Delta-tocotrienol suppresses Notch-1 pathway by upregulating miR-34a in nonsmall cell lung cancer cells

被引:88
作者
Ji, Xiangming [1 ]
Wang, Zhiwei [2 ]
Geamanu, Andreea [1 ]
Goja, Arvind [1 ]
Sarkar, Fazlul H. [2 ]
Gupta, Smiti V. [1 ]
机构
[1] Wayne State Univ, Dept Nutr & Food Sci, Detroit, MI 48202 USA
[2] Wayne State Univ, Dept Pathol, Karmanos Canc Inst, Detroit, MI 48202 USA
关键词
delta-tocotrienol; miR-34a; Notch-1; non-small cell lung cancer; CYCLIN D1; POOR-PROGNOSIS; DOWN-REGULATION; GROWTH-FACTOR; OVEREXPRESSION; EXPRESSION; APOPTOSIS; MICRORNA-34A; SURVIVAL; P53;
D O I
10.1002/ijc.27549
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MicroRNAs (miRNAs) are small noncoding RNAs that play critical roles in regulating various cellular functions by transcriptional silencing. miRNAs can function as either oncogenes or tumor suppressors (oncomirs), depending on cancer types. In our study, using miRNA microarray, we observed that downregulation of the Notch-1 pathway, by delta-tocotrienol, correlated with upregulation of miR-34a, in nonsmall cell lung cancer cells (NSCLC). Moreover, re-expression of miR-34a by transfection in NSCLC cells resulted in inhibition of cell growth and invasiveness, induction of apoptosis and enhanced p53 activity. Furthermore, cellular mechanism studies revealed that induction of miR-34a decreased the expression of Notch-1 and its downstream targets including Hes-1, Cyclin D1, Survivin and Bcl-2. Our findings suggest that delta-tocotrienol is a nontoxic activator of mir-34a which can inhibit NSCLC cell proliferation, induce apoptosis and inhibit invasion, and thus offering a potential starting point for the design of novel anticancer agents.
引用
收藏
页码:2668 / 2677
页数:10
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