Department of Genetic Medicine, Weill Cornell Medical College, Howard Hughes Medical Institute, New York, New York 10065, USA.
Tissue Eng Part A. 2010 Jul;16(7):2157-9. doi: 10.1089/ten.TEA.2010.0183.
Angiogenesis is a fundamental prerequisite for tissue growth and thus an attractive target for cancer therapeutics. However, current efforts to halt tumor growth using antiangiogenic agents have been met with limited success. A reason for this may be that studies aimed at understanding tissue and organ formation have to this point utilized two-dimensional cell culture techniques, which fail to faithfully mimic the pathological architecture of disease in an in vivo context. In this issue of Tissue Engineering, the work of Fischbach-Teschl's group manipulate such variables as oxygen concentration, culture three-dimensionality, and cell-extracellular matrix interactions to more closely approximate the biophysical and biochemical microenvironment of tumor angiogenesis. In this article, we discuss how novel tissue engineering platforms provide a framework for the study of tumorigenesis under pathophysiologically relevant in vitro culture conditions.
血管生成是组织生长的基本前提,因此成为癌症治疗的一个有吸引力的靶点。然而,目前使用抗血管生成药物来阻止肿瘤生长的努力收效甚微。造成这种情况的一个原因可能是,旨在理解组织和器官形成的研究迄今为止一直使用二维细胞培养技术,而这些技术无法在体内环境中真实地模拟疾病的病理结构。在本期《组织工程》中,Fischbach-Teschl 小组的工作通过操纵氧浓度、三维培养和细胞-细胞外基质相互作用等变量,更接近肿瘤血管生成的生物物理和生化微环境。在本文中,我们讨论了新型组织工程平台如何为在病理生理相关的体外培养条件下研究肿瘤发生提供了一个框架。