Evaluation of anticancer drug in a polymer 3D cell chip

被引:6
作者
Lee, Kwon-Jai [1 ]
An, Jeung Hee [2 ]
Shin, Jae-Soo [1 ]
Ha, Cheol Woo [3 ]
Son, Yong [3 ]
Seok, Jaeseo [4 ]
Lee, Kwang-Sup [4 ]
机构
[1] Daejeon Univ, Dept Adv Mat Engn, Daejeon 34520, South Korea
[2] Konkuk Univ, Div Food Biosci, Chungju 27478, South Korea
[3] Korea Adv Inst Sci & Technol, Sch Mech Engn & Aerosp Syst, Daejeon 305701, South Korea
[4] Hannam Univ, Dept Adv Mat & Chem Engn, Daejeon 305811, South Korea
基金
新加坡国家研究基金会;
关键词
CULTURE; CANCER; MECHANISMS; RESISTANCE; SPHEROIDS; PLATFORM;
D O I
10.1364/OME.7.002752
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Three-dimensional (3D) models play an important role in understanding the behavior of a tumor in a well-defined microenvironment, because some aspects of tumor characteristics cannot be fully recapitulated in cell monolayers. In this study, a novel method is presented for the culture of tumor spheroids and for in vivo 3D cell growth simulation of a tumor on a 3D cell chip fabricated in the 3rd floor structure. Scanning electron microscopy and confocal imaging show that, soon after the adjacent tumor adheres to the micropatterned pillar sidewalls, they are subsequently pulled between the pillars in a suspended position. The half maximal inhibitory concentration (IC50) values of mitroxanthrone in the two-dimensional (2D) plate were at the concentration of 345.65 mu g/ml. In contrast, the IC50 value of 3D mitroxanthrone in the 3D cell chip was not detected at the system. Our results indicated that 3D spheroids are generated in uniformly fabricated cancer cell chips, and large numbers of morphologically homogenous spheroids are easily produced. The result showed that the 3D cancer cell chip is more resistant to anticancer agents than 2D plate cell culture. Thus, the 3D cancer cell chip could be used for high-throughput investigations of the efficacy vs. toxicity of drugs or numerous other cancer spheroid cellular and biochemical assays. (C) 2017 Optical Society of America
引用
收藏
页码:2752 / 2759
页数:8
相关论文
共 28 条
[1]   Skin Fibroblast Cells on 3D Skin Cell Chip Using Nanogold Platform Structures and Three-Floor Structures [J].
An, Jeung Hee ;
Lee, Kwon-Jai ;
Kim, Dong-Hee ;
Chae, Ha Neul ;
Lee, Kwang-Sup .
Science of Advanced Materials, 2016, 8 (11) :2147-2152
[2]  
[Anonymous], 2016, NANOTECHNOLOGY, DOI DOI 10.1088/0957-4484/27/1/015701
[3]   Three-dimensional cell culture: the missing link in drug discovery [J].
Breslin, Susan ;
O'Driscoll, Lorraine .
DRUG DISCOVERY TODAY, 2013, 18 (5-6) :240-249
[4]   A tense situation: forcing tumour progression [J].
Butcher, Darci T. ;
Alliston, Tamara ;
Weaver, Valerie M. .
NATURE REVIEWS CANCER, 2009, 9 (02) :108-122
[5]   Differences in growth properties of endometrial cancer in three dimensional (3D) culture and 2D cell monolayer [J].
Chitcholtan, Kenny ;
Asselin, Eric ;
Parent, Sophie ;
Sykes, Peter H. ;
Evans, John J. .
EXPERIMENTAL CELL RESEARCH, 2013, 319 (01) :75-87
[6]   Modelling glandular epithelial cancers in three-dimensional cultures [J].
Debnath, J ;
Brugge, JS .
NATURE REVIEWS CANCER, 2005, 5 (09) :675-688
[7]   Cells on chips [J].
El-Ali, Jamil ;
Sorger, Peter K. ;
Jensen, Klavs F. .
NATURE, 2006, 442 (7101) :403-411
[8]   Mechanisms of cancer drug resistance [J].
Gottesman, MM .
ANNUAL REVIEW OF MEDICINE, 2002, 53 :615-627
[9]   From 3D cell culture to organs-on-chips [J].
Huh, Dongeun ;
Hamilton, Geraldine A. ;
Ingber, Donald E. .
TRENDS IN CELL BIOLOGY, 2011, 21 (12) :745-754
[10]   Microscale culture of human liver cells for drug development [J].
Khetani, Salman R. ;
Bhatia, Sangeeta N. .
NATURE BIOTECHNOLOGY, 2008, 26 (01) :120-126