Quantification and repair of psoralen-induced interstrand crosslinks in human cells

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• 作者：Daniel Vare^a ; ^{daniel.vare@su.se" class="auth_mail} ; ^{daniel@vare.eu" class="auth_mail} ; Fredrik Johansson^a ; Jan-Olov Persson^b ; Klaus Erixon^a ; Dag Jenssen^a
• 关键词：DNA repair ; DNA interstrand crosslinks ; ICL ; Psoralen ; Furocoumarins
• 刊名：Toxicology Letters
• 出版年：2 May, 2014
• 年：2014
• 卷：226
• 期：3
• 页码：343-350
• 全文大小：696 K

文摘

Bi-functional alkylating agents that cause crosslinks are commonly used in chemotherapy. However, there is no conclusive knowledge for human cells regarding the number of induced interstrand crosslinks (ICLs) and the unhooking rate when the lesion is removed from one of the DNA strand. Using a newly developed method, we quantified the number of induced ICLs for the five furocoumarins; psoralen, 5-methoxypsoralen, 8-methoxypsoralen, tri-methoxypsoralen and angelicin. In quantitative terms, the results were in agreement with the values found by others. In kinetic studies using mammalian cells, we found that half of the psoralen-induced ICLs were unhooked within 2.5 h. The rate in normal human diploid fibroblasts was found to be 20,000 ICLs/h/cell. In comparison to survival, 2500 ICLs per cell led to 50% toxicity, indicating that the unhooking of the ICLs is not the crucial step for ICL tolerance. Surprisingly, only 3500 ICLs per cell corresponded to a significant delay in the replication fork elongation. The results indicate involvements of additional pathway(s) for the delay since the effect on replication elongation could be monitored when only 10% of the replication forks encounter an ICL.