Abstract
Steady-state levels of phosphatidyl inositol (Ptdlns) turnover are examined in MCF-7 human breast cancer cells in response to estradiol treatment. Elevated levels of Ptdlns are observed 12-24 h after estradiol treatment, occur at estradiol concentrations as low as 10-12 m, and are competitively blocked by the antiestrogen LY117018. MCF-7 cells secrete a transforming growth factor (TGF) α-like material which can partly replace estradiol in conferring tumorgen-icity in nude mice. We show that acute or chronic treatment of MCF-7 cells with TGFα results in elevated Ptdlns turnover and that chronic treatment increases growth rate. In contrast TGFβ is growth inhibitory and blocks estradiol-induced increases in Ptdlns turnover. A phosphatidyl inositol 4, 5-bisphos-phate specific phospholipase-C activity has been identified and is elevated in association with estradiol treatment. These data are consistent with estradiol-induced autocrine growth factors, including TGFα, acting through the Ptdlns turnover pathway as part of their mechanism of action.
Original language | English (US) |
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Pages (from-to) | 159-166 |
Number of pages | 8 |
Journal | Molecular Endocrinology |
Volume | 2 |
Issue number | 2 |
DOIs | |
State | Published - Aug 1988 |
ASJC Scopus subject areas
- Molecular Biology
- Endocrinology