Discovering alkylamide derivatives of bexarotene as new therapeutic agents against triple-negative breast cancer

被引:8
作者
Chen, Luxi [1 ]
Long, Chao [1 ]
Nguyen, Jennifer [1 ]
Kumar, Dhiraj [1 ]
Lee, Jiyong [1 ]
机构
[1] Univ Texas Dallas, Dept Chem & Biochem, 800 W Campbell Rd, Richardson, TX 75080 USA
关键词
Triple-negative breast cancer; Apoptosis; Cancer stem cell; Epithelial-mesenchymal transition; Anti-cancer therapeutics; STEM-CELLS; PHENOTYPE; CARCINOMA; PATTERNS; SUBTYPES;
D O I
10.1016/j.bmcl.2017.12.033
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Triple-negative breast cancer (TNBC) has been reported to be correlated with high expression of proliferation markers as well as constitutive activation of metastasis-relevant signaling pathways. For many years, breast cancer researchers have been investigating specific and effective methods to treat or to control the development of TNBC, but promising therapeutic options remain elusive. In this study, we have demonstrated that alkylamide derivatives of bexarotene DK-1-150 and DK-1-166 induce apoptotic cell death in TNBC cell lines without causing cytotoxicity in the normal mammary epithelial cell line. Furthermore, the bexarotene derivatives also showed significant effects in inhibiting TNBC cell proliferation and migration, modulating cancer stem cell markers expressions, as well as limiting the epithelial-mesenchymal transition (EMT) activities of TNBC cell lines in terms of downregulating EMT marker and blocking nuclear translocation of beta-catenin. Therefore, we propose the alkylamide derivatives of bexarotene as potential candidates for novel anticancer therapeutics against TNBC. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:420 / 424
页数:5
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