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金属硫蛋白基因多态性与2型糖尿病的关系
引用本文:马淑梅,刘晓冬,吕喆,刘淑春,刘扬,姚程.金属硫蛋白基因多态性与2型糖尿病的关系[J].吉林大学学报(医学版),2004,30(2):172-174.
作者姓名:马淑梅  刘晓冬  吕喆  刘淑春  刘扬  姚程
作者单位:1. 吉林大学公共卫生学院流行病学教研室,吉林 长春130021;2. 广西北生药业股份有限公司长春市凯旋制药公司,吉林 长春130052
基金项目:吉林省科技发展计划 , 吉林大学校科研和教改项目
摘    要:目的:探讨金属硫蛋白(metallothionein,MT)基因多态性与中国汉族人群中2型糖尿病(T2DM)发病之间的关系。 方法:采用PCR技术和限制性片段长度多态性(RFLP)的方法检测41名糖尿病患者和53名正常对照者的金属硫蛋白基因家族中的MT4基因(rs666636)201G→A突变,统计各组对象的突变频率。 结果:MT4基因(rs666636)201G→A突变型等位基因(A)频率在糖尿病组和正常对照组中差异有显著性(P<0.05,OR=2.335);AA, GA和GG三种基因型频率分布差异也有显著性 (P<0.05);不同基因型的相对风险分析, GA基因型携带者患2型糖尿病的风险是GG基因型的3.462倍(OR=3.162,95% OR CI=1.389~8.629)。 结论:MT4突变型等位基因与2型糖尿病的发生有显著的关联性,基因突变使2型糖尿病的发病风险增加。

关 键 词:非胰岛素依赖型  金属硫蛋白  多态现象(遗传学)  疾病遗传易感性    
文章编号:1671-587X(2004)02-0172-03
收稿时间:2003-02-25
修稿时间:2003年2月25日

Study on proliferation of hematopoietic cell in patients with myelodysplastic syndrome
MA Shu mei ,LIU Xiao dong ,LU Zhe ,LIU Shu chun ,LIU Yang ,YAO Cheng.Study on proliferation of hematopoietic cell in patients with myelodysplastic syndrome[J].Journal of Jilin University: Med Ed,2004,30(2):172-174.
Authors:MA Shu mei  LIU Xiao dong  LU Zhe  LIU Shu chun  LIU Yang  YAO Cheng
Institution:1. Department of Epidemiology, School of Public Health, Jilin University, Changchun 130021, China;2. Changchun Kaixuan Pharmaceutical Corporation, Guangxi Beisheng PharmaceuticalLtd. Co, Changchun 130052, China
Abstract:ObjectiveTo study the proliferation of hematopoietic cell in patients with myelodysplastic syndrome (MDS). MethodsLiquid single layer culture and semisolid culture in vitro were used and flow cytometry was used to detect the cell cycle, apoptosis and the expressions of PCNA, P53,and BCL 2 Results①The Clony Forming Unit Granulocyte Macroplage(CFU GM) and the Erythroid Clony Forming Unit(CFU E) of myelodysplasyic syndromes (MDS/RA) decreased significantly ( P <0 001); while CFU GM,CFU E of MDS/RAEB could not be detectable; ②The percentage of G1 phase increased and the percentage of S, G 2/M phase decreased significantly ( P <0 01), compared with control group; ③The increase of apoptotic bodies of MDS/RA was much more markedly ( P <0 01), while the changes of those in MDS/RAEB could not be found significantly; the expression of PCNA of MDS increased in both MDS/RA and MDS/RAEB ( P <0 01), especially in MDS/RAEB group;④the protein expression of P53 in MDS increased, while BCL 2 decreased significantly in MDS, compared with normal control ( P <0 01). ConclusionThere are severe abnormalities in hematopoietic cell of patients with MDS, higher proliferation and excessive apoptosis occur in bone marrow cells and the changes of p53,bcl 2 gene suggest their possible participation in the regulation of apoptosis.
Keywords:myelodysplastic syndromes  stem cells  proliferating cell nuclear antigen  cell cycle  apoptosis  protein p53  bcl  2
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