Tumor Growth Analysis of Ewing Sarcoma Cell Lines Using Subcutaneous Xenografts in Mice
- PMID: 33326103
- DOI: 10.1007/978-1-0716-1020-6_15
Tumor Growth Analysis of Ewing Sarcoma Cell Lines Using Subcutaneous Xenografts in Mice
Abstract
Subcutaneous murine xenograft models are one of the most commonly used in vivo experimental methods in the cancer research field. Due to the lack of appropriate animal models for Ewing sarcoma, subcutaneous murine xenograft models currently offer the simplest way to investigate antineoplastic effects of therapeutics or biological functions of target genes in vivo. In order to properly carry out tumor growth analysis via subcutaneous xenografts of Ewing sarcoma cells many factors should be taken into account beforehand at the planning phase of experiments. Therefore, in this chapter we describe in detail a widely used procedure for subcutaneous injection in mice, focusing on the specific characteristics of Ewing sarcoma cell lines.
Keywords: Ewing sarcoma; Immunocompromised mice; Subcutaneous injection; Xenografts.
References
-
- Kerbel RS (2003) Human tumor xenografts as predictive preclinical models for anticancer drug activity in humans: better than commonly perceived-but they can be improved. Cancer Biol Ther 2:S134–S139 - PubMed
-
- Kelland LR (2004) Of mice and men: values and liabilities of the athymic nude mouse model in anticancer drug development. Eur J Cancer 40:827–836 - DOI
-
- Ding Y, Cravero JD, Adrian K et al (2010) Modeling pancreatic cancer in vivo: from xenograft and carcinogen-induced systems to genetically engineered mice. Pancreas 39:283–292 - DOI
-
- Nielsen SW (1976) Comparative pathology of bone tumors in animals, with particular emphasis on the dog. In: Grundmann E (ed) Malignant bone tumors. Recent results in cancer research/Fortschritte der Krebsforschung/Progrès dans les recherches Sur le cancer, vol 54. Springer, Berlin, Heidelberg, pp 3–16
-
- Sharkey FE, Fogh J (1979) Incidence and pathological features of spontaneous tumors in athymic nude mice. Cancer Res 39:833–839 - PubMed
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Medical
