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血浆miR-128在胶质母细胞瘤诊断中的作用研究

Role of plasma miR-128 in diagnosis and treatment of glioblastoma
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摘要 目的探讨血浆中miR-128在胶质母细胞瘤诊断的作用。方法收集30例不同级别胶质瘤病人的肿瘤组织和血浆标本作为实验组,同时收集健康成年人的脑组织和血浆作为正常对照组。利用实时定量PCR,检测组织和血浆中miR-128的表达水平。结果 miR-128在各级胶质母细胞瘤组织中的表达较正常对照组均明显降低(均P<0.005),且与肿瘤的病理级别呈负相关(r=-0.497,P<0.001)。miR-128在胶质母细胞瘤病人血浆中的表达明显低于正常对照组(P<0.001)。血浆miR-128诊断胶质母细胞瘤的特异性和敏感性分别为90%和100%。结论 miR-128可作为胶质母细胞瘤的一种新型血浆标记物,用于指导诊断。 Objective To explore the role of plasma miR-128 in glioblastoma. Methods The samples of tumor tissue and plasma were collected from 30 patients with different grade glioblastoma as experimental group. The samples of brain tissue and plasma were collected from 10 healthy adults as normal control group. The expressions of miR-128 in tissue and plasma were tested by real-time quantitative polymerase chain reaction (RT-PCR). Results The expressions of miR-128 in tissue of glioblastoma patients in experimental group were lower than those in normal control group (all P 〈 0.005). The expression of miR-128 in tissue of glioblastoma was negatively related to the pathological grade of tumor (r = -0.479, P 〈 0.001). The expressions of miR-128 in plasma of glioblastoma patients in experimental group were lower than those in normal control group (P 〈 0.001). The specificity and sensitivity of plasma miR-128 in the diagnosis of glioblastoma were 90% and 100%. Conclusion The plasma miR-128 can be used as a novel biomarker of glioblastoma, which can guide the treatment.
出处 《中国微侵袭神经外科杂志》 CAS 2014年第6期280-282,共3页 Chinese Journal of Minimally Invasive Neurosurgery
基金 天津市科委重点项目(编号:14JCZDJC35600) 天津市科技支撑计划(编号:12ZCDZSY17700) 天津市卫生局重点科技基金(编号:2011KR11) 天津市卫生局科技攻关项目(编号:11KG115) 卫生部临床重点学科专项基金
关键词 神经胶质瘤 微RNAS 血浆 诊断 glioma MicroRNAs plasma diagnosis
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参考文献20

  • 1李仲颖,牛朝诗.Nanog基因与神经胶质瘤的研究进展[J].中国微侵袭神经外科杂志,2013,18(10):475-477. 被引量:4
  • 2Fortunato O, Boeri M, Verri C, et al. Assessment of circulating microRNAs in Plasma of lung cancer patients [J]. Molecules, 2014, 19(3): 3038-3054.
  • 3Fire A, Xu S, Montgomery MK, et al. Potent and specific genetic interference by double-stranded RNA in Caenorh- abditis elegans [J]. Nature, 1998, 391(6669): 806-811.
  • 4Bartel DP. MicroRNAs: genomics, biogenesis, mechanism and function [J]. Cell, 2004, 116(2): 281-297.
  • 5Ambros V. The function of animal microRNAs [J]. Nature, 2004, 431(7006): 350-355.
  • 6Plasterk RH. Micro RNAs in animal development [J]. Cell, 2006, 124(5): 877-881.
  • 7Lu J, Getz G, Miska EA, et al. MicroRNA expression profiles classify human cancers [J]. Nature, 2005, 435 (7043): 834-838.
  • 8Esquela-Kerscher A, Slack FJ. Oncomirs-microRNAs with a role in cancer [J]. Nat Rev Cancer, 2006, 6(4): 259-269.
  • 9施秀华,孙青芳.微小RNA与垂体腺瘤发病机制的相关研究进展[J].中国微侵袭神经外科杂志,2011,16(7):329-332. 被引量:4
  • 10Mitchell PS, Parkin RK, Kroh EM, et oi. Circulating microRNAs as stable blood-based markers for cancerdetection [J]. Proc Natl Acad Sci USA, 2008, 105(30): 10513-10518.

二级参考文献25

  • 1Guangjin Pan,James A Thomson.Nanog and transcriptional networks in embryonic stem cell pluripotency[J].Cell Research,2007,17(1):42-49. 被引量:52
  • 2Lee RC, Feinbaum RL, Ambros V. The C.elegans heterochronic gene lin-4 encodes small RNAs with antisense complementarity to lin-14 [J]. Cell, 1993, 75(5): 843-854.
  • 3McDowell BD, Wallace RB, Camahan RM, et al. Demographic differences in incidence for pituitary adenoma [J]. Pituitary, 2010, 14(1): 23-30.
  • 4Ezzat S, Asa SL. Mechanisms of disease: the pathogenesis of pituitary tumors [J]. Nat Clin Pract Endocrinol Metab, 2006, 2(4): 220-230.
  • 5Cheng AM, Byrom MW, Shelton J, et ol. Antisense inhibi- tion of human miRNAs and indications for an involvement of miRNA in cell growth and apoptosis [J]. Nucleic Acids Res, 2005, 33(4): 1290-1297.
  • 6Bottoni A, Piccin D, Tagliati F, et al. MiR-15a and miR-16-1 down-regulation in piaxitary adenomas [J]. J Cell Physiol, 2005, 204(1): 280-285.
  • 7Bottoni A, Zatelli MC, Ferracin M, et ol. Identification of differentially expressed microRNAs by microarray: a possible role for microRNA genes in pituitary adenomas [J]. J Cell Physiol, 2007, 210(2): 370-377.
  • 8Asa SL, Ezzat S. The cytogenesis and pathogenesis of pituitary adenomas [J]. Endocr Rev, 1998, 19(6): 798-827.
  • 9Amaral FC, Tortes N, Saggioro F, et al. MicroRNAs differentially expressed in ACTH-secreting pituitary tumors [J]. J Clin Endocrinol Metab, 2009, 94(1): 320-323.
  • 10Nikiforova MN, Tseng GC, Steward D, et al. MicroRNA expression profiling of thyroid tumors: biological significance and diagnostic utility [J]. J Clin Endocrinol Metab, 2008, 93(5): 1600-1608.

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