Characterization of multicellular breast tumor spheroids using image data-driven biophysical mathematical modeling

被引:15
|
作者
Bowers, Haley J. [1 ,2 ]
Fannin, Emily E. [1 ]
Thomas, Alexandra [3 ,4 ]
Weis, Jared A. [1 ,2 ,3 ]
机构
[1] Wake Forest Sch Med, Dept Biomed Engn, 575 N Patterson Ave,Suite 530, Winston Salem, NC 27101 USA
[2] Wake Forest Univ, Virginia Tech, Sch Biomed Engn & Sci, Blacksburg, VA 24061 USA
[3] Wake Forest Baptist Med Ctr, Comprehens Canc Ctr, Winston Salem, NC 27157 USA
[4] Wake Forest Baptist Med Ctr, Dept Internal Med, Sect Hematol & Oncol, Winston Salem, NC USA
基金
美国国家卫生研究院;
关键词
3-DIMENSIONAL CELL-CULTURE; IN-VITRO; CANCER; DRUG; CRITERIA; MATRIX;
D O I
10.1038/s41598-020-68324-4
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
Multicellular tumor spheroid (MCTS) systems provide an in vitro cell culture model system which mimics many of the complexities of an in vivo solid tumor and tumor microenvironment, and are often used to study cancer cell growth and drug efficacy. Here, we present a coupled experimental-computational framework to estimate phenotypic growth and biophysical tumor microenvironment properties. This novel framework utilizes standard microscopy imaging of MCTS systems to drive a biophysical mathematical model of MCTS growth and mechanical interactions. By extending our previous in vivo mechanically-coupled reaction-diffusion modeling framework we developed a microscopy image processing framework capable of mechanistic characterization of MCTS systems. Using MDA-MB-231 breast cancer MCTS, we estimated biophysical parameters of cellular diffusion, rate of cellular proliferation, and cellular tractions forces. We found significant differences in these model-based biophysical parameters throughout the treatment time course between untreated and treated MCTS systems, whereas traditional size-based morphometric parameters were inconclusive. The proposed experimental-computational framework estimates mechanistic MCTS growth and invasion parameters with significant potential to assist in better and more precise assessment of in vitro drug efficacy through the development of computational analysis methodologies for three-dimensional cell culture systems to improve the development and evaluation of antineoplastic drugs.
引用
收藏
页数:12
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