Abstract | BACKGROUND: MATERIALS AND METHODS: Radio-sensitization to carbon-ion radiotherapy when combined with a novel HDACI cyclic hydroxamic-acid-containing peptide 31(CHAP31) was assessed in human esophageal SCC both in vitro and in vivo. Changes of expression of genes related to DNA repair, by CHAP31 were assessed by quantitative real-time reverse transcriptional PCR analysis. RESULTS: CHAP31 induced sensitization to carbon-ion radiotherapy in vitro and tumor growth was significantly suppressed by the combination of carbon-ion radiotherapy with CHAP31 in comparison to either agent alone in in vivo experiments. CHAP31 inhibited the expression of genes related to DNA repair. CONCLUSION: CHAP31 sensitizes SCC cells to carbon-ion radiotherapy and this combinatory treatment may be a potentially useful therapeutic strategy for esophageal SCC.
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Authors | Masayuki Kano, Shigeru Yamada, Isamu Hoshino, Kentaro Murakami, Yasunori Akutsu, Haruhito Sakata, Takanori Nishimori, Akihiro Usui, Yukimasa Miyazawa, Tadashi Kamada, Hirohiko Tsujii, Hisahiro Matsubara |
Journal | Anticancer research
(Anticancer Res)
Vol. 29
Issue 11
Pg. 4433-8
(Nov 2009)
ISSN: 1791-7530 [Electronic] Greece |
PMID | 20032389
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Histone Deacetylase Inhibitors
- Peptides, Cyclic
- cyclic hydroxamic acid-containing peptide 31
- Carbon
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Topics |
- Animals
- Carbon
(chemistry)
- Carcinoma, Squamous Cell
(drug therapy, enzymology, genetics, radiotherapy)
- Cell Line, Tumor
- Combined Modality Therapy
- DNA Repair
(genetics)
- Esophageal Neoplasms
(drug therapy, enzymology, genetics, radiotherapy)
- Gene Expression
(drug effects, radiation effects)
- Heavy Ion Radiotherapy
- Histone Deacetylase Inhibitors
(pharmacology)
- Humans
- Male
- Mice
- Mice, Inbred BALB C
- Mice, Nude
- Peptides, Cyclic
(pharmacology)
- Xenograft Model Antitumor Assays
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