Auraptene is being investigated for its chemopreventive effects in many models of
cancer including skin, colon, prostate, and breast. Many mechanisms of action including anti-inflammatory, antiproliferative, and antiapoptotic effects are being suggested for the chemopreventive properties of
auraptene. We have previously shown in the N-
methylnitrosourea induced mammary
carcinogenesis model that dietary
auraptene (500 ppm) significantly delayed
tumor latency. The delay in time to
tumor corresponded with a significant reduction in
cyclin D1 protein expression in the
tumors. Since
cyclin D1 is a major regulator of cell cycle, we further studied the effects of
auraptene on cell cycle and the genes related to cell cycle in MCF-7 cells. Here we show that
auraptene significantly inhibited
IGF-1 stimulated S phase of cell cycle in MCF-7 cells and significantly changed the transcription of many genes involved in cell cycle.