The Centenary Institute, Newtown, New South Wales 2042, Australia.
School of Biological Sciences, Universiti Sains Malaysia, 11800 Georgetown, Penang, Malaysia.
Healthcare (Basel). 2013 Dec 23;2(1):27-46. doi: 10.3390/healthcare2010027.
The behavior of melanoma cells has traditionally been studied in vitro in two-dimensional cell culture with cells adhering to plastic dishes. However, in order to mimic the three-dimensional architecture of a melanoma, as well as its interactions with the tumor microenvironment, there has been the need for more physiologically relevant models. This has been achieved by designing 3D in vitro models of melanoma, such as melanoma spheroids embedded in extracellular matrix or organotypic skin reconstructs. In vivo melanoma models have typically relied on the growth of tumor xenografts in immunocompromised mice. Several genetically engineered mouse models have now been developed which allow the generation of spontaneous melanoma. Melanoma models have also been established in other species such as zebrafish, which are more conducive to imaging and high throughput studies. We will discuss these models as well as novel techniques that are relevant to the study of the molecular mechanisms underlying melanoma progression.
黑色素瘤细胞的行为传统上是在二维细胞培养中通过使细胞附着在塑料培养皿上进行体外研究的。然而,为了模拟黑色素瘤的三维结构及其与肿瘤微环境的相互作用,需要更具生理相关性的模型。这是通过设计黑色素瘤的 3D 体外模型来实现的,例如嵌入细胞外基质中的黑色素瘤球体或器官型皮肤重建。体内黑色素瘤模型通常依赖于在免疫功能低下的小鼠中生长肿瘤异种移植物。现在已经开发出几种基因工程小鼠模型,可用于生成自发性黑色素瘤。黑色素瘤模型也已在其他物种中建立,例如斑马鱼,斑马鱼更有利于成像和高通量研究。我们将讨论这些模型以及与研究黑色素瘤进展相关的分子机制的新技术。