首页> 美国卫生研究院文献>Journal of Cancer >The Blockage of KCa3.1 Channel Inhibited Proliferation Migration and Promoted Apoptosis of Human Hepatocellular Carcinoma Cells
【2h】

The Blockage of KCa3.1 Channel Inhibited Proliferation Migration and Promoted Apoptosis of Human Hepatocellular Carcinoma Cells

机译:KCa3.1通道的阻滞抑制了人类肝癌细胞的增殖迁移和促凋亡。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。
获取外文期刊封面目录资料

摘要

The intermediate conductance calcium-activated potassium channel KCa3.1 plays an important role in regulating cell proliferation and migration. However, the role of KCa3.1 channel in human hepatocellular carcinoma remained unknown. This study was therefore performed to investigate the effects of KCa3.1 potassium channel blocker on the proliferation, apoptosis and migration of human hepatocellular cancer cells HepG2. KCa3.1 mRNA and protein were detected in HepG2. Furthermore, KCa3.1 potassium channel blocker TRAM-34 was capable to inhibit the proliferation and induce the apoptosis of HepG2 cells, which can be partially attenuated by 1-EBIO, an activator of KCa3.1 channel. Moreover, the migration of HepG2 was obviously inhibited by TRAM-34. Consistently, knockdown of KCa3.1 channel using its siRNA was also able to induce apoptosis and suppress proliferation and migration of HepG2. Meanwhile, intracellular ROS level was found augmented in HepG2 treated with TRAM-34. More importantly, p53 protein was found translocation from the cytoplasm into the nuclei of HepG2. Collectively, inhibition of KCa3.1 channel suppressed the growth and migration, and promoted the apoptosis of human hepatocellular carcinoma cells by regulating intracellular ROS level and promoting p53 activation. This data suggests TRAM-34 as a promising anti-tumor drug for liver cancer.
机译:中间电导钙激活钾通道KCa3.1在调节细胞增殖和迁移中起重要作用。然而,KCa3.1通道在人类肝细胞癌中的作用仍然未知。因此,进行该研究以研究KCa3.1钾通道阻滞剂对人肝癌细胞HepG2的增殖,凋亡和迁移的影响。在HepG2中检测到KCa3.1 mRNA和蛋白。此外,KCa3.1钾通道阻滞剂TRAM-34能够抑制HepG2细胞的增殖并诱导其凋亡,而HepG2细胞可以被1-CaIO(KCa3.1通道的激活剂)部分减弱。另外,TRAM-34明显抑制了HepG2的迁移。一致地,使用其siRNA敲除KCa3.1通道也能够诱导凋亡并抑制HepG2的增殖和迁移。同时,在用TRAM-34处理的HepG2中发现细胞内ROS水平升高。更重要的是,发现p53蛋白从细胞质易位到HepG2的细胞核中。总的来说,抑制KCa3.1通道可抑制生长和迁移,并通过调节细胞内ROS水平和促进p53活化来促进人肝癌细胞的凋亡。该数据表明TRAM-34是一种有前途的抗肝癌药物。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号