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  1. Home
  2. College of Oral Medicine /口腔醫學院
  3. Institute of Oral Sciences/口腔科學研究所
  4. Protective Effect of Alpha-Linolenic Acid on Human Oral Squamous Cell Carcinoma Metastasis and Apoptotic Cell Death
 
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Protective Effect of Alpha-Linolenic Acid on Human Oral Squamous Cell Carcinoma Metastasis and Apoptotic Cell Death

Journal
Nutrients
Journal Volume
15
Journal Issue
23
Start Page
4992
ISSN
2072-6643
Date Issued
2023-12-01
Author(s)
Ching-Chyuan Su
Cheng-Chia Yu  
Yi-Wen Shih
Kai-Li Liu  
Haw-Wen Chen
Chih-Chung Wu
Ya-Chen Yang
En-Ling Yeh
Chien-Chun Li  
DOI
10.3390/nu15234992
URI
https://scholars.csmu.edu.tw/handle/123456789/3350
Abstract
<jats:p>Oral cancer ranks sixth among Taiwan’s top 10 cancers and most patients with poor prognosis acquire metastases. The essential fatty acid alpha-linolenic acid (ALA) has been found to diminish many cancer properties. However, the anti-cancer activity of ALA in oral cancer has yet to be determined. We examined the mechanisms underlying ALA inhibition of metastasis and induction of apoptotic cell death in oral squamous cell carcinoma (OSCC). Migration and invasion assays confirmed the cancer cells’ EMT capabilities, whereas flow cytometry and Western blotting identified molecular pathways in OSCC. ALA dramatically reduced cell growth in a concentration-dependent manner according to the findings. Low concentrations of ALA (100 or 200 μM) inhibit colony formation, the expression of Twist and EMT-related proteins, the expression of MMP2/-9 proteins, and enzyme activity, as well as cell migration and invasion. Treatment with high concentrations of ALA (200 or 400 μM) greatly increases JNK phosphorylation and c-jun nuclear accumulation and then upregulates the FasL/caspase8/caspase3 and Bid/cytochrome c/caspase9/caspase3 pathways, leading to cell death. Low concentrations of ALA inhibit SAS and GNM cell migration and invasion by suppressing Twist and downregulating EMT-related proteins or by decreasing the protein expression and enzyme activity of MMP-2/-9, whereas high concentrations of ALA promote apoptosis by activating the JNK/FasL/caspase 8/caspase 3-extrinsic pathway and the Bid/cytochrome c/caspase 9 pathway. ALA demonstrates potential as a treatment for OSCC patients.</jats:p>
SDGs

[SDGs]SDG3

[SDGs]SDG10

Publisher
MDPI AG
Type
journal-article
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