A Microdevice Platform Recapitulating Hypoxic Tumor Microenvironments

被引:31
作者
Ando, Yuta [1 ]
Ta, Hoang P. [1 ]
Yen, Daniel P. [1 ]
Lee, Sang-Sin [1 ]
Raola, Sneha [1 ]
Shen, Keyue [1 ,2 ,3 ]
机构
[1] Univ Southern Calif, Viterbi Sch Engn, Dept Biomed Engn, Los Angeles, CA 90089 USA
[2] Univ Southern Calif, Keck Sch Med, Norris Comprehens Canc Ctr, Los Angeles, CA 90033 USA
[3] Univ Southern Calif, Keck Sch Med, Dept Stem Cell Biol & Regenerat Med, Los Angeles, CA 90033 USA
来源
SCIENTIFIC REPORTS | 2017年 / 7卷
关键词
CELL-CULTURE; MESENCHYMAL TRANSITION; EXTRACELLULAR-MATRIX; CANCER PROGRESSION; OXYGEN LEVELS; IN-VIVO; MODELS; TIRAPAZAMINE; INDUCTION; DIFFUSION;
D O I
10.1038/s41598-017-15583-3
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Hypoxia plays a central role in cancer progression and resistance to therapy. We have engineered a microdevice platform to recapitulate the intratumor oxygen gradients that drive the heterogeneous hypoxic landscapes in solid tumors. Our design features a "tumor section"-like culture by incorporating a cell layer between two diffusion barriers, where an oxygen gradient is established by cellular metabolism and physical constraints. We confirmed the oxygen gradient by numerical simulation and imaging-based oxygen sensor measurement. We also demonstrated spatially-resolved hypoxic signaling in cancer cells through immunostaining, gene expression assay, and hypoxia-targeted drug treatment. Our platform can accurately generate and control oxygen gradients, eliminates complex microfluidic handling, allows for incorporation of additional tumor components, and is compatible with high-content imaging and high-throughput applications. It is well suited for understanding hypoxia-mediated mechanisms in cancer disease and other biological processes, and discovery of new therapeutics.
引用
收藏
页数:12
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