INSULIN-LIKE GROWTH-FACTOR BINDING-PROTEIN-3 (IGF-BP3) INHIBITS ESTROGEN-STIMULATED BREAST-CANCER CELL-PROLIFERATION

被引:68
作者
PRATT, SE [1 ]
POLLAK, MN [1 ]
机构
[1] JEWISH GEN HOSP,MONTREAL H3T 1E2,PQ,CANADA
关键词
D O I
10.1006/bbrc.1994.1041
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have recently demonstrated that exposure of MCF7 cells to antiestrogens in vitro results in both accumulation of IGF-BP3 in media and reduced mitogenic responsivity to IGFs (Cancer Res. 53:5193-5198). We show here that MCF7 cell proliferation in steroid stripped, serum containing media is significantly attenuated by rhIGF-BP3 (p<0.05), with a maximal 40% inhibition of serum stimulated growth achieved by 6.25 nM IGF-BP3. 10-10M estradiol (E2) significantly stimulated MCF7 proliferation, and co-incubation of estrogen containing cultures with 50 nM IGF-BP3 resulted in significant attenuation of the estrogen-stimulated proliferation ([3H]thymidine incorporation: E2, 147 ± 18% of control; E2 + IGF-BP3, 111 ± 18% of control, p<0.05). These resuits demonstrate antagonism of steroid stimulated proliferation by an IGF binding protein and are compatible with the hypothesis that antiestrogen-induced accumulation of IGF-BP3 in the conditioned media of MCF7 cells contributes to the cytostatic action of these drugs. © 1994 Academic Press, Inc.
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页码:292 / 297
页数:6
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