MEK-ERK-dependent multiple caspase activation by mitochondrial proapoptotic Bcl-2 family proteins is essential for heavy ion irradiation-induced glioma cell death
| Autor: | Jun Sunayama, Kenji Nemoto, Nomiya T, Shizuka Seino, Hidetoshi Yamashita, Arata Tomiyama, Yoshitaka Matsumoto, Atsushi Sato, Kenichiro Matsuda, Kyoko Suzuki, Takamasa Kayama, Ken Tachibana, Chifumi Kitanaka, Ando K |
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| Rok vydání: | 2011 |
| Předmět: |
MAPK/ERK pathway
Cancer Research Immunology bcl-X Protein Mitogen-activated protein kinase kinase Caspase 8 Cellular and Molecular Neuroscience Bcl-2-associated X protein Glioma Cell Line Tumor medicine Humans RNA Small Interfering Protein kinase A Extracellular Signal-Regulated MAP Kinases Caspase bcl-2-Associated X Protein Mitogen-Activated Protein Kinase Kinases biology apoptosis Cell Biology medicine.disease MAPK Cell biology Mitochondria bcl-2 Homologous Antagonist-Killer Protein Proto-Oncogene Proteins c-bcl-2 Apoptosis Caspases Cancer research biology.protein carbon beam RNA Interference Original Article heavy ion radiation |
| Zdroj: | Cell Death & Disease |
| ISSN: | 2041-4889 |
| Popis: | Recently developed heavy ion irradiation therapy using a carbon beam (CB) against systemic malignancy has numerous advantages. However, the clinical results of CB therapy against glioblastoma still have room for improvement. Therefore, we tried to clarify the molecular mechanism of CB-induced glioma cell death. T98G and U251 human glioblastoma cell lines were irradiated by CB, and caspase-dependent apoptosis was induced in both cell lines in a dose-dependent manner. Knockdown of Bax (BCL-2-associated X protein) and Bak (BCL-2-associated killer) and overexpression of Bcl-2 or Bcl-xl (B-cell lymphoma-extra large) showed the involvement of Bcl-2 family proteins upstream of caspase activation, including caspase-8, in CB-induced glioma cell death. We also detected the activation of extracellular signal-regulated kinase (ERK) and the knockdown of ERK regulator mitogen-activated protein kinase kinase (MEK)1/2 or overexpression of a dominant-negative (DN) ERK inhibited CB-induced glioma cell death upstream of the mitochondria. In addition, application of MEK-specific inhibitors for defined periods showed that the recovery of activation of ERK between 2 and 36 h after irradiation is essential for CB-induced glioma cell death. Furthermore, MEK inhibitors or overexpression of a DN ERK failed to significantly inhibit X-ray-induced T98G and U251 cell death. These results suggested that the MEK–ERK cascade has a crucial role in CB-induced glioma cell death, which is known to have a limited contribution to X-ray-induced glioma cell death. |
| Databáze: | OpenAIRE |
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