Cargando…
Epigallocatechin gallate (EGCG) suppresses epithelial-Mesenchymal transition (EMT) and invasion in anaplastic thyroid carcinoma cells through blocking of TGF-β1/Smad signaling pathways
Transforming growth factor (TGF)-β1 plays a crucial role in the epithelial-to-mesenchymal transition (EMT) in many cancer types and in thyroid cancers. Epigallocatechin-3-gallate (EGCG), the most important ingredient in the green tea, has been reported to possess antioxidant and anticancer activitie...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6650192/ https://www.ncbi.nlm.nih.gov/pubmed/31311401 http://dx.doi.org/10.1080/21655979.2019.1632669 |
_version_ | 1783438106903445504 |
---|---|
author | Li, Tingting Zhao, Ning Lu, Jie Zhu, Qingli Liu, Xinfeng Hao, Fengyun Jiao, Xuelong |
author_facet | Li, Tingting Zhao, Ning Lu, Jie Zhu, Qingli Liu, Xinfeng Hao, Fengyun Jiao, Xuelong |
author_sort | Li, Tingting |
collection | PubMed |
description | Transforming growth factor (TGF)-β1 plays a crucial role in the epithelial-to-mesenchymal transition (EMT) in many cancer types and in thyroid cancers. Epigallocatechin-3-gallate (EGCG), the most important ingredient in the green tea, has been reported to possess antioxidant and anticancer activities. However, the cellular and molecular mechanisms explaining its action have not been completely understood. In this study, we found that EGCG significantly suppresses EMT, invasion and migration in anaplastic thyroid carcinoma (ATC) 8505C cells in vitro by regulating the TGF-β/Smad signaling pathways. EGCG significantly inhibited TGF-β1-induced expression of EMT markers (E-cadherin reduction and vimentin induction) in 8505C cells in vitro. Treatment with EGCG completely blocked the phosphorylation of Smad2/3, translocation of Smad4. Taken together, these results suggest that EGCG suppresses EMT and invasion and migration by blocking TGFβ/Smad signaling pathways. |
format | Online Article Text |
id | pubmed-6650192 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-66501922020-07-16 Epigallocatechin gallate (EGCG) suppresses epithelial-Mesenchymal transition (EMT) and invasion in anaplastic thyroid carcinoma cells through blocking of TGF-β1/Smad signaling pathways Li, Tingting Zhao, Ning Lu, Jie Zhu, Qingli Liu, Xinfeng Hao, Fengyun Jiao, Xuelong Bioengineered Research Paper Transforming growth factor (TGF)-β1 plays a crucial role in the epithelial-to-mesenchymal transition (EMT) in many cancer types and in thyroid cancers. Epigallocatechin-3-gallate (EGCG), the most important ingredient in the green tea, has been reported to possess antioxidant and anticancer activities. However, the cellular and molecular mechanisms explaining its action have not been completely understood. In this study, we found that EGCG significantly suppresses EMT, invasion and migration in anaplastic thyroid carcinoma (ATC) 8505C cells in vitro by regulating the TGF-β/Smad signaling pathways. EGCG significantly inhibited TGF-β1-induced expression of EMT markers (E-cadherin reduction and vimentin induction) in 8505C cells in vitro. Treatment with EGCG completely blocked the phosphorylation of Smad2/3, translocation of Smad4. Taken together, these results suggest that EGCG suppresses EMT and invasion and migration by blocking TGFβ/Smad signaling pathways. Taylor & Francis 2019-07-16 /pmc/articles/PMC6650192/ /pubmed/31311401 http://dx.doi.org/10.1080/21655979.2019.1632669 Text en © 2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Paper Li, Tingting Zhao, Ning Lu, Jie Zhu, Qingli Liu, Xinfeng Hao, Fengyun Jiao, Xuelong Epigallocatechin gallate (EGCG) suppresses epithelial-Mesenchymal transition (EMT) and invasion in anaplastic thyroid carcinoma cells through blocking of TGF-β1/Smad signaling pathways |
title | Epigallocatechin gallate (EGCG) suppresses epithelial-Mesenchymal transition (EMT) and invasion in anaplastic thyroid carcinoma cells through blocking of TGF-β1/Smad signaling pathways |
title_full | Epigallocatechin gallate (EGCG) suppresses epithelial-Mesenchymal transition (EMT) and invasion in anaplastic thyroid carcinoma cells through blocking of TGF-β1/Smad signaling pathways |
title_fullStr | Epigallocatechin gallate (EGCG) suppresses epithelial-Mesenchymal transition (EMT) and invasion in anaplastic thyroid carcinoma cells through blocking of TGF-β1/Smad signaling pathways |
title_full_unstemmed | Epigallocatechin gallate (EGCG) suppresses epithelial-Mesenchymal transition (EMT) and invasion in anaplastic thyroid carcinoma cells through blocking of TGF-β1/Smad signaling pathways |
title_short | Epigallocatechin gallate (EGCG) suppresses epithelial-Mesenchymal transition (EMT) and invasion in anaplastic thyroid carcinoma cells through blocking of TGF-β1/Smad signaling pathways |
title_sort | epigallocatechin gallate (egcg) suppresses epithelial-mesenchymal transition (emt) and invasion in anaplastic thyroid carcinoma cells through blocking of tgf-β1/smad signaling pathways |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6650192/ https://www.ncbi.nlm.nih.gov/pubmed/31311401 http://dx.doi.org/10.1080/21655979.2019.1632669 |
work_keys_str_mv | AT litingting epigallocatechingallateegcgsuppressesepithelialmesenchymaltransitionemtandinvasioninanaplasticthyroidcarcinomacellsthroughblockingoftgfb1smadsignalingpathways AT zhaoning epigallocatechingallateegcgsuppressesepithelialmesenchymaltransitionemtandinvasioninanaplasticthyroidcarcinomacellsthroughblockingoftgfb1smadsignalingpathways AT lujie epigallocatechingallateegcgsuppressesepithelialmesenchymaltransitionemtandinvasioninanaplasticthyroidcarcinomacellsthroughblockingoftgfb1smadsignalingpathways AT zhuqingli epigallocatechingallateegcgsuppressesepithelialmesenchymaltransitionemtandinvasioninanaplasticthyroidcarcinomacellsthroughblockingoftgfb1smadsignalingpathways AT liuxinfeng epigallocatechingallateegcgsuppressesepithelialmesenchymaltransitionemtandinvasioninanaplasticthyroidcarcinomacellsthroughblockingoftgfb1smadsignalingpathways AT haofengyun epigallocatechingallateegcgsuppressesepithelialmesenchymaltransitionemtandinvasioninanaplasticthyroidcarcinomacellsthroughblockingoftgfb1smadsignalingpathways AT jiaoxuelong epigallocatechingallateegcgsuppressesepithelialmesenchymaltransitionemtandinvasioninanaplasticthyroidcarcinomacellsthroughblockingoftgfb1smadsignalingpathways |