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荧光定量分析人皮肤瘢痕疙瘩组织中miRNA-34s的表达
引用本文:金玉丹,郭晓瑞,黄海华,卢玲,蔡小健,王绥江.荧光定量分析人皮肤瘢痕疙瘩组织中miRNA-34s的表达[J].中国临床康复,2014(11):1694-1699.
作者姓名:金玉丹  郭晓瑞  黄海华  卢玲  蔡小健  王绥江
作者单位:[1] 中山市第二人民医院激光美容整形中心,广东省中山市,528447 [2] 广东医学院附属医院整形外科研究所,广东省湛江市,524001 [3] 赣南医学院第一附属医院整形外科,江西省赣州市,341000
基金项目:中山市科技计划项目(20122A041)资助
摘    要:背景:通过分析不同肿瘤组织与正常组织miRNA表达谱的差异,有可能筛选到特异性好、灵敏度高、可作为特定肿瘤分子标志物的miRNA。目的:采用实时荧光定量RT-PCR检测miRNA-34家族(miRNA-34s:miR-34a/b/c)在瘢痕疙瘩和正常皮肤组织中的差异表达,分析评价microRNA-34s在瘢痕疙瘩形成发展的作用及可能的机制影响。方法:收集手术切除瘢痕疙瘩组织(10例)和正常皮肤(2例);TRIZOL法提取标本的总RNAs并进行质检,再采用 Ambion′s miRNA Isolation Kit 从总 RNAs 中分离 microRNA,采用实时荧光定量 RT-PCR 技术检测miRNA-34s(miR-34a/b/c)在瘢痕疙瘩组织和正常皮肤组织中的表达水平。结果与结论:miRNA-34s(miRNA-34a/b/c)在瘢痕疙瘩组织中均呈下调表达(P<0.01)。表明该家族成员参与了瘢痕疙瘩的形成发展,下调表达的miRNA-34s可能导致了瘢痕疙瘩的肿瘤性生长。

关 键 词:组织构建  组织工程  瘢痕疙瘩

Fluorescent quantitative analysis on the expression of miRNA-34s in human skin keloid tissue
Jin Yu-dan,Guo Xiao-rui,Huang Hai-hua,Lu Ling,Cai Xiao-jian,Wang Sui-jiang.Fluorescent quantitative analysis on the expression of miRNA-34s in human skin keloid tissue[J].Chinese Journal of Clinical Rehabilitation,2014(11):1694-1699.
Authors:Jin Yu-dan  Guo Xiao-rui  Huang Hai-hua  Lu Ling  Cai Xiao-jian  Wang Sui-jiang
Institution:1Cosmetic Surgery & Laser Center, Second People's Hospital of Zhongshan City, Zhongshan 528447, Guangdong Province, China; 2Plastic Surgery Institute, Affiliated Hospital of Guangdong Medical College, Zhanjiang 524001, Guangdong Province, China; 3Department of Plastic Surgery, First Affiliated Hospital of Gannan Medical College, Ganzhou 341000, Jiangxi Province, China)
Abstract:BACKGROUND:Understanding the difference of miRNA-34s expression in normal tissue and tumor tissue wil contribute to screen out a miRNA with high sensitivity as the specific tumor molecular marker.OBJECTIVE:To investigate the differential expression of miRNA-34s (miR-34a/b/c) between normal skin and keloid tissue using real-time fluorescent quantitative PCR, and to evaluate the role and mechanisms of miRNA-34s in keloid formation and development.METHODS:Ten cases of keloid tissue and two cases of normal skin tissue were col ected as specimens. Total RNAs were extracted from keloid and nomal skin tissue by Trizol method, and miRNA-34s were further isolated by Ambion’s miRNA Isolation Kit. Real-time fluorescent quantitative PCR was applied to verify expression levels of microRNA-34s (miR-34a/b/c) in keloid tissue and normal skin tissue.RESULTS AND CONCLUSION:miRNA-34s (miRNA-34a/b/c) expression was down-regulated in keloid tissue compared with normal skin tissue (P〈0.01). The findings showed that miRNA-34s (miRNA-34a/b/c) are involved in keloid formation and development, and down-regulation of the family member may result in neoplastic growth of keloid.
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