Table 4.
Mice Identification |
Main Features | Melanoma Research Applications | References |
---|---|---|---|
Nude (nu/nu) | Athymic Homozygous for mutation Foxn1nu T cell deficient Hairless Cell line engraftment |
Pathophysiological mechanisms Novel therapies/therapy resistance Nano-based therapeutic approaches Prognostic biomarkers and molecular imaging |
[213,214,215,216,217,218,219] |
SCID | Homozygous for the spontaneous mutation Prkdcscid T and B cell deficient Cell line/tumor engraftment |
Pathophysiological mechanisms Biodistribution studies |
[220,221,222,223] |
NOD/SCID | Homozygous for the spontaneous mutation Prkdcscid T and B cell deficient Impaired function of macrophages, DC and NK cells Cell line/tumor engraftment |
Pathophysiological mechanisms Gene therapy Adjuvant therapy for brain metastasis Discovery of novel therapeutic targets |
[224,225,226,227] |
NSG | NOD/SCID IL2rgnull T and B cell deficient Impaired function of macrophages and DC Lack of NK cells Enhanced tumor engraftment |
Pathophysiological mechanisms Therapy resistance Novel therapies/combination therapy Chemoprevention Development of imaging probes Biodistribution studies Identification of cell subpopulations |
[217,226,228,229,230,231,232,233,234,235] |
hu-NSG | NSG with humanized immune system induced by CD34+ HSC or PBMC | Prediction of patients’ response to immunotherapy Imaging of therapeutic targets Therapy resistance |
[236,237,238,239] |
DC: dendritic cells; HSC: hematopoietic stem cells; hu-NSG: humanized NSG; IL2rg: interleukin-2 receptor gamma chain; NOD/SCID: nonobese diabetic-severe combined immunodeficiency; NK cells: natural killer cells; NSG: NOD/SCID gamma; PBMC: peripheral blood mononuclear cells; Prkdc: protein kinase DNA-activated catalytic polypeptide.