agar and 4-hydroxyestradiol

agar has been researched along with 4-hydroxyestradiol* in 1 studies

Other Studies

1 other study(ies) available for agar and 4-hydroxyestradiol

ArticleYear
The estrogen antagonist ICI-182-780 does not inhibit the transformation phenotypes induced by 17-beta-estradiol and 4-OH estradiol in human breast epithelial cells.
    International journal of oncology, 2005, Volume: 26, Issue:2

    Prolonged unopposed estrogen exposure is a widely accepted risk factor in breast cancer development. However, the mechanisms through which estrogens induce breast carcinogenesis have not been definitively unraveled. For testing whether estrogens exert their transforming effects through a non-receptor-mediated mechanism, we have treated the spontaneously immortalized human breast epithelial cells MCF-10F, which are estrogen receptor alpha negative, with 17-beta estradiol (E(2)) or its metabolite 4-OH-estradiol (4-OH-E(2)), each one either alone or in combination with the antiestrogen ICI-182-780. Treated cells were maintained for several passages in culture and evaluated for colony formation in agar-methocel (CE), tri-dimensional growth in collagen matrix, invasiveness in matrigel, and cell cycle analysis by flow cytometry. Both E(2) and 4-HO-E(2), at all the doses tested, in the presence or absence of ICI-182-780, increased CE and decreased the cells' ductulogenic capacity. They also increased the invasiveness and the number of cells in the S phase of the cell cycle. Our data clearly demonstrate that E(2) and 4-OH-E(2) increase cell proliferation and induce transformation in MCF-10F cells, phenomena that are not abrogated by ICI-182-780. The failure of the antiestrogen to abrogate the transformation phenotypes led us to hypothesize that estrogen-induced transformation is occurring by a non-estrogen receptor alpha-mediated process, more probably through the genotoxic effect of the estrogen metabolite 4-HO-E(2).

    Topics: Agar; Breast; Cell Cycle; Cell Line; Cell Line, Tumor; Cell Proliferation; Collagen; Dose-Response Relationship, Drug; Drug Combinations; Epithelial Cells; Estradiol; Estrogen Receptor alpha; Estrogens; Estrogens, Catechol; Female; Flow Cytometry; Fulvestrant; G1 Phase; Humans; Laminin; Neoplasm Invasiveness; Phenotype; Proteoglycans; Resting Phase, Cell Cycle

2005
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