Effects of Different Forms of Anthocyanins on the Growth Inhibition and Gene Expression of Colorectal Cancer Cells
文献类型: 外文期刊
作者: Liu, Weidong 1 ; Feng, Siting 1 ; He, Dou 1 ; Liu, Pei 1 ; Guo, Jian 1 ; Chen, Xinyu 1 ; Hu, Chenghao 1 ; Gao, Fei 1 ; Ren, Shuqiang 1 ;
作者机构: 1.Chinese Acad Agr Sci, Minist Agr & Rural Affairs, Agr Genom Inst Shenzhen, Genome Anal Lab, Shenzhen 518000, Peoples R China
2.Henan Univ, Dept Life Sci, Kaifeng 475004, Peoples R China
3.Shenzhen Res Fac Henan Univ, Shenzhen 518000, Peoples R China
4.Qingdao Agr Univ, Dept Life Sci, Qingdao 266109, Peoples R China
5.Shanxi Agr Univ, Coll Agron, Jinzhong 030801, Peoples R China
6.Guangxi Univ, Coll Anim Sci & Technol, Nanning 530004, Peoples R China
7.Univ Copenhagen, Fac Hlth & Med Sci, Dept Vet & Anim Sci, Comparat Pediat & Nutr, Copenhagen, Denmark
关键词: anthocyanins; antiproliferation; colorectal cancer; drug repurposing
期刊名称:JOURNAL OF FOOD BIOCHEMISTRY ( 影响因子:4.2; 五年影响因子:4.3 )
ISSN: 0145-8884
年卷期: 2024 年 2024 卷 1 期
页码:
收录情况: SCI
摘要: Scope: Anthocyanins obtained from the diet have therapeutic potential for various cancers, including colorectal cancer (CRC). Given the diverse forms of anthocyanins, it is unclear whether different types of anthocyanins share common pathways in regulating intestinal cell function. This study aims to explore the core gene pathways modulated by anthocyanins in intestinal cells and to identify potential compounds with similar therapeutic effects.Methods and Results: Three different forms of anthocyanins (cyanidin chloride, cyanidin 3-O-glucoside, and cyanidin 3-O-rutinoside) were used to treat CRC cells at different concentrations and time points, and growth inhibition was observed for all anthocyanins, with varying patterns. RNA-seq analysis showed that the regulatory pathways of anthocyanins with different structures were different, and the time factor had a greater effect. Time-series analysis of regulatory genes shared among different concentrations and structures of anthocyanins was performed. By overlapping with a public PPAR target gene set, a core gene set across three types of anthocyanins was identified and used in Connectivity Map (CMap) analysis to screen for compounds. The repositioned drug candidates included known anticancer drugs that have effects of transcriptome interventions like anthocyanins.Conclusion: These findings provide new insights into the mechanisms that underlie the anti-CRC effects of anthocyanins and may facilitate the development of novel therapeutic agents for CRC.
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