Center for Molecular Imaging, Department of Radiology, University of Michigan Medical School, 109 Zina Pitcher Place, Ann Arbor, MI 48109-2200, United States.
Center for Molecular Imaging, Department of Radiology, University of Michigan Medical School, 109 Zina Pitcher Place, Ann Arbor, MI 48109-2200, United States; Department of Biomedical Engineering, University of Michigan Medical School, United States; Department of Microbiology and Immunology, University of Michigan Medical School, United States.
Acta Biomater. 2018 Jul 15;75:213-225. doi: 10.1016/j.actbio.2018.06.003. Epub 2018 Jun 5.
Extracellular matrix regulates hallmark features of cancer through biochemical and mechanical signals, although mechanistic understanding of these processes remains limited by lack of models that recreate physiology of tumors. To tissue-engineer models that recapitulate three-dimensional architecture and signaling in tumors, there is a pressing need for new materials permitting flexible control of mechanical and biophysical features. We developed a hybrid hydrogel system composed of collagen and alginate to model tumor environments in breast cancer and other malignancies. Material properties of the hydrogel, including stiffness, microstructure and porosimetry, encompass parameters present in normal organs and tumors. The hydrogel possesses a well-organized, homogenous microstructure with adjustable mechanical stiffness and excellent permeability. Upon embedding multicellular tumor spheroids, we constructed a 3D tumor invasion model showing follow-the-leader migration with fibroblasts leading invasion of cancer cells similar to in vivo. We also demonstrated effects of CXCL12-CXCR4 signaling, a pathway implicated in tumor progression and metastasis, in a dual-tumor spheroid invasion model in 3D hydrogels. These studies establish a new hydrogel platform with material properties that can be tuned to investigate effects of environmental conditions on tumor progression, which will advance future studies of cancer cell invasion and response to therapy.
Our manuscript describes a novel design of hybrid hydrogel system composed of collagen and alginate modeling 3D tumor environments in breast cancer. The hydrogel possesses a well-organized, homogenous microstructure with adjustable mechanical stiffness. Upon embedding tumor spheroids, we successfully showed a 3D tumor invasion model showing follow-the-leader migration with fibroblasts leading invasion of cancer cells similar to in vivo. To the best of our knowledge, this is the first study showing two spheroids invade simultaneously and forming bridge-like connection and effects of chemical gradients in 3D hydrogel environment. This research provides a new model for tumor-stromal interactions in cancer cell migration and establishes a novel hydrogel system for analyzing physical and biochemical signals regulating cancer progression and response to therapy.
细胞外基质通过生化和机械信号调节癌症的标志性特征,尽管这些过程的机制理解仍然受到缺乏能够重现肿瘤生理学的模型的限制。为了组织工程化能够重现肿瘤三维结构和信号的模型,迫切需要新的材料来灵活控制机械和生物物理特性。我们开发了一种由胶原蛋白和藻酸盐组成的混合水凝胶系统,用于模拟乳腺癌和其他恶性肿瘤的肿瘤环境。水凝胶的材料特性,包括硬度、微观结构和孔隙率,包含了正常器官和肿瘤中存在的参数。该水凝胶具有组织有序、均匀的微观结构,可调节机械硬度和优异的渗透性。在嵌入多细胞肿瘤球体后,我们构建了一个 3D 肿瘤侵袭模型,显示了成纤维细胞引导癌细胞类似体内的“跟跑”迁移的侵袭。我们还在 3D 水凝胶中的双肿瘤球体侵袭模型中证明了 CXCL12-CXCR4 信号通路的作用,该通路与肿瘤进展和转移有关。这些研究建立了一个具有可调节材料特性的新型水凝胶平台,可以用来研究环境条件对肿瘤进展的影响,这将推进癌症细胞侵袭和对治疗反应的未来研究。
我们的论文描述了一种由胶原蛋白和藻酸盐组成的新型混合水凝胶系统的设计,用于模拟乳腺癌中的 3D 肿瘤环境。该水凝胶具有组织有序、均匀的微观结构,可调节机械硬度。在嵌入肿瘤球体后,我们成功地展示了一个 3D 肿瘤侵袭模型,显示了成纤维细胞引导癌细胞类似体内的“跟跑”迁移的侵袭。据我们所知,这是第一个显示两个球体同时侵袭并形成桥接连接以及在 3D 水凝胶环境中化学梯度影响的研究。这项研究为癌症细胞迁移中的肿瘤-基质相互作用提供了一个新模型,并为分析调节癌症进展和对治疗反应的物理和生化信号建立了一种新型水凝胶系统。