Eckhardt, Alexander and Mueller, Philipp and Hiller, Karl-Anton and Krifka, Stephanie and Bolay, Carola and Spagnuolo, Gianrico and Schmalz, Gottfried and Schweikl, Helmut (2010) Influence of TEGDMA on the mammalian cell cycle in comparison with chemotherapeutic agents. DENTAL MATERIALS, 26 (3). pp. 232-241. ISSN 0109-5641, 1879-0097
Full text not available from this repository. (Request a copy)Abstract
Objectives. The dental resin monomer triethylene glycol dimethacrylate (TEGDMA) caused a cell cycle arrest in response to DNA damage. However, the underlying mechanisms are unclear. Therefore, the influence of TEGDMA on the cell cycle was analyzed in comparison with the chemotherapeutic agents adriamycin and mitomycin C (MMC), which arrest the cell cycle through different mechanisms. Methods. RAW264.7 mouse macrophages were exposed to TEGDMA, adriamycin, or MMC, and flow cytometry (FACS) was used for cell cycle analyses. In addition, the number of surviving cells was determined by a crystal violet assay, and viability in treated cultures was determined by FACS after staining of cells with trypan blue. Morphological changes in cells were interpreted using forward and side scatter (FSC/SSC) cell physical criteria. Results. The exposure of cells to 1 mM TEGDMA resulted in a delay of the cell cycle in G1 phase since 85.3% of the cells were found in G1 compared with 47.4% in untreated controls. Adriamycin also increased the number of cells (72.1%) in G1 compared to controls. Caffeine, an inhibitor of the checkpoint kinases ATM (ataxia telangiectasia-mutated) and ATR (ATM and Rad3-related), had no effect on the TEGDMA and adriamycin-induced cell cycle arrest. In contrast, MMC delayed the cell cycle in G2 since cell numbers increased to 22.1% compared to 10.7% in controls. The effect of MMC on G2 was even increased by low caffeine concentrations (100-400 mu M), but 1000 mu M caffeine inhibited MMC activity. Significance. Our results suggest that the mechanism of a TEGDMA-induced arrest of the cell cycle is different from the effect of the direct-acting interstrand crosslinking agent MMC. Since TEGDMA produced oxidative stress, it probably acts indirectly on the cell cycle through reactive oxygen species, unless TEGDMA-DNA adducts are shown experimentally. (C) 2009 Academy of Dental Materials. Published by Elsevier Ltd. All rights reserved.
| Item Type: | Article |
|---|---|
| Uncontrolled Keywords: | TRIETHYLENE GLYCOL DIMETHACRYLATE; OXIDATIVE DNA-DAMAGE; RESIN MONOMERS; MITOMYCIN-C; INDUCED APOPTOSIS; MAP-KINASES; TUMOR-CELLS; PULP CELLS; IN-VITRO; CAFFEINE; Dental resin; TEGDMA; Cell cycle; Adriamycin; Mitomycin C |
| Subjects: | 600 Technology > 610 Medical sciences Medicine |
| Divisions: | Medicine > Lehrstuhl für Zahnerhaltung und Parodontologie > Prof. Dr. rer. nat. Helmut Schweikl |
| Depositing User: | Dr. Gernot Deinzer |
| Date Deposited: | 05 Aug 2020 04:59 |
| Last Modified: | 05 Aug 2020 04:59 |
| URI: | https://pred.uni-regensburg.de/id/eprint/25023 |
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