Oxidative stress in patients with differentiated thyroid cancer: early effects of radioiodine therapy.

IF 1.5 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Olgica B Vrndic, Snezana D Radivojevic, Marina D Jovanovic, Svetlana M Djukic, Ljiljana C Mijatovic Teodorovic, Snezana T Zivancevic Simonovic
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Abstract

Ionizing radiation in differentiated thyroid cancer (DTC) patients treated with radioiodine (131-I) produces reactive oxygen species (ROS), which could induce oxidative stress with disturbance of redox balance. The aim of this study was to evaluate oxidative stress in DTC patients treated with 3.7 or 5.5 GBq of 131-I using values for serum malondialdehyde (MDA, a marker of oxidative stress), uric acid (to determine antioxidant status) and total antioxidative status (TAS). The study population included 20 DTC patients and 20 healthy controls. Significant differences in MDA concentrations were found between DTC patients before 131-I therapy and control subjects (p = 0.001), while TAS values were similar in both populations (p > 0.05). There was a negative correlation between MDA concentrations and TAS in the DTC group before therapy (R2 = 0.2973, p = 0.013). Three days after 131-I therapy, MDA concentrations were higher than the pretreatment values (3.36 +/- 1.69 nmol/mL vs. 2.93 +/- 1.31 nmol/mL; p = 0.006), while serum uric acid concentrations declined progressively from 341.0 +/- 80.39 micromol/L to 304.25 +/- 77.25 micromol/L (p = 0.026) in 3 days and 291.2 +/- 88.86 micromol/L (p = 0.009) in 7 days after 131-I therapy. There was no dose-dependent effect on MDA, or uric acid concentrations and TAS. Thus, 131-I therapy in DTC patients induced oxidative stress, which was accompanied by a simultaneous and extended reduction in uric acid concentration, but without significant disturbances in TAS. This is the first study that evaluated TAS capacity in DTC patients before and 7 days after 131-I therapy. The relatively stabile TAS values in these patients indicated a good protection from oxidative stress induced by high doses of ionizing radiation.

分化型甲状腺癌患者的氧化应激:放射性碘治疗的早期效果。
放射性碘(131-I)治疗的分化型甲状腺癌(DTC)患者电离辐射产生活性氧(ROS),引起氧化应激并扰乱氧化还原平衡。本研究的目的是评估接受3.7或5.5 GBq 131-I治疗的DTC患者的氧化应激,使用血清丙二醛(MDA,氧化应激的标志物)、尿酸(测定抗氧化状态)和总抗氧化状态(TAS)的值。研究人群包括20名DTC患者和20名健康对照者。DTC患者在131-I治疗前MDA浓度与对照组比较差异有统计学意义(p = 0.001), TAS值在两组比较相似(p > 0.05)。DTC组治疗前MDA浓度与TAS呈负相关(R2 = 0.2973, p = 0.013)。131-I治疗3天后,MDA浓度高于预处理值(3.36 +/- 1.69 nmol/mL vs. 2.93 +/- 1.31 nmol/mL;p = 0.006),而血清尿酸浓度在131-I治疗后3天逐渐从341.0 +/- 80.39微mol/L下降到304.25 +/- 77.25微mol/L (p = 0.026),在7天逐渐下降到291.2 +/- 88.86微mol/L (p = 0.009)。对丙二醛、尿酸浓度和TAS没有剂量依赖性影响。因此,131-I治疗在DTC患者中诱导氧化应激,这伴随着尿酸浓度的同时和延长的降低,但在TAS中没有明显的干扰。这是第一个评估131-I治疗前和治疗后7天DTC患者TAS能力的研究。这些患者相对稳定的TAS值表明对高剂量电离辐射引起的氧化应激具有良好的保护作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Indian journal of biochemistry & biophysics
Indian journal of biochemistry & biophysics 生物-生化与分子生物学
CiteScore
2.90
自引率
50.00%
发文量
88
审稿时长
3 months
期刊介绍: Started in 1964, this journal publishes original research articles in the following areas: structure-function relationships of biomolecules; biomolecular recognition, protein-protein and protein-DNA interactions; gene-cloning, genetic engineering, genome analysis, gene targeting, gene expression, vectors, gene therapy; drug targeting, drug design; molecular basis of genetic diseases; conformational studies, computer simulation, novel DNA structures and their biological implications, protein folding; enzymes structure, catalytic mechanisms, regulation; membrane biochemistry, transport, ion channels, signal transduction, cell-cell communication, glycobiology; receptors, antigen-antibody binding, neurochemistry, ageing, apoptosis, cell cycle control; hormones, growth factors; oncogenes, host-virus interactions, viral assembly and structure; intermediary metabolism, molecular basis of disease processes, vitamins, coenzymes, carrier proteins, toxicology; plant and microbial biochemistry; surface forces, micelles and microemulsions, colloids, electrical phenomena, etc. in biological systems. Solicited peer reviewed articles on contemporary Themes and Methods in Biochemistry and Biophysics form an important feature of IJBB. Review articles on a current topic in the above fields are also considered. They must dwell more on research work done during the last couple of years in the field and authors should integrate their own work with that of others with acumen and authenticity, mere compilation of references by a third party is discouraged. While IJBB strongly promotes innovative novel research works for publication as full length papers, it also considers research data emanating from limited objectives, and extension of ongoing experimental works as ‘Notes’. IJBB follows “Double Blind Review process” where author names, affiliations and other correspondence details are removed to ensure fare evaluation. At the same time, reviewer names are not disclosed to authors.
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