Cytotoxicity of 4-hydroxyanisole and tyrosinase activity in variant cell lines of B16 melanoma.

Abstract

The melanocytotoxic effects of 4-hydroxyanisole (4-OHA) are thought to depend upon its conversion to toxic oxidation products by the enzyme tyrosinase. In this study, the cytotoxicity of 4-OHA was examined in different B16 melanoma cell lines that show varying levels of tyrosinase and after stimulation by melanocyte-stimulating hormone (MSH) and all-trans-retinoic acid (RA). 4-OHA decreased cell survival of three melanotic and one amelanotic cell line in culture, but the effect was unrelated to their tyrosinase activity or the subcellular localization of the enzyme. Although stimulation of tyrosinase activity with RA enhanced the cytotoxicity of 4-OHA, no similar enhancement occurred with alpha-MSH. It appears that there is no relationship between the cytotoxic effects of 4-OHA and intracellular tyrosinase and the enhancement of its cytotoxicity by RA may well be related to the antiproliferative effects of the retinoid.

• Authors: A J Thody, I Oliver, G V Sherbet
• Journal: European journal of cancer & clinical oncology (Eur J Cancer Clin Oncol) Vol. 24 Issue 12 Pg. 1879-84 (Dec 1988) ISSN: 0277-5379 [Print] England
• PMID: 2851444 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Anisoles
• Tretinoin
• mequinol
• Melanocyte-Stimulating Hormones
• Ditiocarb
• Catechol Oxidase
• Monophenol Monooxygenase

Topics

• Animals
• Anisoles (pharmacology)
• Catechol Oxidase (metabolism)
• Cell Survival (drug effects)
• Ditiocarb (pharmacology)
• Melanocyte-Stimulating Hormones (pharmacology)
• Melanoma (enzymology)
• Mice
• Monophenol Monooxygenase (metabolism)
• Tretinoin (pharmacology)
• Tumor Cells, Cultured (drug effects, metabolism)