Granulocyte-macrophage colony-stimulating factor (GM-CSF) is expressed in mouse skin in response to tumor-promoting agents and modulates dermal inflammation and epidermal dark cell numbers
| Autor: | Marian L. Miller, Alvaro Puga, K B Vasunia, C S Baxter |
|---|---|
| Rok vydání: | 1994 |
| Předmět: |
Cancer Research
medicine.medical_specialty medicine.medical_treatment Molecular Sequence Data Retinoic acid Gene Expression Mice Inbred Strains Biology Mice chemistry.chemical_compound Internal medicine medicine Animals RNA Messenger DNA Primers Skin Inflammation Base Sequence integumentary system Epidermis (botany) Growth factor Granulocyte-Macrophage Colony-Stimulating Factor General Medicine Hyperplasia medicine.disease Cytokine Endocrinology medicine.anatomical_structure chemistry Receptors Granulocyte-Macrophage Colony-Stimulating Factor Carcinogens Cancer research Phorbol Female Tumor promotion Keratinocyte |
| Zdroj: | Carcinogenesis. 15:653-660 |
| ISSN: | 1460-2180 0143-3334 |
| Popis: | In mouse dorsal skin multistage carcinogenesis models, tumor promotion can be mediated by chemical agents, but also by wounding or abrasion of the epidermis, suggesting that endogenous growth factors mediate this process. Granulocyte-macrophage colony-stimulating factor (GM-CSF) is one such factor that has been reported to be produced by keratinocytes in vitro, and has been suggested both to stimulate keratinocyte proliferation, and also to be a chemoattractant for neutrophils and macrophages. In this study we examined the expression and function of GM-CSF in mouse skin following the application of tumor-promoting agents. Both single and multiple applications of 12-O-tetradecanoylphorbol-13-acetate (TPA) resulted in accumulation of GM-CSF mRNA in the epidermis. Various phorbol and non-phorbol ester tumor promoters were found to induce increases in epidermal GM-CSF mRNA levels commensurate with their relative tumor promoting capabilities. Fluocinolone acetonide (FA) and tosyl phenylalanine chloromethyl ketone (TPCK), inhibitors of tumor promotion, inhibited tumor promoter-mediated GM-CSF accumulation, whereas all-trans-retinoic acid (RA) enhanced the TPA-induced increase. The retinoic acid analogue RO-109359 which, unlike RA, does not have tumor promoting activity per se, inhibited the TPA-induced increase in epidermal GM-CSF mRNA levels. When an antibody specific to GM-CSF was administered prior to TPA, the promoter-induced dermal inflammation and increase in epidermal dark cell number were reduced, yet promoter-induced epidermal hyperplasia was not. These findings implied that elevation of GM-CSF levels plays an important role in chemically-mediated mouse skin tumor promotion and principally via effects on promoter-induced inflammation and increased epidermal dark cell number. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
|