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A novel mechanism of skin tumor promotion involving interferon‐gamma (IFNγ)/signal transducer and activator of transcription‐1 (Stat1) signaling
Author(s) -
Bozeman Ronald,
Abel Erika L.,
Macias Everardo,
Cheng Tianyi,
Beltran Linda,
DiGiovanni John
Publication year - 2015
Publication title -
molecular carcinogenesis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.254
H-Index - 97
eISSN - 1098-2744
pISSN - 0899-1987
DOI - 10.1002/mc.22132
Subject(s) - biology , stat protein , tumor promotion , stat1 , downregulation and upregulation , signal transduction , cancer research , transcription factor , phosphorylation , carcinogenesis , microbiology and biotechnology , immunology , stat3 , biochemistry , gene
The current study was designed to explore the role of signal transducer and activator of transcription 1 (Stat1) during tumor promotion using the mouse skin multistage carcinogenesis model. Topical treatment with both 12‐ O ‐tetradecanoylphorbol‐13‐acetate (TPA) and 3‐methyl‐1,8‐dihydroxy‐9‐anthrone (chrysarobin or CHRY) led to rapid phosphorylation of Stat1 on both tyrosine (Y701) and serine (S727) residues in epidermis. CHRY treatment also led to upregulation of unphosphorylated Stat1 (uStat1) at later time points. CHRY treatment also led to upregulation of interferon regulatory factor 1 (IRF‐1) mRNA and protein, which was dependent on Stat1. Further analyses demonstrated that topical treatment with CHRY but not TPA upregulated interferon‐gamma (IFNγ) mRNA in the epidermis and that the induction of both IRF‐1 and uStat1 was dependent on IFNγ signaling. Stat1 deficient (Stat1 −/− ) mice were highly resistant to skin tumor promotion by CHRY. In contrast, the tumor response (in terms of both papillomas and squamous cell carcinomas) was similar in Stat1 −/− mice and wild‐type littermates with TPA as the promoter. Maximal induction of both cyclooxygenase‐2 and inducible nitric oxide synthase in epidermis following treatment with CHRY was also dependent on the presence of functional Stat1. These studies define a novel mechanism associated with skin tumor promotion by the anthrone class of tumor promoters involving upregulation of IFNγ signaling in the epidermis and downstream signaling through activated (phosphorylated) Stat1, IRF‐1 and uStat1. © 2014 Wiley Periodicals, Inc.