Induction of p21Waf1/Cip1 by Garcinol via Downregulation of p38-MAPK Signaling in p53-Independent H1299 Lung Cancer

被引:47
作者
Yu, Sheng-Yung [1 ]
Liao, Chiung-Ho [2 ]
Chien, Ming-Hsien [3 ,4 ]
Tsai, Tsung-Yu [5 ]
Lin, Jen-Kun [6 ]
Weng, Meng-Shih [1 ]
机构
[1] Fu Jen Catholic Univ, Dept Nutr Sci, New Taipei City 24205, Taiwan
[2] Food & Drug Adm, Minist Hlth & Welf, Div Drug & New Technol Prod, Taipei 10058, Taiwan
[3] Taipei Med Univ, Coll Med, Grad Inst Clin Med, Taipei 110, Taiwan
[4] Taipei Med Univ, Wan Fang Hosp, Taipei 110, Taiwan
[5] Fu Jen Catholic Univ, Dept Food Sci, New Taipei City 24205, Taiwan
[6] Natl Taiwan Univ, Coll Med, Inst Biochem & Mol Biol, Taipei 10617, Taiwan
关键词
garcinol; lung cancer; p53; G1; arrest; p21(Waf1/Cip1); p38-MAPK; CELL-CYCLE; P53; APOPTOSIS; SUPPRESSION; PROLIFERATION; ACTIVATION; EXPRESSION; SURVIVAL; HISTONE; STRESS;
D O I
10.1021/jf4037722
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Garcinol, a polyisoprenylated benzophenone, from Garcinia indica fruit rind has possessed anti-inflammatory, antioxidant, antiproliferation, and anticancer activities. However, the anticancer mechanisms of garcinol in lung cancer were still unclear. Therefore, we examine the effects of garcinol on antiproliferation in human lung cancer cells. Treatments with garcinol for 24 h exhibited morphological changes and inhibited the proliferation of H460 (p53-wild type) and H1299 (p53-null) cells in dose- and time-dependent manners. Furthermore, a significant G1 cell cycle arrest was observed in a dose-dependent treatment after H1299 cells were exposed in garcinol, whereas garcinol induced apoptosis rather than cell cycle arrest in H460 cells. Moreover, cyclin-dependent kinase 2 (CDK2), cyclin-dependent kinase 4 (CDK4), cyclin D1, and cyclin D3 were decreased, although cyclin E and cyclin-dependent kinase 6 (CDK6) were increased in garcinol-treated H1299 cells. Meanwhile, the protein levels of CDK inhibitors p21(Waf1/Cip1) and p27(KIPI) also exhibited upregulation after garcinol treatments. The enhanced protein-associated level between p21(Waf1/Cip1) and CDK4/2 rather than p27(KIPI) and CDK4/2 was demonstrated in garcinol-treated cells. Additionally, knock-down p21(Waf1/Cip1) by specific siRNA competently prevented garcinol-induced G1 arrest. Besides, garcinol also inhibited ERK and p38-MAPK activations in time-dependent mode. The pretreatment with p38-MAPK inhibitor but not ERK inhibitor raised garcinol-induced G1 population cells. Co-treatment with p38-MAPK inhibitor and garcinol synergistically elevated cyclin E, p21(Waf1/Cip1), and p27(Kip1) expressions. Meanwhile, overexpression dominant negative p38-MAPK also enhanced garcinol-induced p21(Waf1/Cip1) expression in H1299 cells. Accordingly, our data suggested that garcinol induced G1 cell cycle arrest and apoptosis in lung cancer cells under different p53 statuses. The p53-independent G1 cell cycle arrest induced by garcinol might be through upregulation of p21(Waf1/Cip1) triggered from p38-MAPK signaling inactivation.
引用
收藏
页码:2085 / 2095
页数:11
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