Experiments were conducted to determine the effect of beta-carotene on
human colon cancer cells in vitro. beta-Carotene solubilized in tetra
hydrofuran (THF) was determined to be cytotoxic for three different ce
ll lines: LS 180, SW 620, and HCT-15. The number of LS 180 and SW 620
cells surviving treatment with 2.9 mu M beta-carotene was significantl
y reduced relative to THF-treated cells, and a similar reduction was a
chieved in HCT-15 cells with use of 5.8 mu M beta-carotene. These conc
entrations are in the range achieved in serum of individuals supplemen
ted with beta-carotene at 30 mg/day. There was no beta-carotene cytoto
xicity in the concentration range that characterizes serum of unsupple
mented individuals. Vitamin E at >200 mu M was no cytotoxic and at hig
her concentrations slightly stimulated proliferation of all three cell
lines. Exposure of cells to vitamin E did not diminish the cytotoxici
ty of beta-carotene, suggesting that the toxic effect of beta-carotene
of exposure of cells to beta-carotene. interestingly, beta-carotene c
ytotoxicity decreased with increasing cell density. This density-depen
dent toxicity was attributable to a higher beta-carotene concentration
per cell for cells plated at lower. densities. Thus toxicity of p-car
otene for colon cancer cells is close, time, and cell density dependen
t and occurs in vitro at concentrations that can be achieved safely in
humans.