首页> 美国卫生研究院文献>International Journal of Molecular Sciences >Serum Starvation-Induced Voltage-Gated Potassium Channel Kv7.5 Expression and Its Regulation by Sp1 in Canine Osteosarcoma Cells
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Serum Starvation-Induced Voltage-Gated Potassium Channel Kv7.5 Expression and Its Regulation by Sp1 in Canine Osteosarcoma Cells

机译:血清饥饿诱导的电压门控钾通道Kv7.5表达及Sp1在犬骨肉瘤细胞中的调控作用

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摘要

The KCNQ gene family, whose members encode Kv7 channels, belongs to the voltage-gated potassium (Kv) channel group. The roles of this gene family have been widely investigated in nerve and muscle cells. In the present study, we investigated several characteristics of Kv7.5, which is strongly expressed in the canine osteosarcoma cell line, CCL-183. Serum starvation upregulated Kv7.5 expression, and the Kv7 channel opener, flupirtine, attenuated cell proliferation by arresting cells in the G0/G1 phase. We also showed that Kv7.5 knockdown helps CCL-183 cells to proliferate. In an effort to find an endogenous regulator of Kv7.5, we used mithramycin A to reduce the level of the transcription factor Sp1, and it strongly inhibited the induction of Kv7.5 in CCL-183 cells. These results suggest that the activation of Kv7.5 by flupirtine may exert an anti-proliferative effect in canine osteosarcoma. Therefore, Kv7.5 is a possible molecular target for canine osteosarcoma therapy.
机译:KCNQ基因家族的成员编码Kv7通道,属于电压门控钾(Kv)通道组。该基因家族的作用已在神经和肌肉细胞中得到广泛研究。在本研究中,我们研究了在犬骨肉瘤细胞系CCL-183中强烈表达的Kv7.5的几个特征。血清饥饿会上调Kv7.5表达,而Kv7通道开放剂氟吡汀可将细胞停滞在G0 / G1期,从而减弱细胞增殖。我们还显示Kv7.5敲低有助于CCL-183细胞增殖。为了寻找内源性Kv7.5调节剂,我们使用了光神霉素A来降低转录因子Sp1的水平,并强烈抑制了CCL-183细胞中Kv7.5的诱导。这些结果表明氟吡汀激活Kv7.5可能在犬骨肉瘤中发挥抗增殖作用。因此,Kv7.5是犬骨肉瘤治疗的可能分子靶标。

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