Keumsa Linteusan Suppresses Invasion of Cancer Cells through the Inhibition of Cellular Adhesion and MMP-9 Expression

被引:1
|
作者
Kim, Won-Jung [1 ]
Hong, Sung-Chang [2 ]
Do, Eun-Ju [3 ]
Suk, Kyungho [4 ]
Yun, Ik Jin [5 ]
Lee, Won-Ha [1 ]
机构
[1] Kyungpook Natl Univ, Sch Life Sci & Biotechnol, Taegu 702701, South Korea
[2] Zenitec Korea Co, Seoul 158732, South Korea
[3] Oriental Med Ind Support Ctr, Taegu 706828, South Korea
[4] Kyungpook Natl Univ, Sch Med, Dept Pharmacol, Taegu 702701, South Korea
[5] Konkuk Univ, Coll Med, Taegu 143702, South Korea
关键词
Linteusan; MMP-9; cancer; migration; adhesion; PHELLINUS-LINTEUS; CHRONIC INFLAMMATION; MUSHROOM; GROWTH; APOPTOSIS; POLYSACCHARIDES; MIGRATION; PI3K/AKT; KINASE; MACROPHAGES;
D O I
10.1080/19768354.2009.9647201
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Extracts derived from various medical mushrooms have been reported to have antitumor and immunomodulatory properties. In order to investigate the antitumor activity of keumsa Linteusan, the water extract of Phellinus limteus, HT1080 cells, a human fibrosarcoma cell line, were treated with it and changes in cellular migration potential was tested in vitro. At a concentration range below 1,000 mu g/mL, Linteusan blocked, in a dose dependent manner, the migration of cells through Matrigel as well as Boyden chamber without affecting the viability of the cells. Prolonged treatment of HT1080 cells with Linteusan suppressed TNF-alpha induced production of matrix metalloproteinase (MMP)-9 as well as basal level expression of MMP-2. Linteusan also affected the adhesion of the cells to fibronectin-coated surfaces. The effect of Linteusan on cell signaling pathways was also tested. Linteusan specifically affected TNF-alpha induced phosphorylation of AKT in a dose-dependent manner, while phosphorylation levels of ERK remained unaffected. These data indicate that Linteusan blocks the migration of HT1080 cells by affecting various processes associated with cell migration such as the expression of matrix degrading enzymes, cell adhesion, and AKT-medicated cellular signaling pathways.
引用
收藏
页码:113 / 118
页数:6
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