Title of article :
Elevated Serum 8-Hydroxy-2’-Deoxyguanosine, Nitrite, and Nitrate in Patients with Stage I Multiple Myeloma
Author/Authors :
Khadem Ansari Mohammad-Hassan نويسنده Department of Clinical Biochemistry, School of Medicine, Urmia University of Medical Sciences, Urmia, Iran , Rasmi Yousef نويسنده Department of Biochemistry, Faculty of Medicine, Cellular and Molecular Research Center, Urmia University of Medical Sciences, Urmi, IR Iran , Nozari Samira نويسنده , Faridvand Yousef نويسنده , Asoudeh Mojtaba نويسنده Department of Clinical Biochemistry, Faculty of Medicine, Urmia University of Medical Sciences, Urmia, Iran
Abstract :
[Background]Reactive oxygen species are highly active intermediates, which lead to cellular damage during imbalance between oxidative stress/antioxidant towards oxidative stress. Free radicals have been proposed to have a crucial role in development and progression of human cancer.[Objectives]The main aim of this study was to assess the changes in 8-hydroxy-deoxyguanosine (8-OHdG), nitrite (NO2-), and nitrate (NO3-) levels in patients with Stage I multiple myeloma (MM).[Methods]The serum samples were obtained from 34 patients with stage I MM (22 males and 12 females at stage I) who were matched with healthy control group. Total serum of NO2- and NO3- levels, in addition to serum 8-OHdG levels, were assayed by using the commercial assay kit.[Results]Compared with the healthy case group, the levels of serum NO2- and NO3- (2.54 ± 0.49 vs. 1.75 ± 0.52 µmol/L, P < 0.001 and 6.37 ± 0.94 vs. 2.63 ± 1.06 µmol/L, respectively, P < 0.001) were significantly increased in patients with MM. Higher levels of 8-OHdG in MM patients (157.08 ± 13.61 pg/mL) were observed and compared to the control group (61.48 ± 9.93 pg/mL) and indicated that 8-OHdG levels in patients with cancer were significantly increased than those of the control group (P < 0.001).[Conclusions]Significantly increase in oxidative DNA damage and end-products of nitric oxide (NO) metabolism levels in patients with stage I MM suggest the possible involvement of oxidative stress in MM disease. These alterations can be associated with the imbalance in oxidant-antioxidant status in these patients and may contribute to carcinogenesis of MM by oxidative DNA damage.