Effects of mammalian target of rapamycin inhibitors on cytokine production and differentiation in keratinocytes

Risk factors for the development of cutaneous squamous cell carcinoma (cSCC) include ultraviolet radiation and immunosuppression. In particular, solid organ transplant recipients show a high incidence of cSCC, depending on the immunosuppressive regimen. While azathioprine or calcineurin inhibitors i...

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Published inExperimental dermatology Vol. 25; no. 10; pp. 775 - 782
Main Authors DeTemple, Viola, Satzger, Imke, Walter, Antje, Schaper, Katrin, Gutzmer, Ralf
Format Journal Article
LanguageEnglish
Published Denmark Blackwell Publishing Ltd 01.10.2016
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ISSN0906-6705
1600-0625
DOI10.1111/exd.13079

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Summary:Risk factors for the development of cutaneous squamous cell carcinoma (cSCC) include ultraviolet radiation and immunosuppression. In particular, solid organ transplant recipients show a high incidence of cSCC, depending on the immunosuppressive regimen. While azathioprine or calcineurin inhibitors increase the risk of cSCC development, mammalian target of rapamycin (mTOR) inhibitors decreases this risk. At the moment, the mechanisms behind this protective effect of mTOR inhibitors are not fully understood. We evaluated effects of the mTOR inhibitors sirolimus and everolimus on keratinocytes, cSCC cell lines and an organotypic skin model in vitro in regard to proliferation, cytokine secretion and differentiation. We show that mTOR inhibitors block keratinocyte proliferation and alter cytokine and cytokeratin production: in particular, mTOR inhibition leads to upregulation of interleukin‐6 and downregulation of cytokeratin 10. Therefore, mTOR inhibitors have effects on keratinocytes, which could play a role in the pathogenesis of cSCC.
Bibliography:Bristol-Myers Squibb
GlaxoSmithKline
Amgen
ArticleID:EXD13079
Pfizer
Merck Serono
Novartis
istex:5571B2DEBB04BD7FDF41A7D407C96269B86B0ECC
Almirall Hermal
Roche Pharma
Janssen
Boehringer Ingelheim
LEO
Johnson&Johnson
ark:/67375/WNG-7VDH2VCG-N
MSD
Galderma
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ISSN:0906-6705
1600-0625
DOI:10.1111/exd.13079