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L-theanine suppresses the metastasis of prostate cancer by downregulating MMP9 and Snail.

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.
AuthorsXirui Fan, Jinyi Zhou, Xiaowen Bi, Juanjuan Liang, Shuai Lu, Xintong Yan, Lan Luo, Zhimin Yin
JournalThe Journal of nutritional biochemistry (J Nutr Biochem) Vol. 89 Pg. 108556 (03 2021) ISSN: 1873-4847 [Electronic] United States
PMID33249185 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 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
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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