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Human breast cancer cell lines resistant to pure anti-estrogens are sensitive to tamoxifen treatment

✍ Scribed by Anne E. Lykkesfeldt; Søren S. Larsen; Per Briand


Publisher
John Wiley and Sons
Year
1995
Tongue
French
Weight
760 KB
Volume
61
Category
Article
ISSN
0020-7136

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✦ Synopsis


Abstract

The pure steroidal anti‐estrogens ICI 164,384 and ICI 182,780 are very potent growth inhibitors of the estrogen receptor‐positive human breast cancer cell line MCF‐7. However, long‐term treatment of MCF‐7 cells with 10^−7^ M concentrations of these compounds results in selection of proliferating colonies of resistant cells. Our report describes 4 ICI 164,384‐ and 3 ICI 182,780‐resistant MCF‐7 sublines established after long‐term treatment. Resistant sublines are estrogen receptor‐positive, and all sublines have lost expression and estrogen inducibility of the progesterone receptor protein. Based on IC~50~ concentrations, all tested resistant sublines had a reduced sensitivity to pure anti‐estrogens on the order of 100‐ to 1000‐fold compared with parent MCF‐7 cells. All resistant cell lines have survived propagation for more than 15 subcultivations in the presence of 10^−7^ M pure anti‐estrogen. The MCF‐7/182^R^‐6 subline has been tested for stability of resistance and appeared to be stably resistant after 13 weeks of propagation without the selective pressure of ICI 182,780. Cell lines resistant to the ICI 182,780 compound are cross‐resistant to the ICI 164,384 compound and vice versa. However, the sublines resistant to pure anti‐estrogens are sensitive to tamoxifen. Our results show that although the pure steroidal anti‐estrogens are very potent growth inhibitors, they do not circumvent development of resistance. © 1995 Wiley‐Liss, Inc.


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Resistance of human breast-cancer cells
✍ Søren S. Larsen; Mogens W. Madsen; Bettina L. Jensen; Anne E. Lykkesfeldt 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 French ⚖ 145 KB 👁 3 views

To elucidate the mechanisms responsible for the development of anti-estrogen resistance, we have cloned and established 3 stable ICI-182,780-resistant sub-lines, MCF-7/182 R -1, MCF-7/182 R -6 and MCF-7/182 R -7 from the estrogen-receptor(ER)-positive and estrogen-responsive human breastcancer MCF-7