Honokiol, a chemopreventive agent against skin cancer, induces cell cycle arrest and apoptosis in human epidermoid A431 cells

被引:26
|
作者
Chilampalli, Chandeshwari [1 ]
Guillermo, Ruth [1 ]
Kaushik, Radhey S. [2 ,3 ]
Young, Alan [3 ]
Chandrasekher, Gudiseva [1 ]
Fahmy, Hesham [1 ]
Dwivedi, Chandradhar [1 ]
机构
[1] S Dakota State Univ, Dept Pharmaceut Sci, Brookings, SD 57007 USA
[2] S Dakota State Univ, Dept Biol & Microbiol, Brookings, SD 57007 USA
[3] S Dakota State Univ, Dept Vet & Biomed Sci, Brookings, SD 57007 USA
关键词
honokiol; apoptosis; cell cycle; GROWTH; REGULATORS; PHOTOCARCINOGENESIS; CHECKPOINTS; ACTIVATION; INHIBITORS; CASPASE-3; PATHWAY; CASCADE;
D O I
10.1258/ebm.2011.011030
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Honokiol is a plant lignan isolated from bark and seed cones of Magnolia officinalis. Recent studies from our laboratory indicated that honokiol pretreatment decreased ultraviolet B-induced skin cancer development in SKH-1 mice. The aim of the present investigation was to study the effects of honokiol on human epidermoid squamous carcinoma A431 cells and to elucidate possible mechanisms involved in preventing skin cancer. A431 cells were pretreated with different concentrations of honokiol for a specific time period and investigated for effects on apoptosis and cell cycle analysis. Treatment with honokiol significantly decreased cell viability and cell proliferation in a concentration- and time-dependent manner. Honokiol pretreatment at 50 mu mol/L concentration induced G0/G1 cell cycle arrest significantly (P < 0.05) and decreased the percentage of cells in the S and G2/M phase. Honokiol down-regulated the expression of cyclin D1, cyclin D2, Cdk2, Cdk4 and Cdk6 proteins and up-regulated the expression of Cdk's inhibitor proteins p21 and p27. Pretreatment of A431 cells with honokiol leads to induction of apoptosis and DNA fragmentation. These findings indicate that honokiol provides its effects in squamous carcinoma cells by inducing cell cycle arrest at G0/G1 phase and apoptosis.
引用
收藏
页码:1351 / 1359
页数:9
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