Role of insulin like growth factors in steroid modulated proliferation
Browse by author
Lookup NU author(s): Professor Bruce Westley, Dr Felicity May
Full text for this publication is not currently held within this repository. Alternative links are provided below where available.
The mechanism by which steroids influence cell proliferation is poorly understood although an understanding of this process might facilitate the development of strategies to modulate the tissue-specific activity of steroid hormones. In this article, the evidence that steroid hormones interact with the insulin-like growth factor (IGF) signal transduction pathway is reviewed for three different tissues. In osteoblasts, oestradiol stimulates the production of IGF-I which appears to act as an autocrine growth factor. In uterine tissue, oestradiol increases the synthesis of IGF-I in the stroma which then modulates the proliferation of epithelial cells although there is also evidence that oestradiol can modulate the sensitivity of uterine epithelial cells to IGFs. In breast cancer, oestrogens may increase IGF-II synthesis in epithelial cells, increase the sensitivity of breast cancer cells to IGFs (possibly by modulating type I IGF receptor levels) as well as resulting components of the IGF signal transduction pathway resulting in induction of immediate early genes. There therefore appears to be a variety of ways in which oestradiol interact with the IGF signal transduction pathway and these may be applicable to other malignant and normal tissues and other groups of steroid hormones.
Author(s): Westley BR, May FEB
Publication type: Review
Publication status: Published
Journal: The Journal of Steroid Biochemistry and Molecular Biology
Year: 1994
Volume: 51
Issue: 1-2
Pages: 1-9
Print publication date: 01/10/1994
ISSN (print): 0960-0760
ISSN (electronic): 1879-1220
URL: http://dx.doi.org/10.1016/0960-0760(94)90109-0
DOI: 10.1016/0960-0760(94)90109-0