1. Inhibitors of poly(ADP-ribose) polymerase enhance unscheduled DNA synthesis in human peripheral lymphocytes
- Author
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Takashi Sugimura, Masanao Miwa, Hiroo Hoshino, Tomoko Kondo, Kazuyuki Ishihara, and Mieko Kanai
- Subjects
DNA Replication ,Xeroderma pigmentosum ,Poly ADP ribose polymerase ,Biophysics ,Poly(ADP-ribose) Polymerase Inhibitors ,Biochemistry ,Structure-Activity Relationship ,chemistry.chemical_compound ,NAD+ Nucleosidase ,medicine ,Humans ,Lymphocytes ,Benzamide ,Molecular Biology ,Polymerase ,biology ,Nicotinamide ,Adenosine diphosphate ribose ,Cell Biology ,medicine.disease ,Molecular biology ,Kinetics ,chemistry ,Unscheduled DNA Synthesis ,Benzamides ,Ultraviolet irradiation ,biology.protein - Abstract
Summary Benzamide and m -aminobenzamide, the most potent inhibitors of poly-(adenosine diphosphate ribose) polymerase known, enhanced unscheduled DNA synthesis after ultraviolet irradiation in human lymphocytes. A positive correlation was found between the inhibitory activities and enhancing effects on unscheduled DNA synthesis of inhibitors related to benzamide and nicotinamide. Lymphocytes of a patient with xeroderma pigmentosum did not show enhanced unscheduled DNA synthesis with these inhibitors after ultraviolet irradiation, but like normal lymphocytes, showed enhanced unscheduled DNA synthesis after treatment with N-methyl-N′-nitro-N-nitrosoguanidine.
- Published
- 1981
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