| Literature DB >> 27302166 |
Qianhui Dou1, Hai-Ning Chen2, Kui Wang3, Kefei Yuan1, Yunlong Lei4, Kai Li1, Jiang Lan3, Yan Chen1, Zhao Huang1, Na Xie1, Lu Zhang1, Rong Xiang5, Edouard C Nice6, Yuquan Wei1, Canhua Huang7.
Abstract
Breast cancer is the most common cancer among women worldwide, yet successful treatment remains a clinical challenge. Ivermectin, a broad-spectrum antiparasitic drug, has recently been characterized as a potential anticancer agent due to observed antitumor effects. However, the molecular mechanisms involved remain poorly understood. Here, we report a role for ivermectin in breast cancer suppression by activating cytostatic autophagy both in vitro and in vivo Mechanistically, ivermectin-induced autophagy in breast cancer cells is associated with decreased P21-activated kinase 1 (PAK1) expression via the ubiquitination-mediated degradation pathway. The inhibition of PAK1 decreases the phosphorylation level of Akt, resulting in the blockade of the Akt/mTOR signaling pathway. In breast cancer xenografts, the ivermectin-induced cytostatic autophagy leads to suppression of tumor growth. Together, our results provide a molecular basis for the use of ivermectin to inhibit the proliferation of breast cancer cells and indicate that ivermectin is a potential option for the treatment of breast cancer. Cancer Res; 76(15); 4457-69. ©2016 AACR. ©2016 American Association for Cancer Research.Entities:
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Year: 2016 PMID: 27302166 DOI: 10.1158/0008-5472.CAN-15-2887
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701