MycN promotes TRPM7 expression and cell migration in neuroblastoma through a process that involves polyamines

被引:10
|
作者
Lange, Ingo [1 ]
Koomoa, Dana-Lynn T. [1 ]
机构
[1] Univ Hawaii, Daniel K Inouye Coll Pharm, Hilo, HI 96720 USA
来源
FEBS OPEN BIO | 2014年 / 4卷
基金
美国国家卫生研究院;
关键词
TRPM7; Neuroblastoma; MycN; Migration; Polyamines; BREAST-CANCER CELLS; N-MYC; ORNITHINE-DECARBOXYLASE; CALCIUM-CHANNEL; KINASE DOMAIN; ION-CHANNEL; AMPLIFICATION; ORAI3; PROLIFERATION; PROGRESSION;
D O I
10.1016/j.fob.2014.10.012
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Neuroblastoma is an extra-cranial solid cancer in children. MYCN gene amplification is a prognostic indicator of poor outcome in neuroblastoma. Recent studies have shown that the multiple steps involved in cell migration are dependent on the availability of intracellular calcium (Ca2+). Although significant advances have been made in understanding the role of Ca2+ during migration, little has been achieved towards understanding its impact on the progression of diseases such as cancer. Interestingly, previous studies showed that cancer cell migration is regulated by TRPM7, a calcium- permeable ion channel. The objective of the current study was to elucidate the mechanism by which MycN promotes NB cell migration and the mechanism regulating TRPM7 expression. The results showed that MycN increased TRPM7 expression, induced TRPM7 channel activity, increased intracellular Ca2+ signaling, and promoted cell migration in NB cells. The results also showed that inhibition or down-regulation of ornithine decarboxylase (ODC) inhibited TRPM7 expression, a process that was reversed by spermidine. Overall, this study provides evidence that MycN promotes TRPM7 expression and cell migration through a mechanism that involves ODC synthesis of polyamines. (C) 2014 The Authors. Published by Elsevier B.V. on behalf of the Federation of European Biochemical Societies.
引用
收藏
页码:966 / 975
页数:10
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