“…To this end, MDA-MB-231 cells were selected because FK866 was found to minimally affect their growth (24,20, and 27% growth inhibition at 72 h in response to 10 nM, 100 nM, and 1 M FK866, respectively), while, at the same time, reducing intracellular NAD ϩ by more than 50%. Conversely, BT549 and MDA-MD-468 were more sensitive to the growth-inhibiting effects of this drug (for BT549, 51, 54, and 67% growth inhibition at 72 h in response to 10 nM, 100 nM, and 1 M FK866, respectively; for MDA-MD-468, 32, 38, and 41% growth inhibition at 72 h in response to 10 nM, 100 nM, and 1 M FK866, respectively) and, therefore, were not selected for these experiments.…”