Tw. Chan et al., Inhibition of insulin-like growth factor signaling pathways in mammary gland by pure antiestrogen ICI 182,780, CLIN CANC R, 7(8), 2001, pp. 2545-2554
The antiestrogens ICI 182,780 (ICI) and tamoxifen are clinically useful in
the treatment of estrogen receptor-positive breast tumors. We assessed the
in vivo effects of ICI, tamoxifen, and estradiol on the insulin-like growth
factor (IGF) signaling pathway in the rat mammary gland. ICI significantly
decreased the size of the lobular structures, Ki-67 labeling index, and in
sulin-like growth factor binding protein (IGFBP)-2 and IGFBP-5 gene express
ion. Treatment of rats with 1, 1.5, and 2 mg of ICI/kg body weight/week res
ulted in a 2-, 7-, and 8-fold increase in IGFBP-3 transcripts. High doses o
f ICI increased mammary IGF-1 gene expression by 2-fold (P < 0.01) but decr
eased IGF-IR and its autophosphorylation to similar to 30% of the control m
ammary gland. IRS-1, IRS-2, and c-Raf-1 levels in the ICI-treated mammary g
lands were approximately 30, 15, and 40% of controls, respectively. Basal p
hosphorylation of IRS-1, Akt-1, and the p85 subunit of phosphatidylinositol
3-kinase (PI-3K) were low but detectable after ICI treatment. Despite a si
gnificant reduction in levels of IGF-1R, IRS-1, and IRS-2 phosphorylation,
phospho p42/p44 MAPK levels were only slightly decreased. Tamoxifen-induced
growth inhibition was associated with slight stimulation of IGFBP-3 gene e
xpression and reduction in IRS-2 levels. Basal phosphorylation of IGF-IR, I
RS-1, and p85 subunit of PI-3K was decreased by tamoxifen. Estradiol-induce
d epithelial cell proliferation was associated with inhibition of IGFBP-3 g
ene expression, stimulation of IGFBP-2 gene expression, and increases in IG
F-1R, IRS-1, IRS-2, and c-Raf-1 levels. Although basal phosphorylation of I
GF-IR, IRS-1, IRS-2, Akt-1, and the p85 subunit of PI-3K was significantly
increased by estradiol, basal phospho p44/42 MAPK was significantly reduced
. The data indicate that in addition to their classic actions, antiestrogen
s have major effects on IGF signaling pathways.