University of Toronto, Department of Chemical Engineering and Applied Chemistry, 200 College St., Toronto, ON, M5S 3E5, Canada.
University of Toronto, Institute of Biomaterials and Biomedical Engineering, 200 College St., Toronto, ON, M5S 3E5, Canada.
Biomaterials. 2018 May;164:54-69. doi: 10.1016/j.biomaterials.2018.01.038. Epub 2018 Feb 19.
Cancer-associated fibroblasts (CAFs) are a key component of the tumour microenvironment and have been shown to play an important role in the progression of cancer. To probe these tumour-stroma interactions, we incorporated CAFs derived from head and neck cancer patients and squamous carcinoma cells of the hypopharynx (FaDu) into the Tissue Roll for the Analysis of Cellular Environment and Response (TRACER) platform to establish a co-culture platform that simulates the CAF-tumour microenvironmental interactions in head and neck tumours. TRACER culture involves infiltrating cells into a thin fibrous scaffold and then rolling the resulting biocomposite around a mandrel to generate a 3D and layered structure. Patterning the fibrous scaffold biocomposite during fabrication enables control over the specific location of different cell populations in the rolled configuration. Here, we optimized the seeding densities and configurations of the CAF and FaDu cell tissue sections to enable a robust 3D co-culture system under normoxic conditions. Co-culture of CAFs with FaDu cells produced negligible effects on radiation resistance, but did produce increases in proliferation rate and invasive cell migration at 24 and 48 h of culture. Our study provides the basis for use of our in vitro co-culture TRACER model to investigate the tumour-stroma interactions, and to bridge the translational gap between preclinical and clinical studies.
癌症相关成纤维细胞(CAFs)是肿瘤微环境的一个关键组成部分,已被证明在癌症的进展中发挥着重要作用。为了探究这些肿瘤-基质相互作用,我们将源自头颈部癌症患者的 CAFs 和下咽鳞癌细胞(FaDu)纳入细胞环境和反应分析组织滚轴(TRACER)平台,建立了一个共培养平台,模拟头颈部肿瘤中的 CAF-肿瘤微环境相互作用。TRACER 培养涉及将细胞渗透到薄纤维支架中,然后将所得的生物复合材料卷绕在芯轴上,以生成 3D 分层结构。在制造过程中对纤维支架生物复合材料进行图案化处理,可以控制滚卷结构中不同细胞群体的特定位置。在这里,我们优化了 CAF 和 FaDu 细胞组织切片的接种密度和配置,以在常氧条件下实现稳健的 3D 共培养系统。CAFs 与 FaDu 细胞的共培养对辐射抗性几乎没有影响,但在培养 24 和 48 小时后,确实会增加增殖率和侵袭性细胞迁移。我们的研究为使用我们的体外共培养 TRACER 模型来研究肿瘤-基质相互作用以及弥合临床前和临床研究之间的转化差距提供了基础。