Tea flavan-3-ols as modulating factors in endoplasmic reticulum function |
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Authors: | Katalin Ré vé sz,Anna Tü tt?Pé ter Szelé nyi,Laura Konta |
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Affiliation: | Department of Medical Chemistry, Molecular Biology and Pathobiochemistry, Semmelweis University, Budapest, Hungary |
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Abstract: | Regular green tea consumption has been shown to reduce the risk of cancer and diabetes mellitus. These effects are attributed to tea flavan-3-ols, especially to epigallocatechin gallate; however, the molecular targets and mechanisms of action are still subject of extensive research. The special roles of the endoplasmic reticulum (ER) in biotransformation, protein synthesis, calcium homeostasis, and glucose production make this organelle a potential target of the antitumor and antidiabetic effects of tea flavan-3-ols. The purpose of this review is to present evidence for the biologic actions of tea flavan-3-ols on specific ER targets associated with normal function and disease. Reactivation of chemical carcinogens can be reduced by tea flavan-3-ols through inhibition of glucuronide transport across the ER membrane. Catechins modulate Ca2+ release from the ER lumen and interfere with glycoprotein maturation, which can lead to decreased viability and increased drug sensitivity of tumor cells. Epigallocatechin gallate inhibits glucose transport across the ER membrane, which can underlie the reduction of hepatic glucose production by tea flavan-3-ols. These mechanisms likely contribute to the chemopreventive and glucose-lowering effects of tea catechins. Investigating the effects of flavan-3-ols on ER functions is a promising field of medical and biochemical research to understand disease and improve health. |
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Keywords: | ATPase, adenosine triphosphatase BiP, immunoglobulin heavy chain binding protein ECG, epicatechin gallate EGCG, epigallocatechin gallate ER, endoplasmic reticulum ERAD, ER-associated degradation G6P, glucose-6-phosphate G6Pase, glucose-6-phosphatase G6PT, G6P translocase PLC, phospholipase C RyR, ryanodine receptor SERCA, sarco/endoplasmic reticulum calcium ATPase UGT, UDP-glucuronosyltransferase UPR, unfolded protein response. |
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