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肾脏纤维化大鼠模型尿液中差异表达基因筛选及生物信息学分析 被引量:2

Differentially expressed gene screening of urine samples from rats renal fibrosis model and bioinformatics analysis
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摘要 目的研究大鼠肾脏纤维化(RF)模型尿液中差异表达的基因,并对其进行生物信息学分析。方法将大鼠分为对照组和纤维化模型组,单侧输尿管结扎术建立大鼠肾脏纤维化模型,收集尿液。提取总RNA,构建测序文库并进行转录组测序。对差异表达的mRNA进行了GO分析和KEGG分析,并对miRNA的前体和lncRNA的家族进行预测和分类。结果肾脏纤维化模型组的尿液和对照组相比,得到813条表达上调转录本数据以及213条表达下调的转录本数据。结论利用转录组高通量测序结合相关生物信息学分析,可为肾脏纤维化诊断靶点提供新的可能。 Objective To investigate the differentially expressed genes of urine samples from renal fibrosis model and carry out bioinformatics analysis. Methods Rat renal fibrosis model was constructed with the method of unilateral ureteric obstruction. Urine were collected from the rats with unilateral obstructive nephropathy and sham group,respectively. Total RNA was extracted and sequencing library was established. Differential expression mRNA were analyzed by GO and KEGG pathway. Known pre-miRNA were detected and novel lncRNA family were classified.Results Compared with the sham group urine,813 up-regulated mRNA/lncRNA and 213 down-regulated mRNA/lncRNA were collected from the urine of renal fibrosis rats. Conclusions There are significant differential expression profile in urine samples between renal fibrosis rat group and the shame group. With high-throughput transcriptome sequencing and bioinformatics analysis,the exciting possibility was raised for better understanding renal pathologies and development of new diagnostic biomarkers.
出处 《基础医学与临床》 CSCD 2017年第4期500-505,共6页 Basic and Clinical Medicine
基金 国家重点基础研究发展计划(2013CB530800)
关键词 肾脏纤维化 生物信息学分析 转录组测序 单侧输尿管结扎 renal fibrosis bioinformatics analysis transcriptome sequencing unilateral ureteric obstruction
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  • 1Ferlay J, Parkin DM, Steliarova-Foucher E. Estimates of cancer incidence and mortality in Europe in 2008. Eur J Cancer 2010; 46: 765-81.
  • 2Siegel R, Naishadham D, Jemal A. Cancer statistics, 2012. CA Cancer J Clin 2012; 62: 10-29.
  • 3Roddam AW, Duffy MJ, Hamdy FC, Ward AM, Patnick Jet al. Use of prostate-specific antigen (PSA) isoforms for the detection of prostate cancer in men with a PSA level of 2-10 ng/ml: systematic review and meta-analysis. Eur Urol 2005; 48: 386-99; discussion 98-9.
  • 4Li S, Hursting SD, Davis BJ, McLachlan JA, Barrett JC. Environmental exposure, DNA methylation, and gene regulation: lessons from diethylstilbesterol-induced cancers. Ann N YAcad Sci 2003; 983: 161-9.
  • 5Jones PA, Baylin SB. The fundamental role of epigenetic events in cancer. Nat Rev Genet 2002; 3: 415-28.
  • 6Goessl C, Krause H, Muller M, Heicappell R, Schrader M et al. Fluorescent methylation-specific polymerase chain reaction for DNA-based detection of prostate cancer in bodily fluids. Cancer Res 2000; 60: 5941-5.
  • 7Nakayama M, Bennett CJ, Hicks JL, Epstein J I, Platz EA et al. Hypermethylation of the human glutathione S-transferase-pi gene (GSTP1) CpG island is present in a subset of proliferative inflammatory atrophy lesions but not in normal or hyperplastic epithelium of the prostate: a detailed study using laser-capture microdissection. Am J Pathol 2003; 163:923-33.
  • 8Lee WH, Morton RA, Epstein JI, BrooksJD, Campbell PA et al. Cytidine methylation of regulatory sequences near the pi-class glutathione S-transferase gene accompanies human prostatic carcinogenesis. Proc Natl Acad Sci USA 1994; 91: 11733-7.
  • 9Goessl C, Muller M, Heicappell R, Krause H, Straub B et al. DNA-based detection of prostate cancer in urine after prostatic massage. Urology 200 1; 58: 335-8.
  • 10Woodson K, O'Reilly KJ, Hanson JC, Nelson D, Walk EL et al. The usefulness of the detection of GSTP1 methylation in urine as a biomarker in the diagnosis of prostate cancer. Urol 2008; 179: 508-11; discussion 11-2.

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