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pubmed-article:12168814pubmed:abstractTextSelective estrogen receptor modifiers (SERMs) are used chronically in the treatment of breast cancer and osteoporosis but some patients become resistant, at which point second-line SERMs are considered as options. Because the use of SERMs is increasing and breast cancer is so common, we tested the hypothesis that treatment with SERMs can induce cross-resistance to other SERMs. We used three cultured breast carcinoma cell lines (MCF-7, ZR-75-1, and T47D) which are estrogen-receptor-positive (ER+) and are prone to developing resistance to hormonal treatment. Cell lines were exposed to increasing doses of raloxifene. Raloxifene-resistant clones were selected and tested for cross-resistance to tamoxifen. Compared to untreated cells, raloxifene-resistant clones showed an increased IC50 (reduced potency) of about 15,000-fold with no apparent change in maximal inhibition of cell growth. These same raloxifene-resistant clones were also about 15-fold more resistant to the growth-inhibiting effects of tamoxifen. While the resistance to tamoxifen is considerably less marked (1000-fold less), it is large enough to raise the question as to whether patients who become resistant to raloxifene will benefit by switching to tamoxifen or vice versa.lld:pubmed
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pubmed-article:12168814pubmed:authorpubmed-author:BomanB MBMlld:pubmed
pubmed-article:12168814pubmed:authorpubmed-author:FanY SYSlld:pubmed
pubmed-article:12168814pubmed:authorpubmed-author:FieldsJ ZJZlld:pubmed
pubmed-article:12168814pubmed:authorpubmed-author:TamE WEWlld:pubmed
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pubmed-article:12168814pubmed:pagination1379-83lld:pubmed
pubmed-article:12168814pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:12168814pubmed:articleTitleDevelopment of cross-resistance to tamoxifen in raloxifene-treated breast carcinoma cells.lld:pubmed
pubmed-article:12168814pubmed:affiliationDivision of Genetic and Preventive Medicine, Thomas Jefferson University, Philadelphia, PA 19107, USA.lld:pubmed
pubmed-article:12168814pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:12168814pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed