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OBJECTIVE@#To assess the influence of rs2910164 G/C single nucleotide polymorphism (SNP) of the miR-146a gene on its expression and susceptibility to gastric cancer.@*METHODS@#Fifty three gastric cancer patients and six gastric cancer cell lines were selected for determining the miR-146a expression by Taqman quantitative PCR. A model was constructed to assess the influence of miR-146a overexpression on the growth of AGS gastric cancer cells. A case-control study involving 417 gastric cancer patients and 420 cancer-free individuals was then conducted, and the allelic and genotypic frequencies of the rs2910164 G/C SNP were compared. The genotypes of all subjects were determined by using a Taqman allelic discrimination assay. A Taqman assay was also used to quantify mature and pri-miR-146a transcripts among 65 gastric cancer patients with known genotypes.@*RESULTS@#The expression of miR-146a was down-regulated among the 53 gastric cancer patients and six gastric cancer cell lines. Over-expression of miR-146a has suppressed the growth of gastric cancer by inhibiting the G1/S-phase transition of AGS cells. The case-control study showed that subjects with GC/CC genotypes had significantly lower risk for gastric cancer compared with those with GG genotype. In addition, miR-146a G/C SNP has significantly increased the level of mature miR-146a in those with GC/CC genotype compared with GG genotype.@*CONCLUSION@#Down-regulation of miR-146a may play an important role in the pathogenesis of gastric cancer. The rs2910164 polymorphism of the miR-146a gene may reduce the risk of gastric cancer by influencing the processing of mature miR-146a.
Subject(s)
Humans , Case-Control Studies , Genotype , MicroRNAs/genetics , Polymorphism, Single Nucleotide , Stomach Neoplasms/geneticsABSTRACT
Objective To study the inhalation toxicity of volatile organic compounds in mice. Methods The VOC mixture was prepared according to the monitoring data on indoors air. NIH mices were exposed to the gaseous mixture at the doses of 80.00 mg/m3,64.00 mg/m3,51.28 mg/m3,40.96 mg/m3,32.79 mg/m3 and 26.21 mg/m3 to determine the acute toxicity,and at the doses of 10.75 mg/m3,5.38 mg/m3,2.69 mg/m3 to examine the toxic effect on the weight,organ coefficient,the activity of GSH-Px and SOD and the contents of MDA in the serum. The accumulative toxicity was determined. Results The LD50 of acute inhalation toxicity was 53.74 mg/m3.After exposed to this gaseous mixture for 30 days,the body weight decreased significantly,the organ coefficient of liver and kidney changed,and the activity of GSH-Px and SOD decreased,the contents of MDA in serum increased. The accumulation coefficient was above 5. Conclusion This VOC mixture has weak accumulation toxicity in mice,but have some other toxicity.
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Objective To study the effects of zinc-metallothionein (ZnMT) on the cadmium-induced oxidative damage of liver and kidney in mice. Methods The model of laboratory animal was established by 14 d-cadmium exposure to Kunming mice. Then the cadmium-poisoning mice were grouped as Cd-ZnMT group and Cd-ZnSO4 group and perfused orally by solution of ZnMT and ZnSO4 for 14 days respectively. The morphological changes of liver and kidney were observed by electron microscope. The contents of malonydiadehyde (MDA), the activities of superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px) in supernatant fluid of liver and kidney were determined. Results The decreases of the contents of MDA, the increases of the activities of SOD and GSH-Px in liver and kidney of mice in Cd-ZnMT and Cd-ZnSO4-exposure group were observed compared with those in cadmium-exposure group, the dose-effect relationships were also found. The increases of the activities of SOD and GSH-Px, the decrease of contents of MDA of liver and kidney, were found in Cd-ZnMT-exposure group compared with those of Cd-ZnSO4-exposure group, but without statistical significances. The morphological damages of liver and kidney observed by electron microscope in mice of cadmium-exposure group were more serious than those in mice treated with solution of ZnMT and ZnSO4 after cadmium exposure. Conclusion ZnMT could repair the lipid peroxidative damages in liver and kidney in mice induced by exposure to cadmium in a certain degree.