期刊文献+

寻常型银屑病患者皮损中miRNA-34a及其靶基因Notch1的表达及意义 被引量:4

Expression and Significance of mi RNA-34a and its Target Gene Notch1 in Lesions of Patients with Psoriasis Vulgaris
下载PDF
导出
摘要 目的:探讨miRNA-34a及其靶基因Notch1在寻常型银屑病患者皮损中的表达水平及意义。方法:实时荧光定量PCR法检测22例寻常型银屑病患者皮损组织及10例正常人皮肤组织中miRNA-34a的表达水平。采用免疫组化EnVision法检测51例寻常型银屑病患者(包括上述22例患者)和29例正常人(包括上述10例正常人)皮损组织中miRNA-34a可能的靶基因Notch1的表达情况。结果:miRNA-34a在寻常型银屑病患者皮损组织中的表达水平为0.162±0.186,高于正常皮肤组织中的表达水平(0.028±0.029),银屑病组为正常对照组的5.786倍,两组比较,差异有统计学意义(t=2.22,P〈0.05);Notch1在寻常型银屑病组织中主要为表皮全层细胞质表达,阳性表达率为76.47%(39/51),而在正常皮肤组织中阳性表达率为13.79%(4/29),两者差异有统计学意义(χ^2=29.22,P〈0.05)。结论:miRNA-34a在寻常型银屑病皮损组织中的表达高于正常人皮肤组织,其可能通过调控靶基因Notch1参与寻常型银屑病的发病机制。 Objective: To investigate the expression and significance of miRNA-34 a and its target gene Notch1 in lesions of patients with psoriasis vulgaris. Methods: Real-time fluorescent quantitative PCR was performed to determine the expression level of miRNA-34 a in 22 patients with psoriasis vulgaris and normal skin of 10 healthy human controls. Potential target genes of mi RNA-34 a were found using software of mi Rwalk to predict target gene,then the expression of Notch1 was detected by immunohistochemistry in 51 patients with psoriasis vulgaris( including 22 patients above) and 29 healthy controls( including 10 healthy people above). Results: Real-time fluorescent quantitative PCR showed that the expression level of miRNA-34 a was higher in lesions of psoriasis vulgaris than that in the normal skin [( 0. 162 ± 0. 186) vs( 0. 028 ± 0. 029),times:5. 786,t = 2. 22,P〈0. 05]. The Notch1 was expressed in epidermal cytoplasm at full-thickness of epidermis in lesions of psoriasis vulgaris and the positive rate was 76. 47%( 39 /51),while the positive rate was 13. 79%( 4 /29) in normal skin. There was statistical significance between the two groups( χ^2= 29. 22,P〈0. 05). Conclusion: The expression level of mi RNA-34 a was significantly up-regulated in lesions of psoriasis vulgaris,which might be regulated its target genes Notch1 and played a part in the pathogenesis of psoriasis vulgaris.
出处 《皮肤性病诊疗学杂志》 2015年第6期423-427,共5页 Journal of Diagnosis and Therapy on Dermato-venereology
基金 新疆维吾尔自治区自然科学基金(编号:2015211C201)
关键词 银屑病 寻常型 miRNA-34a 靶基因 NOTCH1 Psoriasis Vulgaris MiRNA-34a Target genes Notch1
  • 相关文献

参考文献12

  • 1Ota T,Takekoshi S,Takagi T,et al.Notch signaling may be involved in the abnormal differentiation of epidermal keratinocytes in psoriasis[J].Acta Histochem Cytochem,2014,47(4):175-183.
  • 2Guruharsha KG,Kankel MW,Artavanis-Tsakonas S.The Notch signalling system:recent insights into the complexity of a conserved pathway[J].Nat Rev Genet,2012,13(9):654-666.
  • 3孙中斌,晋亮,党二乐,郭森,李春英,王刚.MiR-486-3p在银屑病皮损的表达及对角蛋白17表达的影响[J].中华皮肤科杂志,2013,46(3):160-163. 被引量:6
  • 4Zhao M,Wang LT,Liang GP,et al.Up-regulation of micro RNA-210 induces immune dysfunction via targeting FOXP3 in CD4(+)T cells of psoriasis vulgaris[J].Clin Immunol,2014,150(1):22-30.
  • 5Xu N,Meisgen F,Butler LM,et al.Micro RNA-31 is overexpressed in psoriasis and modulates inflammatory cytokine and chemokine production in keratinocytes via targeting serine/threonine kinase 40[J].J Immunol,2013,190(2):678-688.
  • 6娄文加,陈青,刘立,钱程.miR-34家族——肿瘤抑制蛋白p53高度相关的microRNA[J].遗传,2010,32(5):423-430. 被引量:16
  • 7He L,He X,Lim LP,et al.A micro RNA component of the p53 tumour suppressor network[J].Nature,2007,447(7148):1130-1134.
  • 8崔红宙,张开明,王丽.银屑病p53通路表观遗传机制的研究动态[J].中国中西医结合皮肤性病学杂志,2010,9(6):395-397. 被引量:6
  • 9Blanpain C,Lowry WE,Pasolli HA,et al.Canonical notch signaling functions as a commitment switch in the epidermal lineage[J].Genes Dev,2006,20(21):3022-3035.
  • 10Abdou AG,Maraee AH,Sharaf A,et al.Up-regulation of Notch-1 in psoriasis:an immunohistochemical study[J].Ann Diagn Pathol,2012,16(3):177-184.

二级参考文献99

共引文献29

同被引文献43

  • 1王海晶,杨和平.姜黄挥发油对人肺腺癌A549细胞作用的形态学研究[J].第三军医大学学报,2005,27(3):220-222. 被引量:14
  • 2曹冬梅,卢建.叉头框(Fox)转录因子家族的结构与功能[J].生命科学,2006,18(5):491-496. 被引量:35
  • 3江从军,刘贞富,徐秋梅,马利娟,余慧敏.生存素在寻常型银屑病皮损中的表达[J].中国麻风皮肤病杂志,2007,23(5):391-392. 被引量:7
  • 4Ying SY. Micro RNA protocols [M]. Humana Press Inc, 2008:1-13.
  • 5Pellegrino L, Jacob J, Roca-Alonso L, et al. Altered expression of the miRNA processing endoribonuclease Dicer has prognostic significance in human cancers [J]. Expert Rev Anticancer Ther, 2013, 13:21-27.
  • 6Pereira DM, Rodrigues PM, Borralho PM, et al. Delivering the promise of miRNA cancer therapeutics [J]. Drug Discov Today, 2013, 18:282-289.
  • 7Asrih M, Steffens S. Emerging role of epigenetics and miRNA in diabetic cardiomyopathy [J]. Cardiovasc Pathol, 2013, 22:117-125.
  • 8Akbari Moqadam F, Pieters R, den Boer ML. The hunting of targets: challenge in miRNA research [J]. Leukemia, 2013, 27: 16-23.
  • 9Ishida M, Selaru FM. miRNA-Based Therapeutic Strategies [J]. Curr Anesthesiol Pep, 2013, 1: 63-65.
  • 10Cheung L, Fisher RM, Kuzmina N, et al. Psoriasis Skin Inflammation-Induced microRNA-26b Targets NCEH1 in Underlying Subcutaneous Adipose Tissue [J]. J Invest Dermatol, 2016, 136(3):640-648.

引证文献4

二级引证文献13

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部