Ret transgenic mouse model of spontaneous skin melanoma: focus on regulatory T cells

Ret transgenic mouse model of skin malignant melanoma is characterized by the overexpression of the human ret transgene in melanin-containing cells. Transgenic mice spontaneously develop skin tumors with metastases in lymph nodes, lungs, liver, brain, and the bone marrow. Tumor lesions show typical...

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Bibliographic Details
Main Authors: Umansky, Viktor (Author) , Sevko, Alexandra (Author)
Format: Article (Journal)
Language:English
Published: 8 April 2013
In: Pigment cell & melanoma research
Year: 2013, Volume: 26, Issue: 4, Pages: 457-463
ISSN:1755-148X
DOI:10.1111/pcmr.12104
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1111/pcmr.12104
Verlag, lizenzpflichtig, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1111/pcmr.12104
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Author Notes:Viktor Umansky and Alexandra Sevko
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Summary:Ret transgenic mouse model of skin malignant melanoma is characterized by the overexpression of the human ret transgene in melanin-containing cells. Transgenic mice spontaneously develop skin tumors with metastases in lymph nodes, lungs, liver, brain, and the bone marrow. Tumor lesions show typical melanoma morphology and express melanoma-associated antigens. Although transgenic mice demonstrate an accumulation of melanoma antigen-specific memory and effector T cells, their anti-tumor effects could be blocked by highly immunosuppressive leukocytes enriched in the tumor microenvironment and in the periphery. Here, we discuss the role of one of the most potent immunosuppressive subset, regulatory T cells, in the melanoma progression in this model.
Item Description:Gesehen am 17.02.2022
Physical Description:Online Resource
ISSN:1755-148X
DOI:10.1111/pcmr.12104