The Potential Role of Epigallocatechin-3-Gallate (EGCG) in Breast Cancer Treatment

被引:19
|
作者
Marin, Victor [1 ]
Burgos, Viviana [2 ,3 ]
Perez, Rebeca [1 ]
Maria, Durvanei Augusto [4 ]
Pardi, Paulo [5 ]
Paz, Cristian [1 ]
机构
[1] Univ La Frontera, Ctr CEBIM, Fac Med, Dept Basic Sci,Lab Nat Prod & Drug Discovery, Temuco 4780000, Chile
[2] Univ Catolica Temuco, Fac Recursos Nat, Dept Ciencias Biol & Quim, Rudecindo Ortega, Temuco, Chile
[3] Univ Santo Tomas, Fac Ciencias, Dept Ciencias Bas, Temuco 4780000, Chile
[4] Butantan Inst, Dev & Innovat Lab, Sao Paulo, Brazil
[5] ENIAC Univ Ctr, Nucleo Pesquisas NUPE, BR-07012030 Guarulhos, Brazil
关键词
epigallocatechin-3-gallate; breast cancer; synergistic chemotherapy; metabolism; drug delivery; GREEN TEA POLYPHENOL; DOWN-REGULATION; (-)-EPIGALLOCATECHIN GALLATE; SIGNALING PATHWAYS; IMMUNE SUPPRESSION; GROWTH-INHIBITION; DELIVERY-SYSTEM; CELLS; PREVENTION; MDA-MB-231;
D O I
10.3390/ijms241310737
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Breast cancer is one of the most diagnosed cancers worldwide, with an incidence of 47.8%. Its treatment includes surgery, radiotherapy, chemotherapy, and antibodies giving a mortality of 13.6%. Breast tumor development is driven by a variety of signaling pathways with high heterogeneity of surface receptors, which makes treatment difficult. Epigallocatechin-3-gallate (EGCG) is a natural polyphenol isolated as the main component in green tea; it has shown multiple beneficial effects in breast cancer, controlling proliferation, invasion, apoptosis, inflammation, and demethylation of DNA. These properties were proved in vitro and in vivo together with synergistic effects in combination with traditional chemotherapy, increasing the effectiveness of the treatment. This review focuses on the effects of EGCG on the functional capabilities acquired by breast tumor cells during its multistep development, the molecular and signal pathways involved, the synergistic effects in combination with current drugs, and how nanomaterials can improve its bioavailability on breast cancer treatment.
引用
收藏
页数:13
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