To know the biological basis allowing the use of Ag-NOR protein expres
sion as proliferation marker in human malignancies, the relationship b
etween cell cycle and amount of Ag-NOR protein was analysed. The quant
ification of the two major Ag-NOR proteins, nucleolin and protein B23,
was performed in exponentially growing, serum-deprived, and cell-cycl
e stimulated cells. Expression of nucleolin was low in serum-deprived
cells and increased mostly in S phase during cell-cycle stimulation. C
onversely, expression of protein B23 was slightly repressed in serum-d
eprived cells, and increased progressively until G(2) phase during cel
l-cycle stimulation. The accumulation of nucleolin and protein B23 in
G(2) compared to G(1) was demonstrated using sorted phase-specific cel
ls. In G(0), cells sorted according to their very low RNA content, and
the amount of Ag-NOR proteins was half of that found in G(1) cells, n
ucleolin being only weakly detectable. Therefore, the expression of nu
cleolin increased between G(0)-G(1) and G(1)-S phases. These data supp
ort the hypothesis that quantification of Ag-NOR proteins is an estima
tion of the percentage of cells in each cell cycle phase because their
amount is high in S-G(2) and low in G(1) phases. (C) Wiley-Liss, Inc.