Abstract
In this study, T47D cell lines resistant to the antiestrogen fulvestrant were established and analyzed to explore, whether a switch to HER signaling, as seen in fulvestrant resistant MCF-7 cell lines, is a general resistance mechanism. We find that parental T47D cells depend on ER and HER signaling for growth. Fulvestrant resistant T47D cells have lost ER expression and, although HER2 was over expressed, growth was only partially driven by HER receptors. Instead c-Src was important for resistant growth. Thus, the T47D and MCF-7 model system unravel different resistance mechanisms which may be important for fulvestrant resistant breast cancer patients.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Blotting, Western
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Breast Neoplasms / metabolism*
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CSK Tyrosine-Protein Kinase
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Cell Line, Tumor
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Drug Resistance, Neoplasm / physiology*
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Estradiol / analogs & derivatives
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Estradiol / pharmacology
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Estrogen Antagonists / pharmacology
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Fulvestrant
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Humans
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Immunoprecipitation
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RNA, Small Interfering
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Real-Time Polymerase Chain Reaction
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Receptor, ErbB-2 / metabolism*
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Receptors, Estrogen / metabolism*
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Reverse Transcriptase Polymerase Chain Reaction
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Signal Transduction / physiology*
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src-Family Kinases / metabolism*
Substances
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Estrogen Antagonists
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RNA, Small Interfering
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Receptors, Estrogen
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Fulvestrant
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Estradiol
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ERBB2 protein, human
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Receptor, ErbB-2
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CSK Tyrosine-Protein Kinase
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src-Family Kinases
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CSK protein, human