Targeting Aberrant p70S6K Activation for Estrogen Receptor-Negative Breast Cancer Prevention.
Targeting Aberrant p70S6K Activation for Estrogen Receptor-Negative Breast Cancer Prevention.
复制标题
针对雌激素受体阴性乳腺癌预防的异常 p70S6K 激活。
DOI：
10.1158/1940-6207.capr-17-0106
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发表时间：
2017
期刊：
影响因子：
--
通讯作者：
Yu,Dihua
中科院分区：
文献类型：
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作者：
Wang,Xiao;Yao,Jun;Wang,Jinyang;Zhang,Qingling;Brady,SamuelW;Arun,Banu;Seewaldt,VictoriaL;Yu,Dihua
The prevention of estrogen receptor–negative (ER−) breast cancer remains a major challenge in the cancer prevention field, although antiestrogen and aromatase inhibitors have shown adequate efficacy in preventing estrogen receptor–positive (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 70 kDa ribosomal protein S6 kinase (p70S6K) signaling pathway was highly activated in ER−premalignant breast lesions and ER−breast cancer. In addition, p70S6K activation induced transformation of ER−human mammary epithelial cells (hMEC). Therefore, we explored the potential of targeting Akt/p70S6K in the p70S6K activated, ER−hMEC 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–G1phase, while it did not significantly reverse the abnormal acinar morphology of these hMECs. In addition, a brief treatment of LY2780301 in MMTV-neumice that developed atypical hyperplasia (ADH) and mammary intraepithelial neoplasia (MIN) 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 modelsin vitroand in the MMTV-neutransgenic mouse modelin vivoeffectively inhibited Akt/S6K signaling and reduced proliferation of hMECsin vitroand ADH/MIN lesionsin vivo, indicating its potential in prevention of p70S6K activated ER−breast cancer.Cancer Prev Res; 10(11); 641–50. ©2017 AACR.
