Green tea and its anti-angiogenesis effects

(2017) Green tea and its anti-angiogenesis effects. Biomedicine & Pharmacotherapy. pp. 949-956. ISSN 0753-3322

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Abstract

The development of new blood vessels from a pre-existing vasculature (also known as angiogenesis) is required for many physiological processes including embryogenesis and post-natal growth. However, pathological angiogenesis is also a hallmark of cancer and many ischaemic and inflammatory diseases. The pro-angiogenic members of the VEGF family (vascular endothelial growth factor family), VEGF-A, VEGF-B, VEGF-C, VEGF-D and placental growth factor (PlGF), and the related receptors, VEGFR-1, VEGFR2 and VEGFR-3 have a central and decisive role in angiogenesis. Indeed, they are the targets for anti-angiogenic drugs currently approved. Green tea (from the Camellia sinensis plant) is one of the most popular beverages in the world. It is able to inhibit angiogenesis by different mechanisms such as microRNAs (miRNAs). Green tea and its polyphenolic substances (like catechins) show chemo-preventive and chemotherapeutic features in various types of cancer and experimental models for human cancers. The tea catechins, including (-)-epigallocatechin-3-gallate (EGCG), have multiple effects on the cellular proteome and signalome. Note that the polyphenolic compounds from green tea are able to change the miRNA expression profile associated with angiogenesis in various cancer types. This review focuses on the ability of the green tea constituents to suppress angiogenesis signaling and it summarizes the mechanisms by which EGCG might inhibit the VEGF family. We also highlighted the miRNAs affected by green tea which are involved in anti-angiogenesis. (c) 2017 Elsevier Masson SAS. All rights reserved.

Item Type: Article
Keywords: angiogenesis vegf green tea epigallocatechin-3-gallate microrna endothelial growth-factor receptor tyrosine kinases hepatocellular-carcinoma cells breast-cancer cells nf-kappa-b circulating micrornas vascular development in-vivo diagnostic biomarker signaling pathway
Divisions: Other
Page Range: pp. 949-956
Journal or Publication Title: Biomedicine & Pharmacotherapy
Journal Index: ISI
Volume: 89
Identification Number: https://doi.org/10.1016/j.biopha.2017.01.161
ISSN: 0753-3322
Depositing User: مهندس مهدی شریفی
URI: http://eprints.mui.ac.ir/id/eprint/599

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