The polyacetylene falcarinol, isolated from carrots, has been shown to be protective against chemicallyinduced colon cancer development in rats, but the mechanisms are not fully understood. In this studyCaCo-2 cells were exposed to falcarinol (0.5-100
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M) and the effects on proliferation, DNA damage,and apoptosis investigated. Low-dose falcarinol exposure (0.5-10
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M) decreased expression of theapoptosis indicator caspase-3 concomitantly with decreased basal DNA strand breakage. Cellproliferation was increased (1-10
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M), whereas cellular attachment was unaffected by <10
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Mfalcarinol. At concentrations above 20
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falcarinol, proliferation of CaCo-2 cells decreased and thenumber of cells expressing active caspase-3 increased simultaneously with increased cell detachment.Furthermore, DNA single-strand breakage was significantly increased at concentrations above 10
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M falcarinol. Thus, the effects of falcarinol on CaCo-2 cells appear to be biphasic, inducing pro-proliferative and apoptotic characteristics at low and high concentrations of falcarinol, respectively.