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Although abundant in tumor tissue, mast cells have no effect on immunological micro‐milieu or growth of HPV‐induced or transplanted tumors
Abstract
High numbers of mast cells populate the stroma of many types of neoplasms, including human papilloma virus-induced benign and malignant tumors in man and mouse. Equipped with numerous pattern recognition receptors and capable of executing important pro-inflammatory responses, mast cells are considered innate sentinels that significantly impact tumor biology. Mast cells were reported to promote human papilloma virus (HPV)-induced epithelial hyperproliferation and neo-angiogenesis in an HPV-driven mouse model of skin cancer. We analyzed HPV-induced epithelial hyperplasia and squamous cell carcinoma formation, as well as growth of tumors inoculated into the dermis, in mice lacking skin mast cells. Unexpectedly, the absence of mast cells had no effect on HPV-induced epithelial growth or angiogenesis, on growth kinetics of inoculated tumors, or on the immunological tumor micro-milieu. Thus, the conspicuous recruitment of mast cells into tumor tissues cannot necessarily be equated with important mast cell functions in tumor growth.
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“Finally, several mouse studies have found that the absence of mast cells has no effect on skin carcinogenesis or the growth of subcutaneously inoculated melanoma. 231 , 232 , 233”
From Mast cell ontogeny: From fetal development to life‐long health and disease (2023) · cites this paper as [231]
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“Indeed, subcutaneous growth of B16 melanoma is unaffected in Mcpt5‐Cre:RosaDTA mice, 231 , 232 which lack all mast cells in the skin.”
From Mast cell ontogeny: From fetal development to life‐long health and disease (2023) · cites this paper as [231]
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Mast cell ontogeny: From fetal development to life‐long health and disease
Chia, S. L., Kapoor, S., Carvalho, C., Bajénoff, M., & Gentek, R. (2023) · Immunological Reviews · doi:10.1111/imr.13191 · Cited by 60
Metadata
- Authors
- Ghouse, S. M., Polikarpova, A., Muhandes, L., Dudeck, J., Tantcheva-Poór, I., Hartmann, K., Lesche, M., Dahl, A., Eming, S., Müller, W., Behrendt, R., & Roers, A.
- Venue
- Cell Reports
- Publisher
- Elsevier BV
- Published
- 2018-01
- Volume
- 22
- Issue
- 1
- Pages
- 27-35
- ISSN
- 2211-1247
- Cited by
- 20
- References
- 1
- Language
- en
- Licence
- Funders
- Deutsche Forschungsgemeinschaft (RO2133/7, RO2133/3, RO2133/4)
- Seventh Framework Programme (317445)
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