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BMI-1基因在儿童急性白血病中表达的意义 被引量:3

Expression of BMI-1 Gene in Children with Acute Leukemia and Its Clinical Significance
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摘要 目的研究BMI-l基因在儿童急性白血病患者中的表达及临床意义。方法收集2008年7月1日-2009年4月30日郑州大学第三附属医院和郑州市其他医院的初诊急性白血病患儿标本46例,对照组标本30例。实验经患儿监护人知情同意,并经医院伦理委员会批准。运用反转录-聚合酶链反应(RT-PCR)检测其外周血BMI-1 mRNA表达水平,应用SPSS12.0软件进行数据分析。结果1.BMI-l基因在儿童急性白血病中的表达水平显著高于对照组(P<0.05);2.粒细胞性白血病中该基因部分表达或弱表达,而各型B淋巴细胞性白血病中均有表达,且高于粒细胞性白血病(P<0.05);3.联合化疗未缓解组其表达水平高于缓解组,但二者比较差异无统计学意义(P>0.05),缓解后均未检测到BMI-1 mRNA;4.初治组、复发组与完全缓解组比较,前二者BMI-1 mRNA表达均显著高于后者(P<0.05);初治组、复发组与对照组比较差异有统计学意义(P<0.05),完全缓解组与对照组比较差异无统计学意义(P>0.05)。结论BMI-1基因在儿童急性白血病中表达增高,完全缓解者该基因表达水平趋于正常,提示BMI-1基因可能参与急性白血病的发生、发展过程,并可作为急性白血病的发病、复发及治疗和预后判断的指标之一。 Objective To study the expression of BMI-l gene in children with acute leukemia and its clinical significance.Methods The clinical specimens of 46 children with acute leukemia who were diagnosed lately in the Third Affiliated Hospital of Zhengzhou University and other hospitals in Zhengzhou from Jul.1,2008 to Apr.30,2009 were collected,while peripheral blood specimens of 30 healthy children were collected as control group.With the guardians′ informed consent,the experiment was approved through the hospital ethics committee.The level of BMI-1 mRNA′s expression was tested using reverse transcription-polymerase chain reaction(RT-PCR),while data were analyzed through the application of SPSS 12.0 statistical software.Results 1.The level of BMI-l gene′s expression in children with acute leukemia was significantly higher than that in control group(P〈0.05);2.Partial expression or weak expression of the gene in children with myelogenous leukemia was found,while universal expression was found in various types of B-lymphocytic leukemia,which was higher than that in myelocytic leukemia group(P〈0.05);3.The level of BMI-1 gene′s expression was higher in chemotherapy non-remission group than that in remission group,but the difference was not statistically significant(P〉0.05),after complete remission,BMI-1 mRNA was not detected in the 2 groups;4.Compared with the complete remission group,expression of BMI-1 mRNA in the untreated group and the recurrence group was significantly higher(P〈0.05);and expression of BMI-1 mRNA in the former two was significantly different with that in control group(P〈0.05);while there was no significant difference between the complete remission group and the control group(P〉0.05).Conclusions BMI-1 gene was highly expressed in children with acute leukemia,and the level of the gene expression in patients of complete remission normalized,which suggests that the gene may be involved in the occurrence and the development process of leukemia;therefore,it is possible to regard the gene as a molecular marker to evaluate the development,relapse and prognosis of the patients with acute leukemia.
出处 《实用儿科临床杂志》 CAS CSCD 北大核心 2010年第3期198-200,共3页 Journal of Applied Clinical Pediatrics
关键词 BMI-1基因 急性白血病 反转录-聚合酶链反应 儿童 B - cell - specific moloney murine leukemia virus insertion site 1 gene acute leukemia reverse transcription polymerase chain reaction child
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  • 1石太新,唐成和,李树军,赵光明,秦志强,赵卫星,贾汝贤.小儿急性白血病骨髓细胞Bcl-2和P^(53)蛋白的表达[J].新乡医学院学报,2001,18(1):12-14. 被引量:5
  • 2唐锁勤.美国儿童急性淋巴细胞性白血病治疗方案介绍[J].实用儿科临床杂志,2008,23(15):1219-1221. 被引量:2
  • 3李开春,吴晴.肿瘤干细胞相关研究进展[J].中华肿瘤防治杂志,2007,14(4):311-314. 被引量:4
  • 4顾龙君.儿童急性淋巴细胞白血病诊疗建议(第三次修订草案)[J].中华儿科杂志,2006,44(5):392-395. 被引量:485
  • 5Saeki M,Kobayashi D, Tsuji N, et al. Diagnostic importance of overexpression of Bmi - 1 mRNA in early breast cancers [J]. Int J Oncol, 2009,35(3) :511 -515.
  • 6Hosen N, Yamane T, Muijtjens M, et al. Bmi - 1 - green fluorescent protein - knock - in mice reveal the dynamic regulation of bmi - 1 expression in normal and leukemic hematopoietic cells[J]. Stem Cells ,2007, 25(7) :1635 - 1644.
  • 7Bhattacharyya J, Mihara K,Yasunaga S,et al. BMI - 1 expression is enhanced through transcriptional and posttranscriptional regulation during the progression of chronic myeloid leukemia[ J]. Ann Hematol,2009,88 (4) :333 -340.
  • 8Yang J,Chai L,Liu F,et al. Bmi - 1 is a target gene for SALIA in hematopoietic and leukemic cells [J]. Proc Natl Acad Sci U S A,2007,104 (25) : 10494 - 10499.
  • 9Lessard J, Sauvageau G. Polycomb group genes as epigenetic regulators of normal and leukemia hemopoiesis [ J ]. Exp Hematol, 2003,31 ( 7 ) : 567 - 585.
  • 10Chowdhury M, Mihara K, Yasunaga S ,et al. Expression of Polycombgroup (PcG) protein BMI - 1 predicts prognosis in patients with acute myeloid leukemia [ J ]. Leukemia,2007,21 (5) : 1116 - 1122.

