Phosphatidylinositol-3 Kinase Inhibitors, Buparlisib and Alpelisib, Sensitize Estrogen Receptor-positive Breast Cancer Cells to Tamoxifen

• Published in: Scientific reports 2017-08, Vol.7 (1), p.9842-10, Article 9842
• Main Authors: Chen, I-Chun, Hsiao, Li-Ping, Huang, I-Wen, Yu, Huei-Chieh, Yeh, Ling-Chun, Lin, Ching-Hung, Wei-Wu Chen, Tom, Cheng, Ann-Lii, Lu, Yen-Shen
• Format: Article
• Language: English
• Subjects: 1-Phosphatidylinositol 3-kinase; 13/1; 13/106; 13/2; 13/51; 631/67/1347; 64/60; 692/4028/67/1059/602; AKT protein; AKT1 protein; Aminopyridines - pharmacology; Antineoplastic Agents, Hormonal - pharmacology; Apoptosis - drug effects; Breast cancer; Cell Line, Tumor; Clinical trials; Drug Resistance, Neoplasm - drug effects; Drug Synergism; Estrogen Receptor alpha - genetics; Estrogen Receptor alpha - metabolism; Estrogen receptors; Estrogens; Female; Humanities and Social Sciences; Humans; Immunoblotting; Metastases; Morpholines - pharmacology; multidisciplinary; Mutation; Phosphatidylinositol 3-Kinases - antagonists & inhibitors; Phosphatidylinositol 3-Kinases - metabolism; Phosphorylation; Proto-Oncogene Proteins c-akt - metabolism; Receptors, Estrogen - genetics; Receptors, Estrogen - metabolism; Science; Science (multidisciplinary); Signal Transduction - drug effects; Tamoxifen; Tamoxifen - pharmacology; Thiazoles - pharmacology
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-017-10555-z

Tamoxifen is the standard first-line hormonal therapy for premenopausal women with estrogen receptor (ER)-positive metastatic breast cancer (BC). One of the crucial mechanisms underlying hormonal therapy resistance is the collateral activation of the phosphatidylinositol-3 kinase (PI3K)/AKT pathway. We explored whether PI3K inhibitors, buparlisib and alpelisib, enhance the efficacy of tamoxifen against ER-positive BC cells. We have observed a s ynergism between alpelisib or buparlisib and tamoxifen in the treatment for ER-positive BC cell lines harboring different PI3K alterations. Immunoblotting analysis showed alpelisib, buparlisib, or either drug in combination with tamoxifen downregulated the PI3K downstream targets in the MCF-7 and ZR75-1 cells. In the MCF-7 cells transfected with a constitutive active (myristoylated) AKT1 construct or mutant ER, the synergistic effect between alpelisib and tamoxifen was markedly attenuated, indicating that synergism depends on AKT inhibition or normally functioning ER. Combining alpelisib or buparlisib with tamoxifen also attenuated MCF-7 tumor growth in Balb/c nude mice. Our data suggest that additional PI3K blockade might be effective in enhancing the therapeutic effect of tamoxifen in ER-positive BC and support the rationale combination in clinical trials.