The present study investigated the ability of two neuroblastoma cell l
ines (SK-N-SH, with one copy of N-myc, and SK-N-BE(2), with over 150 c
opies of N-myc) to recycle ascorbate by quantifying semidehydroascorba
te reductase and dehydroascorbate reductase activities. Both cell line
s expressed dehydroascorbate activity (SK-N-SH 28.4+/-9.8, SK-N-BE(2)
21.7+/-5.2 nmol/min/mg protein). Intracellular semidehydroascorbate ac
tivity was present only in SK-N-BE(2) cells (4.7+/-1.2 nmol/min/mg pro
tein). Extracellular ascorbate was regenerated by semidehydroascorbate
membrane activity, the activity of SK-N-BE(2) being twice that of SK-
N-SH cells. The present data may explain the ability of the tumor to p
rogress or regress through mechanisms involving both myc oncogene and
apoptosis.