NaV1.5 enhances breast cancer cell invasiveness by increasing NHE1-dependent H+ efflux in caveolae

被引:148
作者
Brisson, L. [1 ]
Gillet, L. [1 ]
Calaghan, S. [2 ]
Besson, P. [1 ]
Le Guennec, J-Y [3 ]
Roger, S. [1 ]
Gore, J. [1 ]
机构
[1] Univ Tours, Fac Med, INSERM, U921, F-37032 Tours, Region Center, France
[2] Univ Leeds, Inst Syst & Membrane Biol, Leeds, W Yorkshire, England
[3] Univ Montpellier 2, INSERM, Physiopathol cardiovasc U637, Montpellier, France
关键词
cancer; caveolae; invasion; Na (broken vertical bar)/H (broken vertical bar) exchanger; voltage-gated sodium channels; GATED SODIUM-CHANNELS; CATHEPSIN-B; EXPRESSION; EXCHANGER;
D O I
10.1038/onc.2010.574
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Na(V)1.5 sodium channels enhance the invasiveness of breast cancer cells through the acidic-dependent activation of cysteine cathepsins. Here, we showed that the Na+/H+ exchanger type 1 (NHE1) was an important regulator of H+ efflux in breast cancer cells MDA-MB-231 and that its activity was increased by Na(V)1.5. Na(V)1.5 and NHE1 were colocalized in membrane rafts containing caveolin-1. The inhibition of Na(V)1.5 or NHE1 induced a similar reduction in cell invasiveness and extracellular matrix degradation; no additive effect was observed when they were simultaneously inhibited. Our study suggests that NaV1.5 and NHE1 are functionally coupled and enhance the invasiveness of cancer cells by increasing H+ efflux. Oncogene (2011) 30, 2070-2076; doi:10.1038/onc.2010.574; published online 20 December 2010
引用
收藏
页码:2070 / 2076
页数:7
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