We have investigated the effects exerted by sodium butyrate (NaBu) on
the growth and cell cycle perturbations of four human breast cancer ce
ll lines (MCF7, T47D, MDA-MB231 and BT20) with different steroid recep
tor profiles, Moreover, since one of the supposed mechanisms of action
for NaBu activity involves the induction of apoptosis, we have studie
d the effects of NaBu on DNA fragmentation by agarose gel electrophore
sis and flow cytometry. In all investigated cell lines, NaBu exerted a
time- and dose-dependent inhibition of growth and caused a maximum in
hibitory effect (85% to 90%) at the concentration of 2.5 mM. The inhib
ition was already evident after 3 days of treatment. The antiprolifera
tive effect of NaBu was associated with a persistent block of cells in
the G(2)M phase. The block was associated with apoptosis only in oest
rogen-receptor positive cell lines, The inhibiting effect of NaBu in h
ormone-dependent and independent cell lines and its ability to induce
apoptosis through a cell cycle perturbation in hormone-dependent cell
lines may have important implications in the treatment of human tumour
s including breast cancer.