期刊文献+

抗结核药物肝毒性对血浆miRNA分子表达的影响 被引量:2

Effect of anti-tuberculosis drug-induced hepatotoxicity on plasma microRNA expression
暂未订购
导出
摘要 目的探讨抗结核药物肝毒性(ATDH)对患者血浆中微RNA(miRNA)分子表达的影响。方法对3例活动性肺结核患者用药前和发生ATDH后的血浆标本进行miRNA芯片检测。对存在差异性表达的miRNA分子,采用Real Time-PCR进行验证。应用互联网miRNA靶基因预测软件对经证实存在差异性表达的miRNA进行靶基因预测,采用PANTHER蛋白分类系统查找靶蛋白基因本体(GO)功能分类。结果 ATDH发生后,血浆中共筛选出22个与用药前比较差异性表达的miRNA分子,表达上调和下调的miRNA各11个。Real Time-PCR验证结果显示:ATDH发生后,患者血浆中显著上调的miRNA有5个,分别为miR-378i、miR-125b-5p、miR-1224-5p、miR-194-5p和miR-34a-5p;下调的miRNA有3个,分别为miR-1260a、miR-338-3p和miR-4286。结论 ATDH发生患者血浆中存在与用药前比较差异性表达的miRNA分子,这些分子的存在可能与ATDH的发生有关。 Objective To investigate the effect of anti-tuberculosis drug-induced hepatotoxicity (ATDH) on the expression of miRNA in patients' plasma. Methods The plasma from 3 patients with ATDH was collected and subjected to miRNA microarray analysis before anti-tuberculosis treatment and after liver injury during drug therapy. The differentially expressed miRNAs were verified using real-time quantitative PCR. The target genes of miRNAs were predicted by the Internet software, and the GO functional classification of target proteins were found by the PANTHER protein classification system. Results After ATDH had occurred, the microarray screened 22 differentially expressed miRNAs compared to those of pretreatment, among which II were up-regulated, and 11 were down-regulated. Real-time quantitative PCR results showed that after ATDH there were 5 up-regulated miRNAs, namely miR-378i, miR-125b-Sp, miR-1224-Sp, miR-194-Sp and miR-34a-Sp, and 3 down-regulated miRNAs, namely miR-1260a, miR-338-3p and miR-4286. Conclusion There are differentially expressed miRNAs in the plasma of patients after ATDH, and these miRNAs may be related to the incidence of ATDH.
出处 《上海交通大学学报(医学版)》 CAS CSCD 北大核心 2014年第2期154-160,164,共8页 Journal of Shanghai Jiao tong University:Medical Science
基金 国家自然科学基金(81070357 30660066) 上海市松江区医学领先合作项目(2011LX02)~~
关键词 抗结核药物 肝毒性 微RNA 血浆 差异性表达 anti-tuberculosis drug hepatotoxicity microRNA plasma differentially expressed
  • 相关文献

参考文献1

共引文献2917

同被引文献24

  • 1俞焙秦,刘炳亚.miRNA的生物学特性和功能[J].上海交通大学学报(医学版),2007,27(5):621-623. 被引量:31
  • 2Chen YH, Heneidi S, Lee JM, et al. miRNA-93 inhibits GLUT4 and is overexpressed in adipose tissue of polycystic ovary syndrome patients and women with insulin resistance[ J]. Diabetes, 2013, 62 (7) : 2278 -2286.
  • 3Long J, Wang Y, Wang W, et al. Identification of microRNA-93 as a novel regulator of vascular endothelial growth factor in hyperglyce- mic conditions[J]. J Biol Chem, 2010, 285(30) : 23457 -2365.
  • 4Fabbri E, Borgatti M, Montagner G, et al. Expression of micmRNA-93 and Interleukin-8 during Pseudomonas aeruginosa-mediated indue- tion of proinflammatory responses[ J]. Am J Respir Cell Mol Biol, 2014, 50(6) : 1144 -1155.
  • 5McCallie BR, Parks JC, Strieby AL, et al. Human blastocysts exhibit unique microRNA profiles in relation to maternal age and chromosome constitution[J]. J Assist Reprod Genet, 2014, 31 (7) : 913 -919.
  • 6Coordes A, Lenarz M, Kaufmann AM, et al. Role of miRNA in malignoma of the head and neck [ J]. Laryngorhinootologie, 2014, 93(3) : 201 -219.
  • 7Wu Y, Zuo J, Zhang Y, et al. Identification of miR-106b-93 as a negative regulator of brown adipocyte differentiation [ J ]. Biochem Biophys Res Commun, 2013, 438(4) : 575 -580.
  • 8Salas-Perez F, Codner E, Valencia E, et al. MicroRNAs miR-21a and miR-93 are down regulated in peripheral blood mononuclear ceils (PBMCs) from patients with type 1 diabetes[J]. Immunobidogy, 2013, 218(5): 733-737.
  • 9Cavari Y, Landau D, Sorer S, et al. Organophosphate poisoning- induced acute renal failure [ J]. Pediatr Emerg Care, 2013, 29 (5) : 646 - 647.
  • 10赵树靓,房静远.miRNA与肿瘤——表观遗传学新进展[J].上海交通大学学报(医学版),2008,28(12):1584-1586. 被引量:4

引证文献2

二级引证文献11

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