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|Title:||Circumvention of tamoxifen resistance by the pure anti-estrogen ICI 182,780.||Austin Authors:||Hu, X F;Veroni, M;De Luise, M;Wakeling, A;Sutherland, R;Watts, C K;Zalcberg, John R||Affiliation:||Department of Medicine, Heidelberg Repatriation Hospital, Victoria, Australia||Issue Date:||11-Nov-1993||Publication information:||International Journal of Cancer. Journal International Du Cancer; 55(5): 873-6||Abstract:||Both primary and acquired resistance to the growth-inhibitory effects of anti-estrogens (e.g., tamoxifen) limits the clinical usefulness of these drugs in the treatment of breast cancer. The new, steroidal anti-estrogen ICI 182,780 was tested for its ability to inhibit the proliferation of a tamoxifen-resistant variant of the parental MCF-7 human breast-cancer cell line. Two cell lines cloned from the MCF-7 line were used for these experiments: a tamoxifen-sensitive line, MCF 5-21, and a tamoxifen-resistant line, MCF 5-23. Compared with tamoxifen, ICI 182,780 appeared to be 150 and 1540 times more effective in inhibiting cell growth in the 5-21 and 5-23 sub-lines respectively. ICI 182,780 completely circumvented tamoxifen resistance at a concentration of (5 to 10) x 10(-9) M in this model. Based on IC50 concentrations, the 5-23 line was 22-fold more resistant to tamoxifen than the 5-21 line, but only 2-fold more resistant to ICI 182,780, reducing relative resistance by 10-fold in the resistant line. There were no differences in ER parameters between the 2 lines. ER numbers/cell were: 40500 and 34800 and the KD 0.48 and 0.15 x 10(-9) M in the 5-21 and 5-23 cells respectively. In the 5-23 cells, the concentrations of ICI 182,780 and tamoxifen resulting in a 50% inhibition of 3H-estradiol binding were 2.3 x 10(-8) M and 1 x 10(-6) M, respectively (cf. estradiol 0.89 x 10(-9) M). Thus, one potential mechanism for the increased effectiveness of ICI 182,780 may relate to the increased affinity of this drug for the estrogen receptor as compared with tamoxifen.||Gov't Doc #:||8244585||URI:||http://ahro.austin.org.au/austinjspui/handle/1/13291||URL:||https://pubmed.ncbi.nlm.nih.gov/8244585||Type:||Journal Article||Subjects:||Binding Sites
Cell Division.drug effects
Estradiol.analogs & derivatives.metabolism.pharmacology
Tumor Cells, Cultured
|Appears in Collections:||Journal articles|
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