Chemical Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, United States.
Lab Chip. 2013 May 21;13(10):1969-78. doi: 10.1039/c3lc41300d. Epub 2013 Apr 5.
The cancer microenvironment, which incorporates interactions with stromal cells, extracellular matrix (ECM), and other tumor cells in a 3-dimensional (3D) context, has been implicated in every stage of cancer development, including growth of the primary tumor, metastatic spread, and response to treatment. Our understanding of the tumor microenvironment and our ability to develop new therapies would greatly benefit from tools that allow us to systematically probe microenvironmental cues within a 3D context. Here, we leveraged recent advances in microfluidic technology to develop a platform for high-throughput fabrication of tunable cellular microniches ("microtissues") that allow us to probe tumor cell response to a range of microenvironmental cues, including ECM, soluble factors, and stromal cells, all in 3D. We further combine this tunable microniche platform with rapid, flow-based population level analysis (n > 500), which permits analysis and sorting of microtissue populations both pre- and post-culture by a range of parameters, including proliferation and homotypic or heterotypic cell density. We used this platform to demonstrate differential responses of lung adenocarcinoma cells to a selection of ECM molecules and soluble factors. The cells exhibited enhanced or reduced proliferation when encapsulated in fibronectin- or collagen-1-containing microtissues, respectively, and they showed reduced proliferation in the presence of TGF-β, an effect that we did not observe in monolayer culture. We also measured tumor cell response to a panel of drug targets and found, in contrast to monolayer culture, specific sensitivity of tumor cells to TGFβR2 inhibitors, implying that TGF-β has an anti-proliferative affect that is unique to the 3D context and that this effect is mediated by TGFβR2. These findings highlight the importance of the microenvironmental context in therapeutic development and that the platform we present here allows the high-throughput study of tumor response to drugs as well as basic tumor biology in well-defined microenvironmental niches.
肿瘤微环境包括与间质细胞、细胞外基质(ECM)和其他肿瘤细胞在三维(3D)环境中的相互作用,已被牵连到癌症发展的各个阶段,包括原发性肿瘤的生长、转移扩散以及对治疗的反应。我们对肿瘤微环境的理解以及开发新疗法的能力将极大地受益于能够在 3D 环境中系统地探测微环境线索的工具。在这里,我们利用微流控技术的最新进展,开发了一个用于高通量制造可调节细胞微环境(“微组织”)的平台,使我们能够探测肿瘤细胞对一系列微环境线索的反应,包括 ECM、可溶性因子和基质细胞,所有这些都在 3D 环境中进行。我们进一步将这个可调节的微环境平台与快速的、基于流动的群体水平分析(n>500)相结合,这允许在培养前后通过一系列参数(包括增殖和同型或异型细胞密度)对微组织群体进行分析和分选。我们使用这个平台来证明肺腺癌细胞对一系列 ECM 分子和可溶性因子的不同反应。当细胞被包裹在含有纤维连接蛋白或胶原蛋白-1 的微组织中时,分别表现出增强或减少的增殖,并且当存在 TGF-β时,它们表现出减少的增殖,而在单层培养中我们没有观察到这种情况。我们还测量了肿瘤细胞对一组药物靶点的反应,与单层培养相比,发现肿瘤细胞对 TGFβR2 抑制剂有特异性的敏感性,这意味着 TGF-β对增殖有抗增殖作用,这种作用是 3D 环境所特有的,这种作用是由 TGFβR2 介导的。这些发现强调了微环境背景在治疗开发中的重要性,并且我们在这里提出的平台允许在明确定义的微环境龛中对肿瘤对药物的反应以及基本的肿瘤生物学进行高通量研究。