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人脑胶质瘤中Smad-1、Smad-2和Smad-4的表达及意义
引用本文:陈彩霞,蔡 军,魏晓霞,邹 杰,鲍玉洲,步星耀.人脑胶质瘤中Smad-1、Smad-2和Smad-4的表达及意义[J].肿瘤防治研究,2014,41(1):22-26.
作者姓名:陈彩霞  蔡 军  魏晓霞  邹 杰  鲍玉洲  步星耀
作者单位:1.450003郑州,河南省人民医院检验科,2.眼科研究所,3.神经外科三
基金项目:河南省科技创新杰出人才计划项目资助课题(084200410011)
摘    要:目的 检测BMPs/BMPR/Smads信号转导通路上的人脑胶质瘤组织中Smad-1、Smad-2、Smad-4的表达,探讨其在人脑胶质瘤发生发展中的作用及其与临床病理分级的关系。方法 分别应用RT-PCR技术和免疫组织化学SABC法检测20例正常脑组织和40例不同级别人脑胶质瘤组织中Smad-1、Smad-2、Smad-4 mRNA和蛋白质表达量,并分析其与患者的年龄、性别、病理分级的相关性。结果 人脑胶质瘤组织Smad-1、Smad-2、Smad-4 mRNA表达量比正常脑组织显著降低(0.277±0.125 vs.0.573±0.097,P<0.01;0.282±0.111 vs. 0.613±0.105,P<0.01;0.389±0.101 vs. 0.483±0.098,P<0.05),且Ⅲ+Ⅳ组显著低于Ⅰ+Ⅱ组(0.250±0.106 vs. 0.327±0.119,P<0.05;0.2451±0.109 vs. 0.315±0.113,P<0.05;0.347±0.121 vs. 0.434±0.102,P<0.05)。蛋白质表达的阳性率显著低于正常脑组织(37.50%vs. 75.00%,P<0.0 1;20.00% vs. 65.00%,P<0.01; 25.00% vs. 70.00%,P<0.01),且Ⅲ+Ⅳ组显著低于Ⅰ+Ⅱ组(16.67% vs. 54.55%,P<0.05;5.56% vs. 31.82%, P<0.05;5.56% vs. 40.91%,P<0.05)。上述指标的变化与患者的年龄及性别无关。结论 Smad-1、Smad-2、Smad-4 在人脑胶质瘤中的表达水平与胶质瘤的发生发展和恶性程度密切相关,提示Smad-1、Smad-2、Smad-4可能参与胶质瘤发生发展过程。

关 键 词:脑胶质瘤  Smads  信号转导通路  反转录-聚合酶链式反应  免疫组织化学  
收稿时间:2012-10-15

Expression and Signifi cance of Smad-1, Smad-2 and Smad-4 in Human Glioma
CHEN Caixia,CAI Jun,WEI Xiaoxia,ZOU Jie,BAO Yuzhou,BU Xingyao.Expression and Signifi cance of Smad-1, Smad-2 and Smad-4 in Human Glioma[J].Cancer Research on Prevention and Treatment,2014,41(1):22-26.
Authors:CHEN Caixia  CAI Jun  WEI Xiaoxia  ZOU Jie  BAO Yuzhou  BU Xingyao
Institution:1.Clinical Laboratory,He'nan Province People's Hospital, Zhengzhou 450003,China,2. Ophthalmological Research Institute,3.Three Department of Neurosurgery
Abstract:Objective To detect the expressions of Smad-1,Smad-2 and Smad-4 of BMPs/BMPR/Smadssignaling transduction pathway in human brain glioma, to research their role of them in tumorigenesis andprogression of brain glioma and their correlation with clinical pathology. Methods The mRNA and proteinexpressions of Smad-1,Smad-2 and Smad-4 were detected in 20 normal brain tissues and 40 sampleswith human glioma by RT-PCR and SABC immunohistochemical methods, respectively, and analyzed thecorrelation with the patient's age, gender and pathological grade. Results Compared with normal braintissues, Smad-1,Smad-2 and Smad-4 mRNA expressions in human glioma were reduced signifi cantly(0.277±0.125 vs. 0.573±0.097, P<0.01;0.282±0.111 vs. 0.613±0.105, P<0.01;0.389±0.101 vs. 0.483±0.098,P<0.05 )especially in Ⅲ and Ⅳ stage tumor tissues(0.250±0.106 vs. 0.327±0.119,P<0.05;0.2451±0.109 vs. 0.315±0.113,P<0.05;0.347±0.121 vs. 0.434±0.102,P<0.05),and protein expressionsin human glioma were reduced significantly(37.50% vs. 75.00% , P<0.0 1;20.00% vs. 65.00%,P<0.01;25.00% vs. 70.00%,P<0.01)especially in Ⅲ and Ⅳ stage tumor tissues(16.67% vs. 54.55%,P<0.05;5.56% vs. 31.82%,P<0.05;5.56% vs. 40.91%,P<0.05). The difference was not related withthe patient’s age and gender. Conclusion Expressions of Smad-1,Smad-2 and Smad-4 in human gliomaare closely related with glioma malignant degree. It prompts Smad-1, Smad-2 and Smad-4 participate in brainglioma occurrence and development process.
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