One Hour In Vivo-like Phenotypic Screening System for Anti-cancer Drugs Using a High Precision Surface Plasmon Resonance Device

被引:4
|
作者
Johzuka, Junko [1 ,2 ]
Ona, Toshihiro [1 ,2 ]
Nomura, Masatoshi [3 ]
机构
[1] OAtari Inc, 4F Chikusui Bld,1-4-11 Chuo, Fukuoka, Fukuoka 8160942, Japan
[2] Kyushu Univ, Global Innovat Ctr, Grad Sch Bioresource & Bioenvironm Sci, 6-1 Kasuga Kouen, Fukuoka, Fukuoka 8168580, Japan
[3] Kyushu Univ Hosp, Dept Endocrine & Metab Dis Diabet Mellitus, Higashi Ku, 3-1-1 Maidashi, Fukuoka, Fukuoka 8128582, Japan
基金
日本科学技术振兴机构;
关键词
Surface plasmon resonance sensor; label-free biosensing; in vivo-like phenotypic screening; anti-cancer drugs; TEST CD-DST; CELL-CULTURE; PANCREATIC-CANCER; SENSITIVITY TEST; TUMOR SPHEROIDS; VITRO; 3D; CHEMOSENSITIVITY; EXPRESSION; MICROSCOPY;
D O I
10.2116/analsci.18P013
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In anti-cancer drug (candidate) screening, there is the need for evaluation at physiological concentrations similar to in vivo. This is often performed by three-dimensionally (3D) cultured cells; however, it requires a long culture period of 2 - 4 weeks with tedious experimental procedures. Here, we report on a high precision surface plasmon resonance (HP-SPR)-3D system. We developed the system with average fluctuation of 50 ndeg s(-1) using two-dimensionally cultured cells attached onto a sensor chip by applying collagen on the top to change their activity into in vivo-like conditions without cell division. It allowed in vivo-like phenotypic screening for anti-cancer drugs within 1 h of drug addition. The data were collected as the stable linear signal change parts for at least 5 min after 25 min following drug addition. The results provided compatibility to clinically related chemosensitivity test for anti-cancer (P <0.001) using two cell lines of pancreatic cancer and three anti-cancer drugs to represent differences in individual gene expression and drug mode of action.
引用
收藏
页码:1189 / 1194
页数:6
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