Engineering Biomaterials to Model Immune-Tumor Interactions In Vitro

被引:3
作者
Skirzynska, Arianna [1 ,2 ]
Xue, Chang [2 ,3 ]
Shoichet, Molly S. [1 ,2 ,3 ,4 ]
机构
[1] Univ Toronto, Chem Engn & Appl Chem, 200 Coll St, Toronto, ON M5S 3E5, Canada
[2] Univ Toronto, Terrence Donnelly Ctr Cellular & Biomol Res, 160 Coll St, Toronto, ON M5S 3E1, Canada
[3] Univ Toronto, Inst Biomed Engn, 164 Coll St, Toronto, ON M5S 3G9, Canada
[4] Univ Toronto, Dept Chem, 80 Coll St, Toronto, ON M5S 3H4, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
biomaterials; hydrogels; immune response; tumor evasion; tumor microenvironment; MACROPHAGE PHENOTYPE; METABOLIC PATHWAYS; ALIGNED COLLAGEN; CELL-ACTIVATION; HYALURONIC-ACID; HYDROGEL; POLARIZATION; SCAFFOLDS; MICROENVIRONMENT; MIGRATION;
D O I
10.1002/adma.202310637
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Engineered biomaterial scaffolds are becoming more prominent in research laboratories to study drug efficacy for oncological applications in vitro, but do they have a place in pharmaceutical drug screening pipelines? The low efficacy of cancer drugs in phase II/III clinical trials suggests that there are critical mechanisms not properly accounted for in the pre-clinical evaluation of drug candidates. Immune cells associated with the tumor may account for some of these failures given recent successes with cancer immunotherapies; however, there are few representative platforms to study immune cells in the context of cancer as traditional 2D culture is typically monocultures and humanized animal models have a weakened immune composition. Biomaterials that replicate tumor microenvironmental cues may provide a more relevant model with greater in vitro complexity. In this review, the authors explore the pertinent microenvironmental cues that drive tumor progression in the context of the immune system, discuss how these cues can be incorporated into hydrogel design to culture immune cells, and describe progress toward precision oncological drug screening with engineered tissues. In this review, the authors explore the pertinent microenvironmental cues that drive tumor progression in the context of the immune system, discuss how these cues can be incorporated into hydrogel design to culture immune cells, and describe progress toward precision oncological drug screening with engineered tissues. image
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页数:15
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