Li Michael, Pathak Ravi R, Lopez-Rivera Esther, Friedman Scott L, Aguirre-Ghiso Julio A, Sikora Andrew G
Department of Medicine, Division of Liver Diseases, Icahn School of Medicine at Mount Sinai; Department of Otolaryngology, Icahn School of Medicine at Mount Sinai.
Bobby R. Alford Department of Otolaryngology - Head and Neck Surgery, Baylor College of Medicine.
J Vis Exp. 2015 Oct 9(104):52411. doi: 10.3791/52411.
The chick chorioallantoic membrane (CAM) begins to develop by day 7 after fertilization and matures by day 12. The CAM is naturally immunodeficient and highly vascularized, making it an ideal system for tumor implantation. Furthermore, the CAM contains extracellular matrix proteins such as fibronectin, laminin, collagen, integrin alpha(v)beta3, and MMP-2, making it an attractive model to study tumor invasion and metastasis. Scientists have long taken advantage of the physiology of the CAM by using it as a model of angiogenesis. More recently, the CAM assay has been modified to work as an in vivo xenograft model system for various cancers that bridges the gap between basic in vitro work and more complex animal cancer models. The CAM assay allows for the study of tumor growth, anti-tumor therapies, and pro-tumor molecular pathways in a biologically relevant system that is both cost- and time-effective. Here, we describe the development of CAM xenograft model of hepatocellular carcinoma (HCC) with embryonic survival rates of up to 93% and reliable tumor take leading to growth of three-dimensional, vascularized tumors.
鸡胚绒毛尿囊膜(CAM)在受精后第7天开始发育,第12天成熟。CAM天然免疫缺陷且血管高度丰富,使其成为肿瘤植入的理想系统。此外,CAM含有细胞外基质蛋白,如纤连蛋白、层粘连蛋白、胶原蛋白、整合素α(v)β3和基质金属蛋白酶-2,使其成为研究肿瘤侵袭和转移的有吸引力的模型。长期以来,科学家们一直利用CAM的生理学特性,将其作为血管生成模型。最近,CAM检测方法已被改进,用作各种癌症的体内异种移植模型系统,弥合了基础体外研究与更复杂的动物癌症模型之间的差距。CAM检测能够在一个具有生物学相关性、经济且省时的系统中研究肿瘤生长、抗肿瘤治疗和促肿瘤分子途径。在此,我们描述了肝细胞癌(HCC)CAM异种移植模型的建立,其胚胎存活率高达93%,肿瘤接种可靠,可导致三维血管化肿瘤生长。