Targeting Aberrant p70S6K Activation for Estrogen Receptor Negative Breast Cancer Prevention
Menée in vitro et à l'aide d'un modèle murin transgénique, cette étude met en évidence l'intérêt de cibler l'activation de la kinase p70S6K dans les lésions mammaires pré-cancéreuses n'exprimant pas les récepteurs des estrogènes pour prévenir le développement d'une tumeur maligne ER-
Résumé en anglais
The prevention of ER- breast cancer remains a major challenge in the cancer prevention field although anti-estrogen and aromatase inhibitors have shown adequate efficacy in preventing ER+ breast cancer. Lack of commonly expressed, druggable targets is a major obstacle for meeting this challenge. Previously, we detected the activation of Akt signaling pathway in atypical hyperplasic early stage lesions of patients. In the current study, we found that Akt and the downstream p70S6K signaling pathway was highly activated in ER- pre-malignant breast lesions and ER- breast cancer. Additionally, p70S6K activation induced transformation of ER- human mammary epithelial cells. Therefore, we explored the potential of targeting Akt/p70S6K in the p70S6K activated, ER- hMECs models and mouse mammary tumor models for the prevention of ER- breast cancer. We found that a clinically applicable Akt/p70S6K dual inhibitor, LY2780301, drastically decreased proliferation of hMECs with ErbB2-induced p70S6K activation via Cyclin B1 inhibition and cell cycle blockade at G0-G1 phase, while it did not significantly reverse the abnormal acinar morphology of these hMECs. In addition, a brief treatment of LY2780301 in MMTV-neu mice that developed atypia/ADH and mammary intraepithelial neoplasia lesions with activated p70S6K was sufficient to suppress S6 phosphorylation and decrease cell proliferation in hyperplasic MECs. In summary, targeting the aberrant Akt/p70S6K activation in ER- hMEC models in vitro and in the MMTV-neu transgenic mouse model in vivo effectively inhibited Akt/S6K signaling and reduced proliferation of hMECs in vitro and ADH/MIN lesions in vivo, indicating its potential in prevention of p70S6K activated ER- breast cancer.
