3--methoxy-4--nitroflavone and geldanamycin

Dioxin, a potent tumor promoter, activates the aryl hydrocarbon receptor (AHR), a ligand-activated transcription factor belonging to the basic helix-loop-helix-PAS family, to enhance tumorigenesis via unknown mechanisms. We undertook this study to determine the mechanisms underlying the impact of dioxin on cell fate, in particular senescence that occurs in normal human cells and is considered to play important tumor suppressive function. We have previously shown that in primary human keratinocytes, dioxin attenuates senescence while retaining the proliferative capacity and represses expression of the tumor suppressors, p16(INK4a) and p53. Here, we show that repression of p16(INK4a) and p53 transcriptional activity by dioxin absolutely requires the AHR and is accompanied by promoter methylation. Furthermore, dioxin alone is sufficient to immortalize normal human keratinocytes. Our data introduce a previously unrecognized regulatory pathway, that of the AHR, that impacts senescence. More importantly, this is the first report of a tumor promoter capable of inhibiting senescence in a receptor mediated manner and introduces a novel mechanism by which this carcinogen may contribute to human malignancies.

Topics: Aryl Hydrocarbon Receptor Nuclear Translocator; Benzoquinones; Cell Line, Transformed; Cellular Senescence; Cyclin-Dependent Kinase Inhibitor p16; DNA; DNA Methylation; DNA-Binding Proteins; Down-Regulation; Flavonoids; Gene Silencing; Humans; Keratinocytes; Lactams, Macrocyclic; Polychlorinated Dibenzodioxins; Promoter Regions, Genetic; Quinones; Receptors, Aryl Hydrocarbon; RNA, Small Interfering; Transcription Factors; Transcription, Genetic; Tumor Suppressor Protein p53