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. Author manuscript; available in PMC: 2018 Nov 12.
Published in final edited form as: J Nucl Med. 2016 Feb;57(Suppl 1):60S–68S. doi: 10.2967/jnumed.115.157917

Table 2.

Preclinical Murine Models of Human Cancer

Model Main components Advantages Limitations Time and Cost*
Xenograft (cell line) Immortalized human tumor cell lines transplanted into immunodeficient host (mouse) Numerous established and well-annotated cell lines Immunodeficient host 2–4 wk, $
Representation from various human tumor types Subcutaneous location may not allow cultivation of key tissue-specific stromal infiltrate
Features of tumor microenvironment, including stromal and vascular cells, incorporated within tumor Cross-species divide; stromal components are mouse, whereas tumor cells are human
Tumors are easily and precisely measured Limited or no genetic heterogeneity present within tumor
Xenograft (patient-derived) Human tumor explant propagated in immunodeficient host (mouse) Heterogeneity and genetic diversity within tumors Immunodeficient host 8–24 wk, $$$
Representation from various human tumor types Subcutaneous location may not allow cultivation of key tissue-specific stromal infiltrate
Features of tumor microenvironment, including stromal and vascular cells, incorporated within tumor Surgical implantation required
Tumors are easily and precisely measured Cross-species divide; stromal components are mouse, whereas tumor cells are human
Genetic and phenotypic drift with passage
Syngeneic Immortalized mouse tumor cell line allografted into immunocompetent host (mouse) Presence of intact immune system Limited number of established cell lines, which are poorly annotated 2–4 wk, $
Features of tumor microenvironment, including stromal and vascular cells, incorporated within tumor Strong immunogenicity of some lines promotes spontaneous regression
All cell types within tumor are of mouse origin Rapid growth rate of many lines limits use in longer-term studies
Tumors are easily and precisely measured
GEMMs Genetic modification that permits induced or spontaneous tumor development Tumors develop in tissue of origin Limited genetic mosaicism and heterogeneity of tumors 12–24 wk†, $$
Presence of intact immune system Technical hurdlesfor monitoring tumor response in internal organs
All cell types within tumor are of mouse origin Low throughput and high investment
Features of tumor microenvironment, including stromal and vascular cells, and immune system components
*

=low

$

=low

$$

=intermediate cost

$$$

=high cost.

Up to 1 y to observe metastases.

Adapted with permission of (21).