okadaic-acid and cholesteryl-sulfate

okadaic-acid has been researched along with cholesteryl-sulfate* in 1 studies

Other Studies

1 other study(ies) available for okadaic-acid and cholesteryl-sulfate

ArticleYear
Alterations in cholesterol sulfate and its biosynthetic enzyme during multistage carcinogenesis in mouse skin.
    The Journal of investigative dermatology, 1998, Volume: 111, Issue:6

    Recent evidence suggests that cholesterol sulfate may be an important second messenger involved in signaling epidermal differentiation in skin. The activity of cholesterol sulfotransferase (Ch-ST) is increased during squamous differentiation of keratinocytes and is believed to be a marker enzyme for terminal differentiation. The primary objective of this study was to examine changes in levels of cholesterol sulfate (CS) and activity of its biosynthetic enzyme, Ch-ST, during multistage carcinogenesis in mouse skin. Using SENCAR mice, we determined the activity of Ch-ST in normal epidermis, in tumor promoter-treated epidermis, in epidermis during wound healing, and in mouse skin tumors generated by initiation-promotion regimens. A single topical application of tumor promoters led to significantly elevated levels of Ch-ST activity and of CS. Epidermal Ch-ST activity was also elevated during wound healing. Dramatic increases in CS levels and in the activity of Ch-ST were found in nearly all of the papillomas and squamous cell carcinomas examined. The increased levels of CS and activity of Ch-ST in tumor promoter-treated epidermis were accompanied by increased transglutaminase-I activity. In contrast, transglutaminase I activity was not elevated in primary papillomas or squamous cell carcinomas. Finally, Ch-ST activity was significantly elevated in the epidermis of newborn HK1.ras transgenic mice, whereas transglutaminase I activity did not correlate with Ch-ST activity in these mice. These results demonstrate that diverse tumor-promoting stimuli all produce elevated CS levels and Ch-ST activity and that CS levels and Ch-ST activity were constitutively elevated in both papillomas and squamous cell carcinomas. The data also suggest a mechanism for upregulation of Ch-ST in skin tumors involving activation/upregulation of Ha-ras.

    Topics: Administration, Topical; Animals; Anthracenes; Anticarcinogenic Agents; Carcinogens; Cell Differentiation; Cell Division; Cholesterol Esters; Dehydroepiandrosterone Sulfate; Epidermis; Female; Keratinocytes; Mice; Mice, Inbred SENCAR; Mice, Transgenic; Okadaic Acid; Skin Neoplasms; Sulfotransferases; Tetradecanoylphorbol Acetate; Transglutaminases; Wound Healing

1998