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miR-143在胰腺癌组织中的表达及临床意义 被引量:5

Clinical significance of expression of miR-143 in pancreatic carcinoma
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摘要 目的:探究miR-143在胰腺导管腺癌(pancreatic ductal adenocarcinoma,PDAC)组织中的表达与临床参数、预后的相关性.方法:收集70例PDAC患者的癌组织及配对癌旁组织石蜡切片,应用锁定核酸原位杂交(locked nucleic acids-in situ hybridization,LNA-ISH)法检测组织中miR-143的表达水平,收集相关临床资料,并对患者的预后进行随访,采用SPSS16.0进行统计学分析.结果:PDAC癌组织中miR-143阳性表达率明显低于癌旁组织(25.71%vs 68.57%,P=0.001),miR-143的表达与淋巴结转移相关,差异有统计学意义(P=0.045).生存分析结果显示,mi R-143阳性者的预后较好(P=0.026).结论:PDAC患者癌组织中mi R-143呈低表达,且与不良预后相关. AIM: To investigate the expression of mi R-143in human pancreatic ductal adenocarcinoma(PDAC) and to explore the relation between mi RNA-143 expression and prognosis of patients with PDAC. METHODS: We collected 70 PDAC specimens from patients treated at the First Affiliated Hospital of Zhengzhou University, including cancer tissues and paired cancer-adjacent tissues. The expression of miR-143 was examined by locked nucleic acids-in situ hybridization(LNAISH). Then the relation between the expression of miR-143 and clinical parameters was analyzed with SPSS16.0. RESULTS: The expression rate of miR-143 was lower in cancerous tissues than in paired non-cancerous pancreatic tissues(25.71% v s 68.57%, P=0.001). The expression of miR-143 in cancerous tissues was associated with lymph node metastasis(P = 0.045). The median survival of patients with low mi R-143 expression was significantly shorter than that of patients with high miR-143 expression(P = 0.026). CONCLUSION: The expression of miR143 is low in cancer tissue, and its low expression is associated with poor prognosis in patients with PDAC.
出处 《世界华人消化杂志》 CAS 2016年第10期1520-1525,共6页 World Chinese Journal of Digestology
关键词 胰腺癌 MIR-143 锁定核酸原位杂交 预后 Pancreatic cancer miR-143 Locked nucleic acids-in situ hybridization Prognosis
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  • 1Zamore PD,Haley B.Ribo-genome:the big world of small RNAs[J].Science,2005,309(5740):1519-1524.
  • 2Lagos-Quintana M,Rauhut R,Yalcin A,et al.Identification of tissue-specific microRNAs from mouse[J].Curr Biol,2002,12(9):735-739.
  • 3Hobert O.Gene regulation by transcription factors and microRNAs[J].Science,2008,319(5871):1785-1786.
  • 4Martinez NJ,Ow MC,Barrasa MI,et al.A C.elegans genome-scale microRNA network contains composite feedback motifs with high flux capacity[J].Genes Dev,2008,22(18):2535-2549.
  • 5Rasmussen KD,Simmini S.Abreu-Goodger C,et al.The miR-144/451 locus is required for erythroid homeostasis[J].J Exp Med,2010,207(7):1351-1358.
  • 6Fabbri M,Croce CM,Calin GA.MicroRNAs in the ontogeny of leukemias and lymphomas[J].Leuk lymphoma,2009,50(2):160-170.
  • 7Wang R,Wang Z,Yang J,et al.MicroRNA-451 functions as a tumor suppressor in human non-small cell lung cancer by targeting ras-related protein 14(RAB14)[J].Oncogene,2011,30(23):2644-2658.
  • 8Zheng T,Wang J,Chen X,et al.Role of microRNA in anticancer drug resistance[J].Int J Cancer,2010,126(1):2-10.
  • 9Wang J,Lu M,Qiu C,et al.TransmiR:a transcription factor-microRNA regulation database[J].Nucleic Acids Res,2010,38(1):D119-D122.
  • 10Wasserman WW,Sandelin A.Applied bioinformatics for the identification of regulatory elements[J].Nat Rev Genetics,2004,5(4):276-287.

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