Journal Article

Vitamin D<sub>3</sub> receptor ablation sensitizes skin to chemically induced tumorigenesis

Glendon M. Zinser, John P. Sundberg and JoEllen Welsh

in Carcinogenesis

Volume 23, issue 12, pages 2103-2109
Published in print December 2002 | ISSN: 0143-3334
Published online December 2002 | e-ISSN: 1460-2180 | DOI:
Vitamin D3 receptor ablation sensitizes skin to chemically induced tumorigenesis

More Like This

Show all results sharing this subject:

  • Clinical Cytogenetics and Molecular Genetics


Show Summary Details


1,25-Dihydroxyvitamin D3 (1,25D3) is the biologically active form of vitamin D3 that interacts with the nuclear vitamin D3 receptor (VDR) to modulate gene expression in a tissue-specific fashion. 1,25D3 is a potent regulator of cell proliferation, differentiation and apoptosis in a variety of cell types, including keratinocytes. In these studies, we assessed the sensitivity of mice homozygous for a null allele of the VDR (VDR−/− mice) and their wild-type counterparts (VDR+/+ mice) to oral administration of the carcinogen 7,12-dimethylbenzanthracene (DMBA). Although the protocol was optimized for the induction of mammary tumors, 85% of VDR−/− mice developed persistent skin tumors within 60 days of carcinogen exposure. In VDR−/− mice exposed to DMBA, papillomas arose on all areas of the body, with an average tumor burden of 5.3 papillomas/mouse. No papillomas or any other skin lesions were observed in age- and sex-matched VDR+/+ mice dosed with DMBA and followed for 6 months. The majority (80%) of skin tumors that developed in VDR−/− mice were classified histologically as sebaceous, squamous or follicular papillomas. Other types of lesions, including basal cell carcinoma, hemangioma and melanotic foci, were occasionally observed in VDR−/− mice (but not in VDR+/+ mice) exposed to DMBA. Quantification of epidermal thickness and BrdU incorporation indicated that skin from VDR−/− mice exhibited hyperproliferation beginning at 7 weeks of age, which was exacerbated by DMBA treatment. Untreated aging VDR−/− mice did not exhibit tumor formation, but did develop a progressive skin phenotype characterized by thickened wrinkled skin, dermoid cysts and long curly nails. Together with previous reports that 1,25D3 inhibits papilloma formation induced by topical DMBA-TPA regimens, our observation of enhanced sensitivity of VDR−/− mice to chemically induced skin carcinogenesis offers compelling evidence that disruption of VDR signaling predisposes to neoplasia.

Keywords: 1,25D3, 1,25-dihydroxyvitamin D3; DMBA, 7,12-dimethylbenzanthracene; MPA, medroxyprogesterone acetate; ODC, ornithine decarboxylase; VDR, vitamin D3 receptor

Journal Article.  5756 words.  Illustrated.

Subjects: Clinical Cytogenetics and Molecular Genetics

Full text: subscription required

How to subscribe Recommend to my Librarian

Users without a subscription are not able to see the full content. Please, subscribe or login to access all content.