Department of Aerospace and Mechanical Engineering, University of Notre Dame, Notre Dame, IN 46556, United States.
Bioengineering Graduate Program, University of Notre Dame, Notre Dame, IN 46556, United States.
Acta Biomater. 2020 Apr 1;106:1-21. doi: 10.1016/j.actbio.2020.02.006. Epub 2020 Feb 9.
The mechanisms behind cancer initiation and progression are not clear. Therefore, development of clinically relevant models to study cancer biology and drug response in tumors is essential. In vivo models are very valuable tools for studying cancer biology and for testing drugs; however, they often suffer from not accurately representing the clinical scenario because they lack either human cells or a functional immune system. On the other hand, two-dimensional (2D) in vitro models lack the three-dimensional (3D) network of cells and extracellular matrix (ECM) and thus do not represent the tumor microenvironment (TME). As an alternative approach, 3D models have started to gain more attention, as such models offer a platform with the ability to study cell-cell and cell-material interactions parametrically, and possibly include all the components present in the TME. Here, we first give an overview of the breast cancer TME, and then discuss the current state of the pre-clinical breast cancer models, with a focus on the engineered 3D tissue models. We also highlight two engineering approaches that we think are promising in constructing models representative of human tumors: 3D printing and microfluidics. In addition to giving basic information about the TME in the breast tissue, this review article presents the state-of-the-art tissue engineered breast cancer models. STATEMENT OF SIGNIFICANCE: Involvement of biomaterials and tissue engineering fields in cancer research enables realistic mimicry of the cell-cell and cell-extracellular matrix (ECM) interactions in the tumor microenvironment (TME), and thus creation of better models that reflect the tumor response against drugs. Engineering the 3D in vitro models also requires a good understanding of the TME. Here, an overview of the breast cancer TME is given, and the current state of the pre-clinical breast cancer models, with a focus on the engineered 3D tissue models is discussed. This review article is useful not only for biomaterials scientists aiming to engineer 3D in vitro TME models, but also for cancer researchers willing to use these models for studying cancer biology and drug testing.
癌症发生和发展的机制尚不清楚。因此,开发临床相关的模型来研究肿瘤中的癌症生物学和药物反应是至关重要的。体内模型是研究癌症生物学和测试药物的非常有价值的工具;然而,由于缺乏人类细胞或功能性免疫系统,它们往往不能准确地代表临床情况。另一方面,二维(2D)体外模型缺乏细胞和细胞外基质(ECM)的三维(3D)网络,因此不能代表肿瘤微环境(TME)。作为一种替代方法,3D 模型开始受到更多关注,因为这种模型提供了一个能够参数化研究细胞-细胞和细胞-材料相互作用的平台,并且可能包含 TME 中存在的所有成分。在这里,我们首先概述了乳腺癌 TME,然后讨论了目前临床前乳腺癌模型的状态,重点介绍了工程 3D 组织模型。我们还强调了两种我们认为在构建代表人类肿瘤的模型方面很有前途的工程方法:3D 打印和微流控。除了提供乳腺组织中 TME 的基本信息外,本文还介绍了最先进的组织工程乳腺癌模型。
生物材料和组织工程领域在癌症研究中的参与使得能够真实模拟肿瘤微环境(TME)中的细胞-细胞和细胞-细胞外基质(ECM)相互作用,从而创建更好地反映肿瘤对药物反应的模型。工程 3D 体外模型还需要很好地了解 TME。在这里,我们概述了乳腺癌 TME,并讨论了目前临床前乳腺癌模型的状态,重点介绍了工程 3D 组织模型。本文不仅对旨在工程 3D 体外 TME 模型的生物材料科学家有用,而且对愿意使用这些模型研究癌症生物学和药物测试的癌症研究人员也有用。