Functional identification of genes causing estrogen independence of human breast cancer cells
Breast Cancer Research and Treatment , Volume 114 - Issue 1 p. 23- 30
Endocrine treatment of breast cancer is widely applied and effective. However, in advanced disease cases, the tumors will eventually progress into an estrogen-independent and therapy-resistant phenotype. To elucidate the molecular mechanisms underlying this endocrine therapy failure, we applied retroviral insertion mutagenesis to identify the main genes conferring estrogen independence to human breast cancer cells. Estrogen-dependent ZR-75-1 cells were infected with replication-defective retroviruses followed by selection with the anti-estrogen 4-hydroxy-tamoxifen. In the resulting panel of 79 tamoxifen-resistant cell lines, the viral integrations were mapped within the human genome. Genes located in the immediate proximity of the retroviral integration sites were characterized for altered expression and their capacity to confer anti-estrogen resistance when transfected into breast cancer cells. Out of 15 candidate BCAR (breast cancer anti-estrogen resistance) genes, seven (AKT1, AKT2, BCAR1, BCAR3, EGFR, GRB7, and TRERF1/BCAR2) were shown to directly underlie estrogen independence. Our results show that insertion mutagenesis is a powerful tool to identify BCAR loci, which may provide insights into the molecular and cellular mechanisms of breast tumor progression and therapy resistance thereby offering novel targets for the development of tailor-made therapeutical and prevention strategies.
|Cell proliferation control, Endocrine therapy, Functional screen, Genetic screen, Insertion mutagenesis, Tamoxifen resistance|
|Breast Cancer Research and Treatment|
|Organisation||Erasmus MC: University Medical Center Rotterdam|
van Agthoven, A.J, Veldscholte, J, Smid, M, Vreede, L, Broertjes, M, de Vries, I, … Dorssers, L.C.J. (2009). Functional identification of genes causing estrogen independence of human breast cancer cells. Breast Cancer Research and Treatment, 114(1), 23–30. doi:10.1007/s10549-008-9969-5