Antimigratory Effects of the Methanol Extract from Momordica charantia on Human Lung Adenocarcinoma CL1 Cells

被引:16
作者
Hsu, Hsue-Yin [1 ,2 ]
Lin, Jung-Hsuan [1 ]
Li, Chia-Jung [2 ]
Tsang, Shih-Fang [3 ]
Tsai, Chun-Hao [1 ]
Chyuan, Jong-Ho [4 ]
Chiu, Shu-Jun [1 ]
Chuang, Shuang-En [5 ]
机构
[1] Tzu Chi Univ, Dept Life Sci, Hualien, Taiwan
[2] Tzu Chi Univ, Inst Med Sci, Hualien, Taiwan
[3] Tzu Chi Univ, Dept Anat, Hualien, Taiwan
[4] Hualien Dist Agr Res & Extens Stn, Hualien, Taiwan
[5] Natl Hlth Res Inst, Natl Inst Canc Res, Zhunan, Taiwan
关键词
FOCAL ADHESION KINASE; BETA-CATENIN; COLORECTAL-CANCER; HUMAN BREAST; ANTI-HIV; INHIBITION; WNT; MIGRATION; INVASION; OVEREXPRESSION;
D O I
10.1155/2012/819632
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Momordica charantia has been found to exhibit anticancer activity, in addition to its well-known therapeutic functions. We have demonstrated that the leaf extract of Momordica charantia (MCME) induces apoptosis in several human cancer cells through caspase-and mitochondria-dependent pathways. In this study, a different susceptibility to MCME was found in human lung adenocarcinoma CL1 cells with different metastatic ability, leading to the significant difference of cell viability and invasiveness betweenMCME-treated CL1-0 and CL1-5 cells. MCME was found to upregulate the expression of Wnt-2 and affect the migratory and invasive ability of CL1 cells through suppressed MMP-2 and MMP-9 enzymatic activities. We proposed that MCME mediates inhibition against migration of CL1 cells by reducing the expression and activation of Src and FAK to decrease the expression of downstream Akt, beta-catenin, and MMPs.
引用
收藏
页数:12
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