Decreased intracellular chloride enhances cell migration and invasion via activation of the ERK1/2 signaling pathway in DU145 human prostate carcinoma cells

被引:2
|
作者
Sato, Junichi [1 ]
Nakano, Koya [1 ]
Miyazaki, Hiroaki [1 ]
机构
[1] Setsunan Univ, Fac Sci & Engn, Dept Life Sci, Neyagawa, Osaka 5728508, Japan
关键词
Prostate cancer; DU145; Migration; Invasion; ERK1/2; MMP-1; ION CHANNELS; CANCER CELLS; OVER-EXPRESSION; RAS ACTIVATION; GROWTH; PROLIFERATION; PROMOTES; COTRANSPORTER; PROGRESSION; INHIBITION;
D O I
10.1016/j.bbrc.2023.149170
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
Our previous study revealed that changes of the intracellular Cl-concentration ([Cl- ]i) affected cell proliferation in cancer cells. However, the role of Cl-on cell migration and invasion in cancer cells remains unanalyzed. Therefore, the aim of the present study is to investigate whether changes of [Cl- ]i affects cell migration and invasion of cancer cells. In human prostate cancer DU145 cells, cell migration and invasion were enhanced by culturing in the low Cl- medium (replacement of Cl- by NO3 - ). We also found that DU145 cells in the low Clcondition caused significant transient ERK1/2 activation followed by an increase of MMP-1 mRNA levels. Inhibition of ERK1/2 activation in the low Cl-condition reduced enhancement of MMP-1 mRNA levels and decreased cell migration and invasion. These observations indicate that [Cl- ]i plays important roles in metastatic function by regulating the ERK1/2 signaling pathway in human prostate cancer cells, and intracellular Cl-would be one of the key targets for anti-cancer therapy.
引用
收藏
页数:9
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