Wang Neng, Wang Zhiyu, Wang Yu, Xie Xiaoming, Shen Jiangang, Peng Cheng, You Jieshu, Peng Fu, Tang Hailin, Guan Xinyuan, Chen Jianping
School of Chinese Medicine, Li Ka Shing Faculty of Medicine, the University of Hong Kong, Hong Kong.
Department of Mammary Disease, Guangdong Provincial Hospital of Chinese Medicine, The Second Clinical Medical College, Guangzhou University of Chinese Medicine, Guangdong, China.
Oncotarget. 2015;6(12):9854-76. doi: 10.18632/oncotarget.3396.
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 β-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.
乳腺癌干细胞(CSCs)被认为是乳腺肿瘤发生的根源。先前的研究表明,异甘草素(ISL)有效地限制了乳腺癌干细胞的活性。然而,ISL的防癌活性及其精确的分子机制在很大程度上仍不清楚。在此,我们报道了ISL作为一种靶向WIF1的天然去甲基化剂预防乳腺癌的新功能。给予ISL可抑制体内乳腺癌的起始和进展,并伴有CSC样细胞群的减少。全基因组表达谱分析进一步确定WIF1是ISL治疗的主要反应基因,同时伴有乳腺癌干细胞中β-连环蛋白信号通路的下调和G0/G1期阻滞。此外,抑制WIF1可显著减轻ISL对CSC的限制作用,甲基化分析进一步表明,ISL通过促进WIF1启动子的去甲基化来增强其基因表达,这与抑制DNMT1甲基转移酶密切相关。分子对接分析最终表明,ISL可以稳定地对接至DNMT1的催化结构域。综上所述,我们的研究结果不仅提供了临床前证据来证明使用ISL作为膳食补充剂抑制乳腺癌发生,而且还为WIF1作为乳腺癌预防的表观遗传靶点提供了新的线索。