Dietary compound isoliquiritigenin prevents mammary carcinogenesis by inhibiting breast cancer stem cells through WIF1 demethylation

被引:62
|
作者
Wang, Neng [1 ]
Wang, Zhiyu [1 ,2 ]
Wang, Yu [3 ]
Xie, Xiaoming [4 ]
Shen, Jiangang [1 ]
Peng, Cheng [5 ]
You, Jieshu [1 ]
Peng, Fu [1 ]
Tang, Hailin
Guan, Xinyuan [6 ]
Chen, Jianping [1 ,5 ]
机构
[1] Univ Hong Kong, Sch Chinese Med, Li Ka Shing Fac Med, Hong Kong, Hong Kong, Peoples R China
[2] Guangzhou Univ Chinese Med, Dept Mammary Dis, Guangdong Prov Hosp Chinese Med, Clin Med Coll 2, Guangzhou, Guangdong, Peoples R China
[3] Univ Hong Kong, Dept Pharmacol, Li Ka Shing Fac Med, Hong Kong, Hong Kong, Peoples R China
[4] Sun Yat Sen Univ, Canc Ctr, Dept Breast Oncol,Collaborat Innovat Ctr Canc Med, State Key Lab Oncol South China, Guangzhou 510275, Guangdong, Peoples R China
[5] Chengdu Univ Tradit Chinese Med, Sch Pharmaceut Sci, Chengdu, Peoples R China
[6] Univ Hong Kong, Dept Clin Oncol, Li Ka Shing Fac Med, Hong Kong, Hong Kong, Peoples R China
关键词
mammary tumorigenesis; cancer stem cells; WIF1; demethylation; DNMT1; Isoliquiritigenin; FACTOR-I WIF1; DNA METHYLATION; PHASE-I; WNT; CHEMOPREVENTION; EXPRESSION; TUMORIGENESIS; 5-AZACYTIDINE; GROWTH; HYPERMETHYLATION;
D O I
10.18632/oncotarget.3396
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Breast cancer stem cells (CSCs) are considered as the root of mammary tumorigenesis. Previous studies have demonstrated that ISL efficiently limited the activities of breast CSCs. However, the cancer prevention activities of ISL and its precise molecular mechanisms remain largely unknown. Here, we report a novel function of ISL as a natural demethylation agent targeting WIF1 to prevent breast cancer. ISL administration suppressed in vivo breast cancer initiation and progression, accompanied by reduced CSC-like populations. A global gene expression profile assay further identified WIF1 as the main response gene of ISL treatment, accompanied by the simultaneous downregulation of beta-catenin signaling and G0/G1 phase arrest in breast CSCs. In addition, WIF1 inhibition significantly relieved the CSC-limiting effects of ISL and methylation analysis further revealed that ISL enhanced WIF1 gene expression via promoting the demethylation of its promoter, which was closely correlated with the inhibition of DNMT1 methyltransferase. Molecular docking analysis finally revealed that ISL could stably dock into the catalytic domain of DNMT1. Taken together, our findings not only provide preclinical evidence to demonstrate the use of ISL as a dietary supplement to inhibit mammary carcinogenesis but also shed novel light on WIF1 as an epigenetic target for breast cancer prevention.
引用
收藏
页码:9854 / 9876
页数:23
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