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Open AccessArticle

Simple In-House Fabrication of Microwells for Generating Uniform Hepatic Multicellular Cancer Aggregates and Discovering Novel Therapeutics

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Department of Biomedical Engineering, National Cheng Kung University, Tainan 70101, Taiwan
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Department of Chemistry, National Cheng Kung University, Tainan 70101, Taiwan
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Medical Device Innovation Center, National Cheng Kung University, Tainan 70101, Taiwan
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Center for Micro/Nano Technology Research, National Cheng Kung University, Tainan 70101, Taiwan
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Department of Mechanical Engineering, National Cheng Kung University, Tainan 70101, Taiwan
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Department of Cell Biology and Anatomy, College of Medicine, National Cheng Kung University, Tainan 70101, Taiwan
*
Author to whom correspondence should be addressed.
Materials 2019, 12(20), 3308; https://doi.org/10.3390/ma12203308
Received: 7 September 2019 / Revised: 30 September 2019 / Accepted: 5 October 2019 / Published: 11 October 2019
(This article belongs to the Section Biomaterials)
Three-dimensional (3D) cell culture models have become powerful tools because they better simulate the in vivo pathophysiological microenvironment than traditional two-dimensional (2D) monolayer cultures. Tumor cells cultured in a 3D system as multicellular cancer aggregates (MCAs) recapitulate several critical in vivo characteristics that enable the study of biological functions and drug discovery. The microwell, in particular, has emerged as a revolutionary technology in the generation of MCAs as it provides geometrically defined microstructures for culturing size-controlled MCAs amenable for various downstream functional assays. This paper presents a simple and economical microwell fabrication methodology that can be conveniently incorporated into a conventional laboratory setting and used for the discovery of therapeutic interventions for liver cancer. The microwells were 400–700 µm in diameter, and hepatic MCAs (Huh-7 cells) were cultured in them for up to 5 days, over which time they grew to 250–520 µm with good viability and shape. The integrability of the microwell fabrication with a high-throughput workflow was demonstrated using a standard 96-well plate for proof-of-concept drug screening. The IC50 of doxorubicin was determined to be 9.3 µM under 2D conditions and 42.8 µM under 3D conditions. The application of photothermal treatment was demonstrated by optimizing concanavalin A-FITC conjugated silica-carbon hollow spheres (SCHSs) at a concentration of 500:200 µg/mL after a 2 h incubation to best bind with MCAs. Based on this concentration, which was appropriate for further photothermal treatment, the relative cell viability was assessed through exposure to a 3 W/cm2 near-infrared laser for 20 min. The relative fluorescence intensity showed an eight-fold reduction in cell viability, confirming the feasibility of using photothermal treatment as a potential therapeutic intervention. The proposed microwell integration is envisioned to serve as a simple in-house technique for the generation of MCAs useful for discovering therapeutic modalities for liver cancer treatment. View Full-Text
Keywords: multicellular cancer aggregates; multicellular tumor spheroids; microwell; liver cancer; doxorubicin; photothermal treatment multicellular cancer aggregates; multicellular tumor spheroids; microwell; liver cancer; doxorubicin; photothermal treatment
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Chiu, C.-Y.; Chen, Y.-C.; Wu, K.-W.; Hsu, W.-C.; Lin, H.-P.; Chang, H.-C.; Lee, Y.-C.; Wang, Y.-K.; Tu, T.-Y. Simple In-House Fabrication of Microwells for Generating Uniform Hepatic Multicellular Cancer Aggregates and Discovering Novel Therapeutics. Materials 2019, 12, 3308.

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