2008
DOI: 10.4238/vol7-2gmr441
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Genotoxicity evaluation in chronic renal patients undergoing hemodialysis and peritoneal dialysis, using the micronucleus test

Abstract: ABSTRAcT. Patients with chronic renal disease have an increased incidence of cancer. It is well known that long periods of hemodialysis treatment are linked to DNA damage due to oxidative stress. This genotoxic effect may cause the loss of chromosome fragments, or even entire chromosomes, which form micronuclei after cell division, and can be detected by the micronucleus test. In the present case-control study, we evaluated the genotoxic effect of hemodialysis treatment in 20 patients undergoing hemodialysis, … Show more

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Cited by 32 publications
(31 citation statements)
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“…Collection, staining and analysis of the micronuclei were performed as described else-where (Roth et al, 2008). Briefly, an oral mucosa scraping was carried out to collect exfoliated cells using a wooden, water-soaked tongue depressor.…”
Section: Cell Sampling Slide Preparation and Scoringmentioning
confidence: 99%
“…Collection, staining and analysis of the micronuclei were performed as described else-where (Roth et al, 2008). Briefly, an oral mucosa scraping was carried out to collect exfoliated cells using a wooden, water-soaked tongue depressor.…”
Section: Cell Sampling Slide Preparation and Scoringmentioning
confidence: 99%
“…After finishing the scraping, each tongue depressor was transferred to a centrifuge tube containing phosphate, pH 6.8. Subsequently, they were centrifuged for 10 min and then fixed with methanol:acetic acid (3:1), hydrolysis was done with 1 N HCl at 60°C for 10 min and the coloring of the slides was performed with Schiff-fast-green, according to the methodology described by Roth et al (2008).…”
Section: Methodsmentioning
confidence: 99%
“…After finishing the scraping, each tongue depressor was transferred to a centrifuge tube containing phosphate, pH 6.8. Subsequently, they were centrifuged for 10 min and then fixed with methanol:acetic acid (3:1), hydrolysis was done with 1 N HCl at 60°C for 10 min and the coloring of the slides was performed with Schiff-fastgreen, according to the methodology described by reference number [7].…”
Section: Cytological Preparationsmentioning
confidence: 99%