Two New Faces of Amifostine: Protector from DNA Damage in Normal Cells and Inhibitor of DNA Repair in Cancer Cells

0471970 - BFÚ 2020 RIV US eng J - Článek v odborném periodiku
Hofer, Michal - Falk, Martin - Komůrková, Denisa - Falková, Iva - Bačíková, Alena - Klejdus, B. - Pagáčová, Eva - Štefančíková, Lenka - Weiterová, Lenka - Angelis, Karel - Kozubek, Stanislav - Dušek, L. - Galbavy, S.
Two New Faces of Amifostine: Protector from DNA Damage in Normal Cells and Inhibitor of DNA Repair in Cancer Cells.
Journal of Medicinal Chemistry. Roč. 59, č. 7 (2016), s. 3003-3017. ISSN 0022-2623. E-ISSN 1520-4804
Grant CEP: GA ČR GBP302/12/G157; GA ČR(CZ) GA16-12454S; GA MZd NV16-29835A; GA ČR GA16-01137S
Institucionální podpora: RVO:68081707 ; RVO:61389030
Klíčová slova: alternative splicing variant * order chromatin-structure
Obor OECD: Pharmacology and pharmacy; Pharmacology and pharmacy (UEB-Q)
Impakt faktor: 6.259, rok: 2016
Způsob publikování: Omezený přístup
https://pubs.acs.org/doi/10.1021/acs.jmedchem.5b01628#

Amifostine protects normal cells from DNA damage induction by ionizing radiation or chemotherapeutics, whereas cancer cells typically remain uninfluenced. While confirming this phenomenon, we have revealed by comet assay and currently the most sensitive method of DNA double strand break (DSB) quantification (based on gamma H2AX/53BP1 high-resolution immunofluorescence microscopy) that amifostine treatment supports DSB repair in gamma-irradiated normal NHDF fibroblasts but alters it in MCF7 carcinoma cells. These effects follow from the significantly lower activity of alkaline phosphatase measured in MCF7 cells and their supernatants as compared with NHDF fibroblasts. Liquid chromatography-mass spectrometry confirmed that the amifostine conversion to WR-1065 was significantly more intensive in normal NHDF cells than in tumor MCF cells. In conclusion, due to common differences between normal and cancer cells in their abilities to convert amifostine to its active metabolite WR-1065, amifostine may not only protect in multiple ways normal cells from radiation-induced DNA damage but also make cancer cells suffer from DSB repair alteration.
Trvalý link: http://hdl.handle.net/11104/0269330