期刊文献+

炎性肿块肺纤维化组织中miR-21和TGFβ1的表达变化 被引量:3

Expression of MiR-21 and TGFβl in Pulmonary Fibrosis of Inflammatory Mass and Its Signifi-cance
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摘要 【目的】观察炎性肿块肺纤维化组织中miR-21和转化生长因子B1(transforminggrowthfactor171,TGFβ1)的表达变化,探讨两者的表达变化是否与肺纤维化形成有关。【方法】选择10例炎性肺部肿块标本,每例分别按纤维化组织和旁近正常肺组织配对留取,所有标本均采用Real-timePCR方法检测组织中miR-21和TGFβ1的表达量变化,分析其表达是否与肺纤维化有关。【结果】肺纤维化组织中miR-21和TGFβ1的表达明显高于正常旁近肺组织,且两者相比较差异均有显著性(P〈0.01)。【结论1miR-21和TGFβ1在炎性肿块肺纤维化组织中高表达,其高表达与炎症导致的肺纤维化形成有关。 [Objective]To examine the levels of expression of microRNA-21 (miR-21) and transforming growth factorβ1 (TGF-β1)in lung tissues with fibrosis and its adjacent non fibrosis tissues.[Methods]Specimens of pulmonary fibrosis tissue and adjacent tissues were collected from 10 patients. Their miR-21 and TGFβ1 expression levels were detected by Real-time PCR. [Results]High sensitivity, specificity, and precision of RT-PCR allowed for direct analy- sis of expression of miR-21 and TGFβ1 expression in pulmonary fibrosis tissues and adjacent tissues. The expression miR-21 and TGFβ1 in pulmonary tissues was significantly higher than in adjacent tissues ( P〈0.001). [Conclusions] Elevated expression of miR-21 and TGFβ1 play an important role in the pathogenesis of diseases related to fibro-genic reactions in pulmonary inflammatory mass patients.
出处 《医学临床研究》 CAS 2016年第5期856-858,共3页 Journal of Clinical Research
基金 湖南省科技厅项目(编号:2013FJ3126) 湖南省肿瘤医院青年基金项目(编号:B2012-03)
关键词 肺纤维化 肺炎 微RNAS 转化生长因子Β1 Pulmonary Fibrosis Pneumonia MicroRNAs Transforming Growth Factor betal
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参考文献14

  • 1Cutroneo KR, White SL, Phan SH, et al .Therapies for bleo- mycin induced pulmonary fibrosis through regulation of TGF- betal induced collagen gene expression[J]. J Cell Physiol, 2007,211(3) :585-589.
  • 2Uhal BD, Kim JK, Li X, et al . Angiotensin TGFI31 crosstalk in human idiopathic pulmonary fibrosis: autocrine mecha- nisms in myofibroblasts and macrophages[J]. Curr Pharm Des, 2007,13(12) :1247-1256.
  • 3Wynn TA. Cellular and molecular mechanisms of fibrosis[J]. J Pathol, 2008,214(2) : 199 210.
  • 4Wynn TA. Common and unique mechanisms regulate fibrosis in various fibroproliferative diseases[J]. J Clin Invest, 2007, 117(3) : 524-529.
  • 5Zimmer V, Lammert F. Genetics in liver disease: new con- cepts[J]. Curr Opin Gastroenterol, 2011, 27(3) : 231 -239.
  • 6Dussaule JC, Guerrot D, Huby AC, et al . The role of cell plasticity in progression and reversal of renal fibrosis[J], lnt J Exp Pathol, 2011,92(3): 151-157.
  • 7Griffiths-Jones S, Saini HK, van Dongen S, et al . miRBase: tools for microRNA genomies[J]. Nucleic Acids Res, 2008, 36(Database issue) :D154 -158.
  • 8Lewis BP, Burge CB, Bartel DP. Conserved seed pairing, of- ten flanked by adenosines, indicates that thousands of human genes are microRNA targets[J]. Cell, 2005,120(1):15-20.
  • 9葛燕,陈国纯,孙林,刘伏友.MicroRNA-29与纤维化疾病[J].中南大学学报(医学版),2011,36(9):908-912. 被引量:10
  • 10Kang HY. MicroRNA 21 regulates stemness in cancer cells [J]. Stem Cell Res Ther, 2013,4(5) : 110-113.

二级参考文献26

  • 1Lagos-Quintana M,Rauhut R,Lendeckel W,et al.Identification of novel genes coding for small expressed RNAs[J].Science,2001,294(5543):853-858.
  • 2Hwang H W,Wentzel E A,Mendell J T.A hexanucleotide element directs microRNA nuclear import[J]. Science,2007,315(5808):97-100.
  • 3Feldman A L,Dogan A,Smith D I,et al.Discovery of reeurrent t (6 ; 7) (p25.3 ; q32.3) translocations in ALK-negative anaplastic large cell lymphomas by massively parallel genomic sequencing[J].Blood,117(3):915-919.
  • 4Long J,Wang Y,Wang W,et al.MicroRNA-29c is a signature MicroRNA under high glucose conditions which targets sprouty homolog 1,and its in vivo knockdown prevents progression of diabetic nephropathy[J].J Biol Chem,2011,286 (13):11837-11848.
  • 5Forman J J,Legesse-Miller A,Coller H A.A search for conserved sequences in coding regions reveals that the let-7 microRNA targets Dicer within its coding sequence[J].Proc Natl Acad Sci USA,2008,105(39):14879-14884.
  • 6Ott C E,Grunhagen J,Jager M,et al.MicroRNAs differentially expressed in postnatal aortic development downregulate elastin via 3′ UTR and coding-sequence binding sites[J].PLoS One,2011,6(1):e16250.
  • 7Bartel D P.MicroRNAs:target recognition and regulatory functions[J].Cell,2009,136(2):215-233.
  • 8Li Z,Hassan M Q,Jafferji M,et al.Biological functions of miR-29b contribute to positive regulation of osteoblast differentiation[J].J Biol Chem,2009,284(23):15676-15684.
  • 9Bettens K,Brouwers N,Engelborghs S,et al. APP and BACE1 miRNA genetic variability has no major role in risk for Alzheimer disease[J].Hum Mutat,2009,30 (8):1207-1213.
  • 10Xu H,Cheung I Y,Guo H F,et al.MicroRNA miR-29 modulates expression of immunoinhibitory molecule B7-H3:potential implications for immune based therapy of human solid tumors[J].Cancer Res,2009,69(15):6275-6281.

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