The role of dietary polyphenols in alternating DNA methylation in cancer

被引:5
作者
Nanakali, Nadir Mustafa Qadir [1 ,2 ]
Dana, Parisa Maleki [3 ]
Sadoughi, Fatemeh [3 ]
Asemi, Zatollah [3 ]
Sharifi, Mehran [4 ]
Asemi, Reza [4 ]
Yousefi, Bahman [5 ,6 ]
机构
[1] Cihan Univ Erbil, Coll Sci, Dept Biomed Sci, Erbil, Kurdistan Regio, Iraq
[2] Salahaddin Univ Erbil, Coll Educ, Dept Biol, Erbil, Kurdistan Regio, Iraq
[3] Kashan Univ Med Sci, Res Ctr Biochem & Nutr Metab Dis, Inst Basic Sci, Kashan, Iran
[4] Isfahan Univ Med Sci, Seyyed Al Shohada Hosp, Canc Prevent Res Ctr, Sch Med,Dept Internal Med, Esfahan, Iran
[5] Tabriz Univ Med Sci, Mol Med Res Ctr, Tabriz, Iran
[6] Tabriz Univ Med Sci, Fac Med, Dept Biochem, Tabriz, Iran
关键词
Curcumin; DNA methylation; DNMT; EGCG; quercetin; resveratrol; GREEN TEA POLYPHENOL; GENE PROMOTER METHYLATION; TUMOR-SUPPRESSOR GENES; BREAST-CANCER; EPIGENETIC REACTIVATION; CAFFEIC ACID; RAR-BETA; CURCUMIN; CELLS; QUERCETIN;
D O I
10.1080/10408398.2022.2100313
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Natural products such as curcumin, quercetin, and resveratrol have been shown to have antitumor effectsand several studies have examined their role in treating cancer, either alone or in combination with other chemotherapeutic drugs. These compounds are capable of affecting different cancer-related mechanisms, such as proliferation, inflammation, invasion, and metastasis. Along with all of the benefits of these agents, affecting epigenetic processes is one of the most important aspects of their impact. Epigenetic modifications can be categorized into three main processes that include DNA methylation, histone modification, and regulation of small non-coding RNAs. Therefore, targeting DNA methylation can be used as a cancer treatment strategy by identifying or developing methylation modulators. Herein, we take a look into the studies investigating the role of natural products (e.g. curcumin, resveratrol, epigallocatechin gallate (EGCG), and quercetin) in alternating the DNA methylation status of various cancer cells. We discuss how these compounds reduce the expression of enzymes mediating the methylation of tumor suppressor genes and thereby, increasing the expression of tumor suppressors while reactivating antitumor signaling pathways.
引用
收藏
页码:12256 / 12269
页数:14
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