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Research ArticleExperimental Studies

Facilitation of H2O2-induced A172 Human Glioblastoma Cell Death by Insertion of Oxidative Stress-sensitive TRPM2 Channels

MASAKAZU ISHII, AKINORI OYAMA, TAMIO HAGIWARA, AKIRA MIYAZAKI, YASUO MORI, YUJI KIUCHI and SHUNICHI SHIMIZU
Anticancer Research November 2007, 27 (6B) 3987-3992;
MASAKAZU ISHII
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AKINORI OYAMA
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TAMIO HAGIWARA
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AKIRA MIYAZAKI
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YASUO MORI
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YUJI KIUCHI
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SHUNICHI SHIMIZU
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  • For correspondence: shun{at}pharm.showa-u.ac.jp
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Abstract

The melastatin-like transient receptor potential M2 (TRPM2) channel is a Ca2+ permeable channel that is activated by reactive oxygen species (ROS), and its activation induces necrotic cell death. The effect of insertion of TRPM2 into A172 human glioblastoma cells (A172 cells) was investigated. The insertion of TRPM2 channels enhanced cell death induced by H2O2 in the A172 cells. An H2O2-induced Ca2+ increase was observed in TRPM2-expressing cells, but not in wild-type cells. Proliferation, migration and invasion activities were not affected by the expression of TRPM2. TRPM2 seems to be a candidate for gene therapy in glioblastoma cells, since the insertion of TRPM2 into A172 cells can facilitate cell death through Ca2+ increase after H2O2 treatment without increasing malignancy.

  • H2O2
  • glioblastoma
  • TRPM2
  • calcium
  • cell death

Footnotes

  • Received August 1, 2007.
  • Revision received October 9, 2007.
  • Accepted October 24, 2007.
  • Copyright© 2007 International Institute of Anticancer Research (Dr. John G. Delinassios), All rights reserved
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Anticancer Research
Vol. 27, Issue 6B
November-December 2007
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Facilitation of H2O2-induced A172 Human Glioblastoma Cell Death by Insertion of Oxidative Stress-sensitive TRPM2 Channels
MASAKAZU ISHII, AKINORI OYAMA, TAMIO HAGIWARA, AKIRA MIYAZAKI, YASUO MORI, YUJI KIUCHI, SHUNICHI SHIMIZU
Anticancer Research Nov 2007, 27 (6B) 3987-3992;

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Facilitation of H2O2-induced A172 Human Glioblastoma Cell Death by Insertion of Oxidative Stress-sensitive TRPM2 Channels
MASAKAZU ISHII, AKINORI OYAMA, TAMIO HAGIWARA, AKIRA MIYAZAKI, YASUO MORI, YUJI KIUCHI, SHUNICHI SHIMIZU
Anticancer Research Nov 2007, 27 (6B) 3987-3992;
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