Down-regulation of p21 WAF1/CIP1 or p27 Kip1 abrogates antiestrogen-mediated cell cycle arrest in human breast cancer cells

• Published in: Proceedings of the National Academy of Sciences - PNAS 2000-08, Vol.97 (16), p.9042-9046
• Main Authors: Cariou, Sandrine, Donovan, Jeffrey C. H., Flanagan, W. M., Milic, Andrea, Bhattacharya, Nandita, Slingerland, Joyce M.
• Format: Article
• Language: English
• ISSN: 0027-8424; 1091-6490
• DOI: 10.1073/pnas.160016897

Estrogens and antiestrogens influence the G 1 phase of the cell cycle. In MCF-7 breast cancer cells, estrogen stimulated cell cycle progression through loss of the kinase inhibitor proteins (KIPs) p27 and p21 and through G 1 cyclin-dependent kinase (cdk) activation. Treatment with antiestrogen drugs, Tamoxifen or ICI 182780, caused cell cycle arrest, with up-regulation of both p21 and p27 levels, an increase in their binding to cyclin E–cdk2, and kinase inhibition. The requirement for these KIPs in the arrests induced by estradiol depletion or by antiestrogens was investigated with antisense. Antisense inhibition of p21 or p27 expression in estradiol-depleted or antiestrogenarrested MCF-7 led to abrogation of cell cycle arrest, with loss of cyclin E-associated KIPs, activation of cyclin E–cdk2, and S phase entrance. These data demonstrate that depletion of either p21 or p27 can mimic estrogen-stimulated cell cycle activation and indicate that both of these KIPs are critical mediators of the therapeutic effects of antiestrogens in breast cancer.