Engineered 3D ex vivo models to recapitulate the complex stromal and immune interactions within the tumor microenvironment

被引:12
作者
Ravi, Kalpana [1 ]
Manoharan, Twinkle Jina Minette [1 ]
Wang, Kuei-Chun [1 ]
Pockaj, Barbara [3 ]
Nikkhah, Mehdi [1 ,2 ]
机构
[1] Arizona State Univ, Sch Biol & Hlth Syst Engn SBHSE, Tempe, AZ 85287 USA
[2] Arizona State Univ, Biodesign Virginia G Piper Ctr Personalized Diagno, Tempe, AZ 85287 USA
[3] Mayo Clin, Dept Surg, Phoenix, AZ USA
关键词
3D-engineered models; Microfluidics; Tumor microenvironment (TME); Tumor immune microenvironment (TIME); 3D printed; Immune crosstalk; Tumor-on-chip; IN-VITRO MODEL; BREAST-CANCER CELLS; DENDRITIC CELLS; LUNG-CANCER; CROSS-TALK; T-CELLS; CULTURE; MACROPHAGES; FIBROBLASTS; ORGANOIDS;
D O I
10.1016/j.biomaterials.2023.122428
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Cancer thrives in a complex environment where interactions between cellular and acellular components, sur-rounding the tumor, play a crucial role in disease development and progression. Despite significant progress in cancer research, the mechanism driving tumor growth and therapeutic outcomes remains elusive. Two-dimensional (2D) cell culture assays and in vivo animal models are commonly used in cancer research and therapeutic testing. However, these models suffer from numerous shortcomings including lack of key features of the tumor microenvironment (TME) & cellular composition, cost, and ethical clearance. To that end, there is an increased interest in incorporating and elucidating the influence of TME on cancer progression. Advancements in 3D-engineered ex vivo models, leveraging biomaterials and microengineering technologies, have provided an unprecedented ability to reconstruct native-like bioengineered cancer models to study the heterotypic in-teractions of TME with a spatiotemporal organization. These bioengineered cancer models have shown excellent capabilities to bridge the gap between oversimplified 2D systems and animal models. In this review article, we primarily provide an overview of the immune and stromal cellular components of the TME and then discuss the latest state-of-the-art 3D-engineered ex vivo platforms aiming to recapitulate the complex TME features. The engineered TME model, discussed herein, are categorized into three main sections according to the cellular interactions within TME: (i) Tumor-Stromal interactions, (ii) Tumor-Immune interactions, and (iii) Complex TME interactions. Finally, we will conclude the article with a perspective on how these models can be instrumental for cancer translational studies and therapeutic testing.
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页数:30
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