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PMID: 17610223 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Review

Signal transducer and activator of transcription 3 (Stat3) in epithelial carcinogenesis.

Molecular carcinogenesis ·Vol. 46 ·No. 8 ·2007-08-00 ·Pages 725-31

Kim DJ, Chan KS, Sano S, Digiovanni J

Abstract

Signal transducer and activator of transcription 3 (Stat3) is one of a family of cytoplasmic proteins that participate in normal cellular responses to cytokines and growth factors as transcription factors. Stat3 modulates various physiological functions including cell survival, cell-cycle regulation, and angiogenesis through regulation of gene expression, and its constitutive activation is associated with a number of human epithelial cancers. Recent studies with skin-specific gain and loss of Stat3 function transgenic mice have shown that Stat3 plays critical roles in skin carcinogenesis. Multistage skin carcinogenesis bioassays performed with these transgenic mice clearly demonstrate that Stat3 is required for both tumor initiation and promotion through regulation of genes involved in survival and proliferation, respectively. Stat3 also plays a role in malignant progression of skin tumors by regulating genes that are involved in angiogenesis and invasion. Further studies have revealed that Stat3 plays a critical role in epidermal cell proliferation and survival following exposure to ultraviolet B (UVB) irradiation. In addition, Stat3 is constitutively active in UVB-induced skin tumors from both mice and humans. Collectively, these studies suggest that Stat3 may be a potential target for both the prevention and treatment of human epithelial cancers including skin cancer.

MeSH Terms
Animals Cell Transformation, Neoplastic Epidermis/drug effects,metabolism,pathology Humans Neoplasms, Glandular and Epithelial/etiology,metabolism Neoplasms, Radiation-Induced/etiology,metabolism STAT3 Transcription Factor/metabolism Skin Neoplasms/etiology,metabolism Ultraviolet Rays
Chemicals
STAT3 Transcription Factor
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Kim Dae Joon
Department of Carcinogenesis, The University of Texas M.D. Anderson Cancer Center, Science Park--Research Division, Smithville, Texas 78957, USA.
Chan Keith S
Sano Shigetoshi
Digiovanni John
Article Info
Journal
Molecular carcinogenesis
Abbr.
Mol Carcinog
ISSN
0899-1987
Published
2007-08-00
Pages
725-31
Language
English
Region
United States
NLM ID
8811105
Subset
IM
Grants
NCI NIH HHS · CA76520 · United States
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