Abstract |
This is the first study to demonstrate that the small-molecule Bcl-2 inhibitor HA14-1 renders human cervical cancer cells and their Bcl-2 overexpressing radioresistant counterparts, but not normal fibroblasts, more susceptible to heavy ions. Thus, Bcl-2 may be an attractive target for improving the efficacy of heavy-ion therapy.
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Authors | Nobuyuki Hamada, Keiko Kataoka, Sakura Sora, Takamitsu Hara, Motoko Omura-Minamisawa, Tomoo Funayama, Tetsuya Sakashita, Takashi Nakano, Yasuhiko Kobayashi |
Journal | Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology
(Radiother Oncol)
Vol. 89
Issue 2
Pg. 227-30
(Nov 2008)
ISSN: 0167-8140 [Print] Ireland |
PMID | 18774194
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Benzopyrans
- Nitriles
- Photosensitizing Agents
- Proto-Oncogene Proteins c-bcl-2
- ethyl 2-amino-6-bromo-4-(1-cyano-2-ethoxy-2-oxoethyl)-4H-chromene-3-carboxylate
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Topics |
- Benzopyrans
(pharmacology)
- Cell Death
(radiation effects)
- Cell Survival
(radiation effects)
- Female
- Fibroblasts
(radiation effects)
- Heavy Ions
- Humans
- Nitriles
(pharmacology)
- Photosensitizing Agents
(pharmacology)
- Proto-Oncogene Proteins c-bcl-2
(antagonists & inhibitors)
- Radiation Tolerance
- Radiation, Ionizing
- Tumor Cells, Cultured
- Uterine Cervical Neoplasms
(pathology, radiotherapy)
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