AI Article Synopsis

  • Insulin-like growth factors (IGF-I and IGF-II) play a role in mammary gland development and may contribute to breast cancer, but their interactions with breast epithelial cells are not fully understood.
  • In experimental conditions without serum, human breast epithelial cells (HBEC) showed increased growth in response to IGF-I and IGF-II, and this growth was enhanced when combined with epidermal growth factor (EGF).
  • IGF binding protein-3 (IGFBP-3) was found to inhibit the growth stimulation from IGFs and EGF and also exhibited growth-inhibitory effects independently of IGF, highlighting its complex role in breast cell biology.

Article Abstract

Insulin-like growth factor-I (IGF-I) and insulin-like growth factor-II (IGF-II) are growth factors implicated in mammary gland development and are believed to be involved in breast cancer. However, the interactions between components of the IGF system and breast epithelial cells, which give rise to breast cancer, are not well understood. We have investigated the mitogenic properties of IGF-I, IGF-II, IGF binding protein-3 (IGFBP-3) and epidermal growth factor (EGF) on human breast epithelial cells (HBEC) in primary culture. We show that, under serum-free conditions, HBEC are stimulated to grow in response to IGF-I and IGF-II in a dose-dependent manner. IGF-I and EGF, a potent stimulator of HBEC growth in primary culture and also associated with breast cancer, appear to stimulate HBEC in a synergistic manner. IGFBP-3 inhibits the stimulation by IGF-I, IGF-II and IGF-I plus EGE In addition, it appears that IGFBP-3 has an inhibitory effect on HBEC growth that is IGF-independent. This study is the first to address the effects of IGF-I, IGF-II and IGFBP-3 alone and in combination with EGF on HBEC growth in primary culture. Characterizing the role of the IGF system in normal breast biology is significant because the system has been implicated in breast cancer and a number of the anti-estrogens used in treatment are believed to function through the IGF system.

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Source
http://dx.doi.org/10.1023/a:1019915101457DOI Listing

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