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   Static magnetic fields modulate X-ray-induced DNA damage in human glioblastoma primary cells  
   
نویسنده teodori l. ,giovanetti a. ,albertini m.c. ,rocchi m. ,perniconi b. ,valente m.g. ,coletti d.
منبع journal of radiation research - 2014 - دوره : 55 - شماره : 2 - صفحه:218 -227
چکیده    Although static magnetic fields (smfs) are used extensively in the occupational and medical fields,few comprehensive studies have investigated their possible genotoxic effect and the findings are controversial. with the advent of magnetic resonance imaging-guided radiation therapy,the potential effects of smfs on ionizing radiation (ir) have become increasingly important. in this study we focused on the genotoxic effect of 80 mt smfs,both alone and in combination with (i.e. preceding or following) x-ray (xr) irradiation,on primary glioblastoma cells in culture. the cells were exposed to: (i) smfs alone; (ii) xrs alone; (iii) xr,with smfs applied during recovery; (iv) smfs both before and after xr irradiation. xr-induced dna damage was analyzed by single cell gel electrophoresis assay (comet assay) using statistical tools designed to assess the tail dna (td) and tail length (tl) as indicators of dna fragmentation. mitochondrial membrane potential,known to be affected by ir,was assessed using the jc-1 mitochondrial probe. our results showed that exposure of cells to 5 gy of xr irradiation alone led to extensive dna damage,which was significantly reduced by post-irradiation exposure to smfs. the xr-induced loss of mitochondrial membrane potential was to a large extent averted by exposure to smfs. these data suggest that smfs modulate dna damage and/or damage repair,possibly through a mechanism that affects mitochondria. © 2013 the author 2013. published by oxford university press on behalf of the japan radiation research society and japanese society for therapeutic radiology and oncology.
کلیدواژه Comet assay; DNA fragmentation; Glioblastoma; Ionizing radiation; Mitochondrial membrane potential; Static magnetic field
آدرس radiation development and application,utaprad-dim,enea,via enrico fermi 45,frascati,rome 00044,italy,fondazione san raffaele,ss ceglie san michele km 1.2,ceglie messapica 72013, Italy, radiation biology and human health utbiorad,enea,via anguillarese 301,casaccia,rome 00123, Italy, institute of biochemistry,university of urbino 'carlo bo',via saffi 2,urbino 61029, Italy, institute of biomathematics,university of urbino 'carlo bo',via saffi 2,urbino 61029, Italy, upmc paris 06,ur4 aging,stress and inflammation,7 quai saint bernard,paris 75252, France, fondazione san raffaele,ss ceglie san michele km 1.2,ceglie messapica 72013, Italy, upmc paris 06,ur4 aging,stress and inflammation,7 quai saint bernard,paris 75252, France
 
     
   
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