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Insulin-like Growth Factor-I (IGF-I) and IGF-binding Proteins Blood Serum Levels in Women with Early- and Late-stage Breast Cancer: Mutual Relationship and Possible Correlations with Patients' Hormonal Status

Overview
Specialty Oncology
Date 1995 Jan 1
PMID 7593132
Citations 3
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Abstract

The pathogenesis and progression of breast cancer involve complex interactions between hormones and polypeptide growth factors such as insulin-like growth factor-I (IGF-I). IGF-I has been found in stromal fibroblasts derived from malignant and benign breast tissue and it is a mitogen for several breast cancer cell lines. It circulates bound to specific high-affinity binding proteins, which could act as either positive or negative modulators of tumorigenesis. This study has been addressed to characterize IGF-I and its binding proteins in the serum of 85 unselected patients with early breast cancer. The IGF-I concentration was assessed by radioimmunoassay of 69 out of 85 samples before and after dissociation of the IGF-I and IGF-binding protein (IGF-BP) complex whereas IGF-BP of all 85 sera were analyzed by Western ligand blotting; estradiol and progesterone were measured by radioimmunoassay in native serum samples. In our study no differences in IGF-I serum levels between pre- and post-menopausal patients were observed. Patients with higher estradiol and progesterone serum levels did not present different IGF-I concentrations compared to patients with lower serum levels. Furthermore, IGF-I median values were not found to depend on estrogen receptor (ER) status. A heterogeneous quali-quantitative molecular pattern of binding proteins was detected: IGF-BP3 and IGF-BP1 were the most and the least expressed respectively. No correlations between ER status, or parameters related to the hormonal status, and IGF-I or binding proteins expression were observed. No significant differences in IGF-I concentration and IGF-BP expression were observed between cancer patients and a control group matched for age and menopausal status. Finally, preliminary collection of 20 sera derived from patients with late breast cancer was analyzed for IGF-I and its binding proteins content.

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References
1.
Figueroa J, Yee D . The insulin-like growth factor binding proteins (IGFBPs) in human breast cancer. Breast Cancer Res Treat. 1992; 22(1):81-90. DOI: 10.1007/BF01833336. View

2.
Scott C, Martin J, BAXTER R . Rat hepatocyte insulin-like growth factor I and binding protein: effect of growth hormone in vitro and in vivo. Endocrinology. 1985; 116(3):1102-7. DOI: 10.1210/endo-116-3-1102. View

3.
Klapper D, Svoboda M, Van Wyk J . Sequence analysis of somatomedin-C: confirmation of identity with insulin-like growth factor I. Endocrinology. 1983; 112(6):2215-7. DOI: 10.1210/endo-112-6-2215. View

4.
RUDMAN D, Feller A, Nagraj H, Gergans G, Lalitha P, GOLDBERG A . Effects of human growth hormone in men over 60 years old. N Engl J Med. 1990; 323(1):1-6. DOI: 10.1056/NEJM199007053230101. View

5.
Elgin R, Busby Jr W, Clemmons D . An insulin-like growth factor (IGF) binding protein enhances the biologic response to IGF-I. Proc Natl Acad Sci U S A. 1987; 84(10):3254-8. PMC: 304847. DOI: 10.1073/pnas.84.10.3254. View