On-chip modeling of tumor evolution: Advances, challenges and opportunities

被引:15
作者
Li, Chengpan [1 ,2 ]
Holman, Joseph Benjamin [1 ]
Shi, Zhengdi [1 ]
Qiu, Bensheng [1 ,2 ]
Ding, Weiping [3 ]
机构
[1] Univ Sci & Technol China, Dept Elect Engn & Informat Sci, Hefei 230027, Anhui, Peoples R China
[2] Univ Sci & Technol China, Ctr Biomed Imaging, Hefei 230027, Anhui, Peoples R China
[3] Univ Sci & Technol China, Affiliated Hosp 1, Dept Oncol, Div Life Sci & Med, Hefei 230001, Anhui, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Tumor evolution; Microfluidic chips; Tumor cell behaviors; Solid tumors; Tumor organoids; EPITHELIAL-MESENCHYMAL TRANSITIONS; CELL-CULTURE SYSTEMS; A-CHIP; EXTRACELLULAR-MATRIX; MICROFLUIDIC DEVICE; INTERSTITIAL FLOW; CANCER-CELLS; MIGRATION; SPHEROIDS; PLATFORM;
D O I
10.1016/j.mtbio.2023.100724
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Tumor evolution is the accumulation of various tumor cell behaviors from tumorigenesis to tumor metastasis and is regulated by the tumor microenvironment (TME). However, the mechanism of solid tumor progression has not been completely elucidated, and thus, the development of tumor therapy is still limited. Recently, Tumor chips constructed by culturing tumor cells and stromal cells on microfluidic chips have demonstrated great potential in modeling solid tumors and visualizing tumor cell behaviors to exploit tumor progression. Herein, we review the methods of developing engineered solid tumors on microfluidic chips in terms of tumor types, cell resources and patterns, the extracellular matrix and the components of the TME, and summarize the recent advances of microfluidic chips in demonstrating tumor cell behaviors, including proliferation, epithelial-to-mesenchymal transition, migration, intravasation, extravasation and immune escape of tumor cells. We also outline the combination of tumor organoids and microfluidic chips to elaborate tumor organoid-on-a-chip platforms, as well as the practical limitations that must be overcome.
引用
收藏
页数:20
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