We have shown that peptide YY, an endogenous gut hormone, and vitamin E suc
cinate (VES) inhibit pancreatic cancer cell growth in vitro. We hypothesize
d that PYY and VES would inhibit breast cancer cell viability regardless of
the hormone receptor status.
Human breast ZR-75 ductal carcinoma (estrogen receptor negative) and MCF-7
adenocarcinoma (estrogen receptor positive) cells were cultured and exposed
to VES (10 pg/ml), PYY (500 pmol), or both agents together, MTT assay was
performed at 24, 48, and 72 h to evaluate cell viability.
At every time interval, PYY and VES significantly inhibited cell growth com
pared to control. The effects of PYY were similar in magnitude to those of
VES, Combining the agents resulted in a significant additive inhibition of
growth with the greatest effect seen at 72 h.
We have shown that PYY and vitamin E inhibit in vitro growth of breast canc
er cells with variable hormone receptor status. When used in combination, t
he agents have a significant increase in effect. Further studies are ongoin
g to define the mechanism of action of these agents and to translate the ex
periments to an in vivo model. (C) 2000 Academic Press.