Pardo L A, Contreras-Jurado C, Zientkowska M, Alves F, Stühmer W
Max-Planck-Institute of Experimental Medicine, Hermann Rein Str. 3, Göttingen, 37075 Germany.
J Membr Biol. 2005 Jun;205(3):115-24. doi: 10.1007/s00232-005-0776-1.
Ion channels are being associated with a growing number of diseases including cancer. This overview summarizes data on voltage-gated potassium channels (VGKCs) that exhibit oncogenic properties: ether-à-go-go type 1 (Eag1). Normally, Eag1 is expressed almost exclusively in tissue of neural origin, but its ectopic expression leads to uncontrolled proliferation, while inhibition of Eag1 expression produces a concomitant reduction in proliferation. Specific monoclonal antibodies against Eag1 recognize an epitope in over 80% of human tumors of diverse origins, endowing it with diagnostic and therapeutic potential. Eag1 also possesses unique electrophysiological properties that simplify its identification. This is particularly important, as specific blockers of Eag1 currents are not available. Molecular imaging of Eag1 in live tumor models has been accomplished with dye-tagged antibodies using 3-D imaging techniques in the near-infrared spectral range.
离子通道与包括癌症在内的越来越多的疾病有关。本综述总结了关于具有致癌特性的电压门控钾通道(VGKC)的数据:即外向整流钾通道1型(Eag1)。正常情况下,Eag1几乎只在神经源性组织中表达,但其异位表达会导致不受控制的增殖,而抑制Eag1表达会使增殖随之减少。针对Eag1的特异性单克隆抗体在超过80%的不同起源的人类肿瘤中识别出一个表位,赋予其诊断和治疗潜力。Eag1还具有独特的电生理特性,便于对其进行识别。这一点尤为重要,因为目前尚无Eag1电流的特异性阻滞剂。在活体肿瘤模型中,已使用近红外光谱范围内的三维成像技术,通过染料标记抗体完成了Eag1的分子成像。