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2D and 3D in vitro culture methods to investigate endothelial-cell enhanced tumor angiogenesis

机译:2D和3D体外培养方法研究内皮细胞增强的肿瘤血管生成

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The reciprocal interactions between endothelial cells and tumor cells to regulate angiogenesis is an important area of cancer research. However, understanding the influential role of endothelial cells on tumorigenesis is highly dependent on the culture systems utilized to study this dynamic and complex process. In contrast to 2D culture systems or the complex host environment of in vivo models, 3D in vitro cancer models have the potential to provide important insights into cellular differentiation, migration, and gene expression in a controlled and well-defined manner. Our preliminary results demonstrating increased cancer cell expression of pro-angiogenic growth factors (VEGF and ANG2) in response to 2D co-culture with endothelial cells motivated the development of a 3D co-culture system to further investigate this phenomena. Assessment of important morphological changes such as cell proliferation, migration, and vessel permeability in response to increased angiogenic activity will be better accommodated in a more physiologically relevant culture environment, therefore permitting the development of more accurate experimental conclusions.
机译:内皮细胞与肿瘤细胞之间的相互作用以调节血管生成是癌症研究的重要领域。然而,了解内皮细胞对肿瘤发生的影响作用高度依赖于用于研究这一动态而复杂的过程的培养系统。与2D培养系统或体内模型的复杂宿主环境相比,3D体外癌症模型具有以可控且定义明确的方式为细胞分化,迁移和基因表达提供重要见解的潜力。我们的初步结果表明,与血管内皮细胞进行2D共培养后,促血管生成生长因子(VEGF和ANG2)的癌细胞表达增加,这推动了3D共培养系统的发展,以进一步研究这一现象。响应于增加的血管生成活性,重要的形态学变化(如细胞增殖,迁移和血管通透性)的评估将更好地适应于生理相关性更高的培养环境,因此可以开发出更准确的实验结论。

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