Diss J K J, Fraser S P, Walker M M, Patel A, Latchman D S, Djamgoz M B A
Medical Molecular Biology Unit, Institute of Child Health, University College London, London, UK.
Prostate Cancer Prostatic Dis. 2008;11(4):325-33. doi: 10.1038/sj.pcan.4501012. Epub 2007 Sep 25.
We previously identified high levels of Na(v)1.7 voltage-gated sodium channel alpha-subunit (VGSCalpha) mRNA and protein in human prostate cancer cells and tissues. Here, we investigated auxillary beta-subunit (VGSCbetas) expression. In vitro, the combined expression of all four VGSCbetas was significantly (approximately 4.5-fold) higher in strongly compared to weakly metastatic cells. This was mainly due to increased beta1-expression, which was under androgenic control. In vivo, beta1-beta4 mRNAs were detectable and their expression in CaP vs non-CaP tissues generally reflected the in vitro levels in relation to metastatic potential. The possible role(s) of VGSCbetas (VGSCalpha-associated and VGSCalpha-independent) in prostate cancer are discussed.
我们之前在人前列腺癌细胞和组织中鉴定出高水平的Na(v)1.7电压门控钠通道α亚基(VGSCα)mRNA和蛋白质。在此,我们研究了辅助β亚基(VGSCβs)的表达。在体外,与低转移细胞相比,高转移细胞中所有四种VGSCβs的联合表达显著更高(约4.5倍)。这主要归因于β1表达的增加,其受雄激素控制。在体内,可检测到β1-β4 mRNA,它们在前列腺癌组织与非前列腺癌组织中的表达通常反映了与转移潜能相关的体外水平。本文讨论了VGSCβs(与VGSCα相关和与VGSCα无关)在前列腺癌中的可能作用。