell cultures
KW - biological-material interfaces
KW - cancer
KW - microfabrication
KW - nanostructured surfaces
KW - superhydrophobicity
UR - http://www.scopus.com/inward/record.url?scp=85201508921&partnerID=8YFLogxK
U2 - 10.1021/acsnano.4c08132
DO - 10.1021/acsnano.4c08132
M3 - Article
C2 - 39150223
AN - SCOPUS:85201508921
SN - 1936-0851
VL - 18
SP - 23637
EP - 23654
JO - ACS Nano
JF - ACS Nano
IS - 34
ER -