HERG K+ channel-dependent apoptosis and cell cycle arrest in human glioblastoma cells.
Glioblastoma (GB) is associated with poor patient survival owing to uncontrolled tumor proliferation and resistance to apoptosis. Human ether-a-go-go-related gene K(+) channels (hERG; Kv11.1, KCNH2) are expressed in multiple cancer cells including GB and control cell proliferation and death. We hypo...
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doaj-a8629f74b84f412e92a180c256be423a2021-03-03T20:16:13ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-0192e8816410.1371/journal.pone.0088164HERG K+ channel-dependent apoptosis and cell cycle arrest in human glioblastoma cells.Ingo StaudacherJulian JehleKathrin StaudacherHans-Werner PledlDieter LemkePatrick A SchweizerRüdiger BeckerHugo A KatusDierk ThomasGlioblastoma (GB) is associated with poor patient survival owing to uncontrolled tumor proliferation and resistance to apoptosis. Human ether-a-go-go-related gene K(+) channels (hERG; Kv11.1, KCNH2) are expressed in multiple cancer cells including GB and control cell proliferation and death. We hypothesized that pharmacological targeting of hERG protein would inhibit tumor growth by inducing apoptosis of GB cells. The small molecule hERG ligand doxazosin induced concentration-dependent apoptosis of human LNT-229 (EC50 = 35 µM) and U87MG (EC50 = 29 µM) GB cells, accompanied by cell cycle arrest in the G0/G1 phase. Apoptosis was associated with 64% reduction of hERG protein. HERG suppression via siRNA-mediated knock down mimicked pro-apoptotic effects of doxazosin. Antagonism of doxazosin binding by the non-apoptotic hERG ligand terazosin resulted in rescue of protein expression and in increased survival of GB cells. At the molecular level doxazosin-dependent apoptosis was characterized by activation of pro-apoptotic factors (phospho-erythropoietin-producing human hepatocellular carcinoma receptor tyrosine kinase A2, phospho-p38 mitogen-activated protein kinase, growth arrest and DNA damage inducible gene 153, cleaved caspases 9, 7, and 3), and by inactivation of anti-apoptotic poly-ADP-ribose-polymerase, respectively. In summary, this work identifies doxazosin as small molecule compound that promotes apoptosis and exerts anti-proliferative effects in human GB cells. Suppression of hERG protein is a crucial molecular event in GB cell apoptosis. Doxazosin and future derivatives are proposed as novel options for more effective GB treatment.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24516604/pdf/?tool=EBI |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Ingo Staudacher Julian Jehle Kathrin Staudacher Hans-Werner Pledl Dieter Lemke Patrick A Schweizer Rüdiger Becker Hugo A Katus Dierk Thomas |
spellingShingle |
Ingo Staudacher Julian Jehle Kathrin Staudacher Hans-Werner Pledl Dieter Lemke Patrick A Schweizer Rüdiger Becker Hugo A Katus Dierk Thomas HERG K+ channel-dependent apoptosis and cell cycle arrest in human glioblastoma cells. PLoS ONE |
author_facet |
Ingo Staudacher Julian Jehle Kathrin Staudacher Hans-Werner Pledl Dieter Lemke Patrick A Schweizer Rüdiger Becker Hugo A Katus Dierk Thomas |
author_sort |
Ingo Staudacher |
title |
HERG K+ channel-dependent apoptosis and cell cycle arrest in human glioblastoma cells. |
title_short |
HERG K+ channel-dependent apoptosis and cell cycle arrest in human glioblastoma cells. |
title_full |
HERG K+ channel-dependent apoptosis and cell cycle arrest in human glioblastoma cells. |
title_fullStr |
HERG K+ channel-dependent apoptosis and cell cycle arrest in human glioblastoma cells. |
title_full_unstemmed |
HERG K+ channel-dependent apoptosis and cell cycle arrest in human glioblastoma cells. |
title_sort |
herg k+ channel-dependent apoptosis and cell cycle arrest in human glioblastoma cells. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS ONE |
issn |
1932-6203 |
publishDate |
2014-01-01 |
description |
Glioblastoma (GB) is associated with poor patient survival owing to uncontrolled tumor proliferation and resistance to apoptosis. Human ether-a-go-go-related gene K(+) channels (hERG; Kv11.1, KCNH2) are expressed in multiple cancer cells including GB and control cell proliferation and death. We hypothesized that pharmacological targeting of hERG protein would inhibit tumor growth by inducing apoptosis of GB cells. The small molecule hERG ligand doxazosin induced concentration-dependent apoptosis of human LNT-229 (EC50 = 35 µM) and U87MG (EC50 = 29 µM) GB cells, accompanied by cell cycle arrest in the G0/G1 phase. Apoptosis was associated with 64% reduction of hERG protein. HERG suppression via siRNA-mediated knock down mimicked pro-apoptotic effects of doxazosin. Antagonism of doxazosin binding by the non-apoptotic hERG ligand terazosin resulted in rescue of protein expression and in increased survival of GB cells. At the molecular level doxazosin-dependent apoptosis was characterized by activation of pro-apoptotic factors (phospho-erythropoietin-producing human hepatocellular carcinoma receptor tyrosine kinase A2, phospho-p38 mitogen-activated protein kinase, growth arrest and DNA damage inducible gene 153, cleaved caspases 9, 7, and 3), and by inactivation of anti-apoptotic poly-ADP-ribose-polymerase, respectively. In summary, this work identifies doxazosin as small molecule compound that promotes apoptosis and exerts anti-proliferative effects in human GB cells. Suppression of hERG protein is a crucial molecular event in GB cell apoptosis. Doxazosin and future derivatives are proposed as novel options for more effective GB treatment. |
url |
https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24516604/pdf/?tool=EBI |
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