Topoisomerase poisons differentially activate DNA damage checkpoints through ataxia-telangiectasia mutated–dependent and –independent mechanisms
| Autor: | Wai Yi, Siu, Anita, Lau, Talha, Arooz, Jeremy P H, Chow, Horace T B, Ho, Randy Y C, Poon |
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| Rok vydání: | 2004 |
| Předmět: |
G2 Phase
Cancer Research Cell Cycle Proteins Ataxia Telangiectasia Mutated Proteins Protein Serine-Threonine Kinases S Phase Caffeine Cell Line Tumor Guanine Nucleotide Exchange Factors Humans Topoisomerase II Inhibitors Enzyme Inhibitors Antibiotics Antineoplastic Cell Death Dose-Response Relationship Drug Tumor Suppressor Proteins Cell Cycle G1 Phase Nuclear Proteins DNA-Binding Proteins Genes cdc Oncology Doxorubicin Camptothecin Topoisomerase I Inhibitors DNA Damage |
| Zdroj: | Molecular Cancer Therapeutics. 3:621-632 |
| ISSN: | 1538-8514 1535-7163 |
| DOI: | 10.1158/1535-7163.621.3.5 |
| Popis: | Camptothecin and Adriamycin are clinically important inhibitors for topoisomerase (Topo) I and Topo II, respectively. The ataxia-telangiectasia mutated (ATM) product is essential for ionizing radiation-induced DNA damage responses, but the role of ATM in Topo poisons-induced checkpoints remains unresolved. We found that distinct mechanisms are involved in the activation of different cell cycle checkpoints at different concentrations of Adriamycin and camptothecin. Adriamycin promotes the G1 checkpoint through activation of the p53-p21CIP1/WAF1 pathway and decrease of pRb phosphorylation. Phosphorylation of p53(Ser20) after Adriamycin treatment is ATM dependent, but is not required for the full activation of p53. The G1 checkpoint is dependent on ATM at low doses but not at high doses of Adriamycin. In contrast, the Adriamycin-induced G2 checkpoint is independent on ATM but sensitive to caffeine. Adriamycin inhibits histone H3(Ser10) phosphorylation through inhibitory phosphorylation of CDC2 at low doses and down-regulation of cyclin B1 at high doses. The camptothecin-induced intra-S checkpoint is partially dependent on ATM, and is associated with inhibitory phosphorylation of cyclin-dependent kinase 2 and reduction of BrdUrd incorporation after mid-S phase. Finally, apoptosis associated with high doses of Adriamycin or camptothecin is not influenced by the absence of ATM. These data indicate that the involvement of ATM following treatment with Topo poisons differs extensively with dosage and for different cell cycle checkpoints. |
| Databáze: | OpenAIRE |
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