Development of an in vitro analogue of initiated mouse epidermis to study tumor promoters and antipromoters

Henry Hennings, Victor A. Robinson, Delores M. Michael, George Pettit, Reinhard Jung, Stuart H. Yuspa

Research output: Contribution to journalArticle

36 Citations (Scopus)

Abstract

To facilitate the study of skin tumor promotion, a cell culture model system with characteristics analogous to initiated mouse epidermis was established. Cells of the keratinocyte cell line 308, derived from adult mouse skin initiated with 7,12-dimethylbenz[a]anthracene, display the initiated phenotype, since papillomas are produced when the cells are grafted to the backs of athymic mice. Coculture of a small number of these initiated cells with confluent normal primary keratinocytes resulted in the inhibition of growth of colonies of 308 cells. Addition of fresh keratinocytes weekly was required to sustain the inhibition for 3-4 weeks. Inhibition of 308 cell colonies required culture medium with a calcium concentration of 1.2 mM; normal keratinocytes did not inhibit 308 cells in medium with 0.05 mM calcium. Growth of 308 cells was not inhibited by coculture with confluent fibroblasts or by 1.2 mM calcium medium conditioned by either keratinocytes or fibroblasts. During continuous exposure of the cocultures to tumor promoters, 308 cell colonies became apparent within 2-3 weeks. A limited number of promoters were tested in this model system and 12-O-tetradecanoylphorbol-13-acetate, 12-O-retinoylphorbol-13-acetate, mezerein, and benzoyl peroxide were all active. The number of colonies which developed during promoter exposure in cocultures showed a dose-response curve which differed from the dose-response curve for stimulation of growth of 308 colonies in the absence of normal keratinocytes. Simultaneous treatment with 12-O-tetradecanoylphorbol-13-acetate and known inhibitors of skin tumor promotion, such as retinoic acid, fluocinolone acetonide, and bryostatin 1, blocked colony formation of 308 cells in cocultures but not in cultures with only 308 cells. In this model system, the actions of promoters and inhibitors both appear to be mediated by normal keratinocytes.

Original languageEnglish (US)
Pages (from-to)4794-4800
Number of pages7
JournalCancer Research
Volume50
Issue number15
StatePublished - Aug 1 1990

Fingerprint

Epidermis
Carcinogens
Keratinocytes
Coculture Techniques
Tetradecanoylphorbol Acetate
Calcium
Skin
Fluocinolone Acetonide
Growth
Fibroblasts
Benzoyl Peroxide
In Vitro Techniques
Papilloma
Conditioned Culture Medium
Tretinoin
Nude Mice
Culture Media
Neoplasms
Cell Culture Techniques
Cell Count

ASJC Scopus subject areas

  • Cancer Research
  • Oncology

Cite this

Hennings, H., Robinson, V. A., Michael, D. M., Pettit, G., Jung, R., & Yuspa, S. H. (1990). Development of an in vitro analogue of initiated mouse epidermis to study tumor promoters and antipromoters. Cancer Research, 50(15), 4794-4800.

Development of an in vitro analogue of initiated mouse epidermis to study tumor promoters and antipromoters. / Hennings, Henry; Robinson, Victor A.; Michael, Delores M.; Pettit, George; Jung, Reinhard; Yuspa, Stuart H.

In: Cancer Research, Vol. 50, No. 15, 01.08.1990, p. 4794-4800.

Research output: Contribution to journalArticle

Hennings, H, Robinson, VA, Michael, DM, Pettit, G, Jung, R & Yuspa, SH 1990, 'Development of an in vitro analogue of initiated mouse epidermis to study tumor promoters and antipromoters', Cancer Research, vol. 50, no. 15, pp. 4794-4800.
Hennings, Henry ; Robinson, Victor A. ; Michael, Delores M. ; Pettit, George ; Jung, Reinhard ; Yuspa, Stuart H. / Development of an in vitro analogue of initiated mouse epidermis to study tumor promoters and antipromoters. In: Cancer Research. 1990 ; Vol. 50, No. 15. pp. 4794-4800.
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