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Medicine and Health Sciences Commons

Open Access. Powered by Scholars. Published by Universities.®

Oncology

Thomas Jefferson University

Department of Biochemistry and Molecular Biology Faculty Papers

Animal cell; animal experiment; animal model; Article; basement membrane; carcinogenesis; cell proliferation; controlled study; epidermis; genotype; growth inhibition; hair follicle; hyperplasia; in vitro study; in vivo study; keratinocyte; mouse; nonhuman; protein expression; protein phosphorylation; protein protein interaction; skin cancer; tumor growth; tumor volume; upregulation

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Full-Text Articles in Medicine and Health Sciences

Crosstalk Between Desmoglein 2 And Patched 1 Accelerates Chemical-Induced Skin Tumorigenesis., Donna M Brennan-Crispi, Claudia Hossain, Joya Sahu, Mary Brady, Natalia A Riobo, M G Mahoney Apr 2015

Crosstalk Between Desmoglein 2 And Patched 1 Accelerates Chemical-Induced Skin Tumorigenesis., Donna M Brennan-Crispi, Claudia Hossain, Joya Sahu, Mary Brady, Natalia A Riobo, M G Mahoney

Department of Biochemistry and Molecular Biology Faculty Papers

Aberrant activation of Hedgehog (Hh) signaling is causative of BCCs and has been associated with a fraction of SCCs. Desmoglein 2 (Dsg2) is an adhesion protein that is upregulated in many cancers and overexpression of Dsg2 in the epidermis renders mice more susceptible to squamous-derived neoplasia. Here we examined a potential crosstalk between Dsg2 and Hh signaling in skin tumorigenesis. Our findings show that Dsg2 modulates Gli1 expression, in vitro and in vivo. Ectopic expression of Dsg2 on Ptc1+/lacZ background enhanced epidermal proliferation and interfollicular activation of the Hh pathway. Furthermore, in response to DMBA/TPA, the Dsg2/Ptc1+/lacZ mice developed squamous …