Identification of BCAR3 by a random search for genes involved in antiestrogen resistance of human breast cancer cells.
1998-05-15
Article
| Related Files |
|---|
|
Redirect to publisher's version
(publisher's version.url.txt, 42 bytes) |
The antiestrogen tamoxifen is important in the treatment of hormone-dependent breast cancer, although development of resistance is inevitable. To unravel the molecular mechanisms of antiestrogen resistance, a search for involved genes was initiated. Retrovirus-mediated insertional mutagenesis was applied to human ZR-75-1 breast cancer cells. Infected cells were subjected to tamoxifen selection and a panel of resistant cell clones was established. Screening for a common integration site resulted in the identification of a novel gene designated BCAR3. Transfer of this locus by cell fusion or transfection of the BCAR3 cDNA to ZR75-1 and MCF-7 cells induces antiestrogen resistance. BCAR3 represents a putative SH2 domain-containing protein and is partly homologous to the cell division cycle protein CDC48.
- Animals
- Female
- Humans
- Amino Acid Sequence
- Cloning, Molecular
- Molecular Sequence Data
- Base Sequence
- Tumor Cells, Cultured
- Gene Expression
- Binding Sites
- Sequence Homology, Amino Acid
- Drug Resistance, Neoplasm/genetics
- Transcription, Genetic
- RNA, Messenger
- DNA, Complementary
- Cell Fusion
- Antineoplastic Agents, Hormonal/*pharmacology
- Estrogen Antagonists/*pharmacology
- Tamoxifen/*pharmacology
- Protein Biosynthesis
- Breast Neoplasms/drug therapy/*genetics
- DNA, Neoplasm
- Receptors, Cyclic AMP/*genetics