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

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 r...

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Autores principales: Wang, Neng, Wang, Zhiyu, Wang, Yu, Xie, Xiaoming, Shen, Jiangang, Peng, Cheng, You, Jieshu, Peng, Fu, Tang, Hailin, Guan, Xinyuan, Chen, Jianping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4496402/
https://www.ncbi.nlm.nih.gov/pubmed/25918249
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author Wang, Neng
Wang, Zhiyu
Wang, Yu
Xie, Xiaoming
Shen, Jiangang
Peng, Cheng
You, Jieshu
Peng, Fu
Tang, Hailin
Guan, Xinyuan
Chen, Jianping
author_facet Wang, Neng
Wang, Zhiyu
Wang, Yu
Xie, Xiaoming
Shen, Jiangang
Peng, Cheng
You, Jieshu
Peng, Fu
Tang, Hailin
Guan, Xinyuan
Chen, Jianping
author_sort Wang, Neng
collection PubMed
description 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.
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spelling pubmed-44964022015-07-15 Dietary compound isoliquiritigenin prevents mammary carcinogenesis by inhibiting breast cancer stem cells through WIF1 demethylation Wang, Neng Wang, Zhiyu Wang, Yu Xie, Xiaoming Shen, Jiangang Peng, Cheng You, Jieshu Peng, Fu Tang, Hailin Guan, Xinyuan Chen, Jianping Oncotarget Research Paper 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. Impact Journals LLC 2015-03-26 /pmc/articles/PMC4496402/ /pubmed/25918249 Text en Copyright: © 2015 Wang et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Wang, Neng
Wang, Zhiyu
Wang, Yu
Xie, Xiaoming
Shen, Jiangang
Peng, Cheng
You, Jieshu
Peng, Fu
Tang, Hailin
Guan, Xinyuan
Chen, Jianping
Dietary compound isoliquiritigenin prevents mammary carcinogenesis by inhibiting breast cancer stem cells through WIF1 demethylation
title Dietary compound isoliquiritigenin prevents mammary carcinogenesis by inhibiting breast cancer stem cells through WIF1 demethylation
title_full Dietary compound isoliquiritigenin prevents mammary carcinogenesis by inhibiting breast cancer stem cells through WIF1 demethylation
title_fullStr Dietary compound isoliquiritigenin prevents mammary carcinogenesis by inhibiting breast cancer stem cells through WIF1 demethylation
title_full_unstemmed Dietary compound isoliquiritigenin prevents mammary carcinogenesis by inhibiting breast cancer stem cells through WIF1 demethylation
title_short Dietary compound isoliquiritigenin prevents mammary carcinogenesis by inhibiting breast cancer stem cells through WIF1 demethylation
title_sort dietary compound isoliquiritigenin prevents mammary carcinogenesis by inhibiting breast cancer stem cells through wif1 demethylation
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4496402/
https://www.ncbi.nlm.nih.gov/pubmed/25918249
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