Abstract |
Prostate cancer (PCa) is a very prevalent male-specific malignancy; most PCa patients eventually die as a result of metastasis. L- theanine (C7H14N2O3), a nonprotein amino acid derivative from green tea leaves, has been demonstrated to act as an anticarcinogen through proapoptotic and antiproliferative effects. However, the antimetastatic effect of L- theanine in tumor cells and its underlying mechanism are still unclear. Here, we found that L- theanine could suppress invasion, migration, and increase cell-cell adhesion of prostate cancer cells in vitro and in vivo. We also found that L- theanine could inhibit the epithelial-mesenchymal transition process in PCa. Our study revealed that L- theanine could downregulate MMP9, N-cadherin, Vimentin, Snail, and upregulate E-cadherin. Furthermore, L- theanine suppressed the transcription of MMP9 and Snail by significantly inhibiting the ERK/NF-κB signaling pathway and the binding activity of p65 to the promoter regions of MMP9 and Snail. All of these findings suggest that L- theanine has therapeutic potential for metastatic PCa and may be considered a promising candidate for antimetastatic therapy of prostate cancer.
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Authors | Xirui Fan, Jinyi Zhou, Xiaowen Bi, Juanjuan Liang, Shuai Lu, Xintong Yan, Lan Luo, Zhimin Yin |
Journal | The Journal of nutritional biochemistry
(J Nutr Biochem)
Vol. 89
Pg. 108556
(03 2021)
ISSN: 1873-4847 [Electronic] United States |
PMID | 33249185
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2020 Elsevier Inc. All rights reserved. |
Chemical References |
- Antineoplastic Agents
- Cadherins
- Glutamates
- NF-kappa B
- Snail Family Transcription Factors
- Tea
- Vimentin
- theanine
- Matrix Metalloproteinase 9
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Topics |
- Animals
- Antineoplastic Agents
(metabolism, pharmacology)
- Cadherins
(metabolism)
- Cell Movement
(drug effects)
- Down-Regulation
- Epithelial-Mesenchymal Transition
(drug effects)
- Glutamates
(metabolism, pharmacology)
- Humans
- Male
- Matrix Metalloproteinase 9
(metabolism)
- Mice
- NF-kappa B
(metabolism)
- Neoplasm Metastasis
(pathology)
- PC-3 Cells
- Prostatic Neoplasms
(drug therapy, metabolism, pathology)
- Signal Transduction
(drug effects)
- Snail Family Transcription Factors
(metabolism)
- Tea
(chemistry)
- Vimentin
(metabolism)
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