2009
DOI: 10.1111/j.1365-2362.2009.02214.x
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Spontaneous and bleomycin‐induced chromosome damage in non cancer thyroid patients

Abstract: Background Presence of chromosome damage in lymphocytes of patients affected by several diseases, including cancer, was detected by the micronucleus (MN) assay. Individual susceptibility to DNA damage, considered as a risk factor for cancer, can be also evaluated using the bleomycin (BLM) sensitivity test.

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Cited by 9 publications
(5 citation statements)
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“…This possibility is supported by the genotoxicity associated with radiations which were observed by several studies. Such studies have investigated the level of genome damage and micronucleus in thyroid cancer patients environmentally exposed to radiation after the Chernobyl fallout (Sbrana et al 2006 ; Tronko et al 2007 ; Cardis and Hatch 2011 ), after Fukushema in Japan (Medalia 2011 ), in patients affected by thyroid cancer who underwent radiotherapy (Livingston et al 1993 ; Gutierrez et al 1997 , 1999 ; Dardano et al 2007 ; Hooman et al 2008 ), and in people affected by thyroid nodules following occupational exposure to ionizing radiation (Brooks et al 2007 ; Scarpato et al 2009 ).…”
Section: Discussionmentioning
confidence: 99%
“…This possibility is supported by the genotoxicity associated with radiations which were observed by several studies. Such studies have investigated the level of genome damage and micronucleus in thyroid cancer patients environmentally exposed to radiation after the Chernobyl fallout (Sbrana et al 2006 ; Tronko et al 2007 ; Cardis and Hatch 2011 ), after Fukushema in Japan (Medalia 2011 ), in patients affected by thyroid cancer who underwent radiotherapy (Livingston et al 1993 ; Gutierrez et al 1997 , 1999 ; Dardano et al 2007 ; Hooman et al 2008 ), and in people affected by thyroid nodules following occupational exposure to ionizing radiation (Brooks et al 2007 ; Scarpato et al 2009 ).…”
Section: Discussionmentioning
confidence: 99%
“…Some researchers have already successfully employed the ␥-H2AX assay to identify the presence of DSB induced by mutagens or carcinogens in human cell lines (25), to study the progression of a cell tissue from normal to neoplastic (26,27), and to assess the DNA damage in subjects who have undergone diagnostic or radiotherapeutic exposure to ionizing radiation (28 -30). In addition, MN analysis has been used to detect chromosomal anomalies in peripheral lymphocytes of people affected by chronic autoimmune and inflammatory diseases, neurodegenerative disorders, or endocrine-metabolic syndromes (22,(31)(32)(33)(34)(35). Some researchers indicated that a prolonged mitogenic stimulation of T lymphocytes by PHA generated an oxidative burst, inducing a high level of endogenous DSB (36).…”
Section: Discussionmentioning
confidence: 99%
“…We postulate, as supported by other studies, that the overweight/obesity condition, through induced metabolic alteration, mitochondrion malfunctioning, and an altered redox enzyme system, can lead to an imbalance in plasma and intracellular antioxidant/prooxidant activities, predisposing cells to produce an effective increase of reactive oxygen or nitrogen species (5,(52)(53)(54) which, in turn, generates DNA lesions. In this view, two recent studies pointed out that hypothyroid patients, who were nonetheless characterized by an excess of oxidative metabolism, showed more micronucleated lymphocytes than hyperthyroid or euthyroid subjects (22), and cultured in vitro cells supplemented with antioxidants significantly decreased the TNF-␣-induced genetic damage (47). In addition, obese patients may undergo increased levels of basal oxidative metabolism due, for example, to an intrinsic overfunctioning of the intracellular prooxidant apparatus that would lead to an overproduction of free radicals.…”
Section: Discussionmentioning
confidence: 99%
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“…Cytogenetic assay: Cytochalasin B (6 µg/mL; Sigma Aldrich, Milano, Italy) was added at 44 h to all culture tubes to block cell cytokinesis. As described in details elsewhere [30], lymphocytes were harvested at the end of cell culturing by 4 min centrifugation at 2400 rpm, treated with 10 mL of 0.075 mM KC1 for a few min to lyse erythrocytes, prefixed in methanol/acetic acid 3:5, fixed in 100% methanol, washed twice in methanol/acetic acid 7:1, and dropped onto clean glass slides. The air-dried slides were then stained in 5% Giemsa.…”
Section: Human Tumor Cells and Growth Conditionsmentioning
confidence: 99%