Carcinogenesis 1984-05-01

Non-promoting hyperplasiogenic agents do not mimic the effects of phorbol, 12-myristate, 13-acetate on terminal differentiation of normal and transformed human keratinocytes.

E K Parkinson, A Emmerson

Index: Carcinogenesis 5(5) , 687-90, (1984)

Full Text: HTML

Abstract

We have studied the effects of the potent tumour promoter phorbol, 12-myristate, 13-acetate (PMA) and two non-promoting hyperplasiogenic compounds ethyl phenylpropriolate (EPP) and the divalent cation ionophore A23187 on the terminal differentiation of normal and transformed human keratinocytes using the loss of cloning efficiency and the formation of cornified envelopes as markers of the differentiated state. PMA induced terminal differentiation in a far greater proportion of normal keratinocytes than it did in the squamous cell carcinoma line SCC-27 but EPP and the calcium ionophores A23187 and Br-X537A had no such differential effect, possibly explaining the poor promoting ability of the last three compounds.


Related Compounds

Related Articles:

Overexpression of three ubiquitin genes in mouse epidermal tumors is associated with enhanced cellular proliferation and stress.

1992-05-01

[Cell Growth Differ. 3(5) , 269-78, (1992)]

Changes in cytokeratins following treatment of hamster cheek pouch epithelia with hyperplastic or neoplastic agents.

1994-04-01

[J. Oral. Pathol. Med. 23(4) , 149-55, (1994)]

Benzoyl peroxide activation of protein kinase C activity in epidermal cell membranes.

1987-12-01

[Carcinogenesis 8(12) , 1871-4, (1987)]

Induction of ornithine decarboxylase in specific subpopulations of murine epidermal cells following multiple exposures to 12-O-tetradecanoylphorbol-13-acetate, mezerein and ethyl phenylpropriolate.

1992-01-01

[Carcinogenesis 13(1) , 51-6, (1992)]

Comparative histomorphometric changes in SENCAR mouse epidermis in response to multiple treatments with complete and stage-specific tumor promoting agents.

1989-10-01

[Carcinogenesis 10(10) , 1855-61, (1989)]

More Articles...