Estrogen receptor messenger RNA splice variants are not involved in antiestrogen resistance in sublines of MCF-7 human breast cancer cells.

• Abstract: Development of resistance to tamoxifen is a serious problem in treatment of breast cancer patients. Although the mechanisms for development of resistance are unclear, an altered expression of alternatively spliced estrogen receptor (ER) mRNA has been suggested to be involved. We have looked for differential expression of ER splice variants lacking exon 2 (ERdeltaE2), exon 3 (ERdeltaE3), exon 4 (ERdeltaE4), exon 5 (ERdeltaE5), exon 7 (ERdeltaE7), and exons 4 and 7 (ERdeltaE4, 7) in the human breast cancer cell line MCF-7 and 10 ER-positive MCF-7 sublines resistant to the antiestrogens tamoxifen, ICI 164,384 or ICI 182,780. No major differences in the expression were demonstrated between MCF-7 cells and resistant cells, indicating that ER splice variants are not involved in antiestrogen resistance in this model system. Furthermore, despite a high mRNA level of some of the ER splice variants, no corresponding proteins could be detected using Western blot analysis.
• Authors: M W Madsen, B E Reiter, S S Larsen, P Briand, A E Lykkesfeldt (Affiliation: Department of Tumor Endocrinology, Danish Cancer Society, Copenhagen, Denmark.)
• Journal: Cancer research (Cancer Res) Vol. 57 Issue 4 Pg. 585-9 (Feb 15 1997) ISSN: 0008-5472 [Print] UNITED STATES
• PMID: 9044830 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Antineoplastic Agents, Hormonal
• Estrogen Antagonists
• Polyunsaturated Alkamides
• RNA, Messenger
• RNA, Neoplasm
• Receptors, Estrogen
• Tamoxifen
• fulvestrant
• Estradiol
• ICI 164384

Topics

• Antineoplastic Agents, Hormonal (pharmacology)
• Breast Neoplasms (chemistry, genetics)
• Drug Resistance, Neoplasm (genetics)
• Estradiol (analogs & derivatives, pharmacology)
• Estrogen Antagonists (pharmacology)
• Female
• Genetic Vectors
• Humans
• Polyunsaturated Alkamides
• RNA Splicing (genetics)
• RNA, Messenger (metabolism)
• RNA, Neoplasm (metabolism)
• Receptors, Estrogen (analysis, genetics)
• Tamoxifen (pharmacology)
• Transfection
• Tumor Cells, Cultured (chemistry)