Novel roles for hERG K+ channels in cell proliferation and apoptosis

被引:0
|
作者
J Jehle
P A Schweizer
H A Katus
D Thomas
机构
[1] Medical University Hospital,Department of Cardiology
来源
Cell Death & Disease | 2011年 / 2卷
关键词
hERG; K; channel; cell proliferation; apoptosis; anticancer therapy;
D O I
暂无
中图分类号
学科分类号
摘要
The human ether-a-go-go-related gene potassium channel (hERG, Kv11.1, KCNH2) has an essential role in cardiac action potential repolarization. Electrical dysfunction of the voltage-sensitive ion channel is associated with potentially lethal ventricular arrhythmias in humans. hERG K+ channels are also expressed in a variety of cancer cells where they control cell proliferation and apoptosis. In this review, we discuss molecular mechanisms of hERG-associated cell cycle regulation and cell death. In addition, the significance of hERG K+ channels as future drug target in anticancer therapy is highlighted.
引用
收藏
页码:e193 / e193
相关论文
共 50 条
  • [31] Blockade of human HERG K+ channels by rosiglitazone, an antidiabetic drug
    Seung Ho Lee
    Min Ji Sung
    Sang June Hahn
    Jimok Kim
    Gyesik Min
    Su-Hyun Jo
    Han Choe
    Bok Hee Choi
    Archives of Pharmacal Research, 2012, 35 : 1655 - 1664
  • [32] Towards a Structural View of Drug Binding to hERG K+ Channels
    Vandenberg, Jamie I.
    Perozo, Eduardo
    Allen, Toby W.
    TRENDS IN PHARMACOLOGICAL SCIENCES, 2017, 38 (10) : 899 - 907
  • [33] Idiosyncratic gating of HERG-like K+ channels in microglia
    Pennefather, PS
    Zhou, W
    DeCoursey, TE
    JOURNAL OF GENERAL PHYSIOLOGY, 1998, 111 (06): : 795 - 805
  • [34] Structural basis of drug binding to hERG K+ channels.
    Sanguinetti, Michael C.
    CHEMICAL RESEARCH IN TOXICOLOGY, 2006, 19 (12) : 1685 - 1685
  • [35] Blockade of human HERG K+ channels by rosiglitazone, an antidiabetic drug
    Lee, Seung Ho
    Sung, Min Ji
    Hahn, Sang June
    Kim, Jimok
    Min, Gyesik
    Jo, Su-Hyun
    Choe, Han
    Choi, Bok Hee
    ARCHIVES OF PHARMACAL RESEARCH, 2012, 35 (09) : 1655 - 1664
  • [36] Single HERG K+ channels expressed in Xenopus oocytes.
    Zou, A
    Curran, ME
    Keating, MT
    Sanguinetti, MC
    BIOPHYSICAL JOURNAL, 1997, 72 (02) : TH148 - TH148
  • [37] Drug trapping in hERG K+ channels: (not) a matter of drug size?
    Linder, Tobias
    Bernsteiner, Harald
    Saxena, Priyanka
    Bauer, Florian
    Erker, Thomas
    Timin, Eugen
    Hering, Steffen
    Stary-Weinzinger, Anna
    MEDCHEMCOMM, 2016, 7 (03) : 512 - 518
  • [38] Blockade of HERG Human K+ Channels by the Antidepressant Drug Paroxetine
    Lee, Seung Ho
    Sung, Min Ji
    Lee, Hyang Mi
    Chu, Daehyun
    Hahn, Sang June
    Jo, Su-Hyun
    Choe, Han
    Choi, Bok Hee
    BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2014, 37 (09) : 1495 - 1504
  • [39] hERG K+ Channels Promote Survival of Irradiated Leukemia Cells
    Palme, Daniela
    Misovic, Milan
    Ganser, Katrin
    Klumpp, Lukas
    Salih, Helmut R.
    Zips, Daniel
    Huber, Stephan M.
    FRONTIERS IN PHARMACOLOGY, 2020, 11
  • [40] Inhibition of HERG1 K+ channels by the novel second-generation antihistamine mizolastine
    Taglialatela, M
    Pannaccione, A
    Castaldo, P
    Giorgio, G
    Annunziato, L
    BRITISH JOURNAL OF PHARMACOLOGY, 2000, 131 (06) : 1081 - 1088