4.4 Article

The In ovo CAM-assay as a Xenograft Model for Sarcoma

Journal

JOVE-JOURNAL OF VISUALIZED EXPERIMENTS
Volume -, Issue 77, Pages -

Publisher

JOURNAL OF VISUALIZED EXPERIMENTS
DOI: 10.3791/50522

Keywords

Cancer Biology; Issue 77; Medicine; Cellular Biology; Molecular Biology; Biomedical Engineering; Bioengineering; Developmental Biology; Anatomy; Physiology; Oncology; Surgery; Adipose Tissue; Connective Tissue; Neoplasm; Muscle Tissue; Sarcoma; Animal Experimentation; Cell Culture Techniques; Neoplasms; Experimental; Neoplasm Transplantation; Biological Assay; Sarcomas; CAM-assay; CAM; assay; xenograft; proliferation; invasion; cancer; tumor; in ovo; animal model

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Sarcoma is a very rare disease that is heterogeneous in nature, all hampering the development of new therapies. Sarcoma patients are ideal candidates for personalized medicine after stratification, explaining the current interest in developing a reproducible and low-cost xenotransplant model for this disease. The chick chorioallantoic membrane is a natural immunodeficient host capable of sustaining grafted tissues and cells without species-specific restrictions. In addition, it is easily accessed, manipulated and imaged using optical and fluorescence stereomicroscopy. Histology further allows detailed analysis of heterotypic cellular interactions. This protocol describes in detail the in ovo grafting of the chorioallantoic membrane with fresh sarcoma-derived tumor tissues, their single cell suspensions, and permanent and transient fluorescently labeled established sarcoma cell lines (Saos-2 and SW1353). The chick survival rates are up to 75%. The model is used to study graft-(viability, Ki67 proliferation index, necrosis, infiltration) and host (fibroblast infiltration, vascular ingrowth) behavior. For localized grafting of single cell suspensions, ECM gel provides significant advantages over inert containment materials. The Ki67 proliferation index is related to the distance of the cells from the surface of the CAM and the duration of application on the CAM, the latter determining a time frame for the addition of therapeutic products.

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