Label-free drug response evaluation of human derived tumor spheroids using three-dimensional dynamic optical coherence tomography

被引:15
作者
Abd El-Sadek, Ibrahim [1 ,2 ]
Shen, Larina Tzu-Wei [3 ]
Mori, Tomoko [3 ]
Makita, Shuichi [1 ]
Mukherjee, Pradipta [1 ]
Lichtenegger, Antonia [1 ,4 ]
Matsusaka, Satoshi [3 ]
Yasuno, Yoshiaki [1 ]
机构
[1] Univ Tsukuba, Computat Opt Grp, Tsukuba, Ibaraki 3058573, Japan
[2] Damietta Univ, Dept Phys, Fac Sci, New Damietta 34517, Damietta, Egypt
[3] Univ Tsukuba, Clin Res & Reg Innovat, Fac Med, Tsukuba, Ibaraki 3058575, Japan
[4] Med Univ Vienna, Ctr Med Phys & Biomed Engn, A-1090 Vienna, Austria
基金
日本科学技术振兴机构; 奥地利科学基金会; 日本学术振兴会;
关键词
CANCER CELL-LINES; APOPTOSIS; CONTRAST; DOXORUBICIN; MECHANISM; MOTILITY; TISSUES; ARREST; MOTION; SN-38;
D O I
10.1038/s41598-023-41846-3
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
This study aims at demonstrating label -free drug -response -patterns assessment of different tumor spheroids and drug types by dynamic optical coherence tomography (D-OCT). The study involved human breast cancer (MCF-7) and colon cancer (HT -29) spheroids. The MCF-7 and HT -29 spheroids were treated with paclitaxel (Taxol; PTX) and the active metabolite of irinotecan SN-38, respectively. The drugs were applied with 0 (control), 0.1, 1, and 10 mu M concentrations and the treatment durations were 1, 3, and 6 days. A swept -source OCT microscope equipped with a repeated raster scanning protocol was used to scan the spheroids. Logarithmic intensity variance (LIV) and late OCT correlation decay speed (OCDSl) algorithms were used to visualize the tumor spheroid dynamics. LIV and OCDSl images visualized different response patterns of the two types of spheroids. In addition, spheroid morphology, LIV, and OCDSl quantification showed different time -courses among the spheroid and drug types. These results may indicate different action mechanisms of the drugs. The results showed the feasibility of D-OCT for the evaluation of drug response patterns of different cell spheroids and drug types and suggest that D-OCT can perform anti -cancer drug testing.
引用
收藏
页数:15
相关论文
共 73 条
[21]   Multicellular tumor spheroids: An underestimated tool is catching up again [J].
Hirschhaeuser, Franziska ;
Menne, Heike ;
Dittfeld, Claudia ;
West, Jonathan ;
Mueller-Klieser, Wolfgang ;
Kunz-Schughart, Leoni A. .
JOURNAL OF BIOTECHNOLOGY, 2010, 148 (01) :3-15
[22]   The CytoskeletonA Complex Interacting Meshwork [J].
Hohmann, Tim ;
Dehghani, Faramarz .
CELLS, 2019, 8 (04)
[23]  
HSIANG YH, 1989, CANCER RES, V49, P5077
[24]   Optical Coherence Tomography Detects Necrotic Regions and Volumetrically Quantifies Multicellular Tumor Spheroids [J].
Huang, Yongyang ;
Wang, Shunqiang ;
Guo, Qiongyu ;
Kessel, Sarah ;
Rubinoff, Ian ;
Chan, Leo Li-Ying ;
Li, Peter ;
Liu, Yaling ;
Qiu, Jean ;
Zhou, Chao .
CANCER RESEARCH, 2017, 77 (21) :6011-6020
[25]   Rapid generation of single-tumor spheroids for high-throughput cell function and toxicity analysis [J].
Ivascu, Andrea ;
Kubbies, Manfred .
JOURNAL OF BIOMOLECULAR SCREENING, 2006, 11 (08) :922-932
[26]   Short-term spheroid culture of primary colorectal cancer cells as an in vitro model for personalizing cancer medicine [J].
Jeppesen, Maria ;
Hagel, Grith ;
Glenthoj, Anders ;
Vainer, Ben ;
Ibsen, Per ;
Harling, Henrik ;
Thastrup, Ole ;
Jorgensen, Lars N. ;
Thastrup, Jacob .
PLOS ONE, 2017, 12 (09)
[28]   Actin cytoskeleton controls movement of intracellular organelles in pancreatic duct epithelial cells [J].
Jung, Seung-Ryoung ;
Seo, Jong Bae ;
Shim, Donghwan ;
Hille, Bertil ;
Koh, Duk-Su .
CELL CALCIUM, 2012, 51 (06) :459-469
[29]  
KAWATO Y, 1991, CANCER RES, V51, P4187
[30]   Intracellular motility: How can we all work together? [J].
Kelleher, JF ;
Titus, MA .
CURRENT BIOLOGY, 1998, 8 (11) :R394-R397