Aims-An increased concentration of insulin-like growth factor 1 (IGF-1) is
an independent risk factor for premenopausal breast cancer. Tamoxifen is th
ought initially to reduce concentrations of IGF-1 and increase concentratio
ns of the IGF binding proteins. The aim of this study was to compare concen
trations of IGF-1, IGF binding protein 1 (IGF-BP1), and IGF-BP3 in patients
with breast cancer (n = 14) with those seen in control subjects (n = 23) a
nd to assess the effect of tamoxifen on IGF status in these patients.
Methods-Non-fasting blood samples were collected from patients with breast
cancer before surgery and after nine, 18, and 27 months of tamoxifen treatm
ent. The baseline concentrations were compared with those of age and sex ma
tched healthy control subjects.
Results-IGF-1, IGF-BP3, and IGF-BP1 concentrations were not significantly d
ifferent in cases and controls. Tamoxifen treatment significantly increased
IGF-BP1 after IS and 27 months (baseline: mean, 21.6 ng/ml; SD, 16.6; 18 m
onths; mean, 52.0 ng/ml; SD, 41.8; p = 0.019; 27 months: mean, 40.7 ng/ml;
SD, 24.9; p = 0.043) and IGF-BP3 after nine, IS, and 27 months (baseline: m
ean, 3119 ng/ml; SD, 507; nine months: mean, 3673 ng/ml; SD, 476; p = 0.004
; 18 months: mean, 3445 ng/ml; SD, 634; p = 0.034; 27 months: 3409 ng/ml; S
D, 501; p = 0.043) when compared with baseline values. IGF-1 was not altere
d significantly from baseline at any time point. However, the IGF-1 to IGF-
BP3 ratio was significantly decreased at both nine and 18 months (baseline:
mean, 0.058; SD, 0.014; nine months: mean, 0.039; SD, 0.008; p = 0.033; 18
months: mean, 0.044; SD, 0.012; p = 0.01). This ratio was not significantl
y different from baseline at 27 months (mean, 0.054; SD, 0.01; p = 0.08).
Conclusions-Tamoxifen increases IGF-BP3 and IGF-BP1 concentrations. It also
decreases the IGF-1 to IGF-BP3 ratio but this effect may be limited after
long term use. Longer follow up, with larger numbers of patients, should de
termine when, and for how long, tamoxifen can reduce circulating IGF-1.