Abstract | PURPOSE: Methylation of H3 at lysine 4 (H3 Lys4) may be correlated with active gene trascription, whereas methylation of H3 at lysine 9 (H3 Lys9) may be linked to gene repression in murine cells and Schizosaccharomyces pombe. METHODS: Using Western blot analysis, heat-induced changes were studied in two human oral cancer cell lines, HSC4 (thermoresistant cells) and KB (thermosensitive cells). Histone H3 changes were studied; in particular for H3-Lys4 and H3-Lys9 methylation combined with KNK437. RESULTS: Heating of HSC4 cells at 45 degrees C for 20 min and KB cells for 3 min gradually increased H3-Lys4 and H3-Lys9 methylation. Treatment of both cells with 100 microM KNK437 before or after heat-treatment inhibited methylation of H3-Lys4, while methylation of H3 Lys9 remained unaffected. Use of KNK437 either before or after heat treatment inhibited the expression of HSP70. CONCLUSIONS: The findings suggest that heat-induced methylation of histone H3 may be correlated with the induction of HSPs by heating.
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Authors | Keiji Matsuda, Shin-Ya Nakagawa, Tomoya Nakano, Jun-Ichi Asaumi, Ganesh Chandra Jagetia, Shoji Kawasaki |
Journal | International journal of hyperthermia : the official journal of European Society for Hyperthermic Oncology, North American Hyperthermia Group
(Int J Hyperthermia)
Vol. 22
Issue 8
Pg. 729-35
(Dec 2006)
ISSN: 0265-6736 [Print] England |
PMID | 17391001
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Benzhydryl Compounds
- Heat-Shock Proteins
- Histones
- KNK 437
- Pyrrolidinones
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Topics |
- Benzhydryl Compounds
(pharmacology)
- Cell Line, Tumor
- Heat-Shock Proteins
(antagonists & inhibitors)
- Histones
(chemistry, drug effects)
- Humans
- Hyperthermia, Induced
(adverse effects)
- KB Cells
- Methylation
- Mouth Neoplasms
(therapy)
- Neoplasms, Squamous Cell
(therapy)
- Pyrrolidinones
(pharmacology)
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