二级参考文献33

  • 1邓永文,方加胜,李茗初,陈风华,刘劲芳,伍军,周向阳,方芳,卢明,陈成,周仁辉,曾飞跃.胶质瘤中肿瘤干细胞的分离、培养及鉴定[J].中国现代医学杂志,2005,15(16):2449-2452. 被引量:16
  • 2Reya T,Morrison S J,Clarke M F,et al.Stem cells,cancer,and cancer stem cells[J].Nature,2001,414(6859):105-111.
  • 3Bonnet D,Dick J E.Human acute myeloid leukemia is organized as a hierarchy that originates from a primitive hematopoietic cell[J].Nat Med,1997,3(7):730-737.
  • 4Al-Hajj M,Wicha M S,Benito-Hernandez A,et al.Prospective identification of tumorigenic breast cancer cells[J].Proc Natl Acad Sci USA,2003,100(7):3983-3988.
  • 5Singh S K,Clarke I D,Terasaki M,et al.Identification of a cancer stem cell in human brain tumors[J].Cancer Res,2003,63(18):5821-5828.
  • 6Bruce W R,Van Der Gaag H.A quantitative assay for the number of murine lymphoma cells capable of proliferation in vivo[J].Nature,1963,199:79-80.
  • 7Wodinsky I,Swiniarski J,Kensler C J.Spleen colony studies of leukemia L1210.IV.Sensitivities of L1210 and L1210/6-MP to triazenoimidazolecarboxamides-a preliminary report[J].Cancer Chemother Rep,1968,52(3):393-398.
  • 8Hamburger A W,Salmon S E.Primary bioassay of human tumor stem cells[J].Science,1977,197(4302):461-463.
  • 9Clarke R B,Anderson E,Howell A,et al.Regulation of human breast epithelial stem cells[J].Cell Prolif,2003,36(Suppl 1):45-58.
  • 10Ignatova T N,Kukekov V G,Laywell E D,et al.Human cortical glial tumors contain neural stem-like cells expressing astroglial and neuronal markers in vitro[J].Glia,2002,39(3):193-206.

共引文献491

同被引文献42

  • 1Martin LP,Hamilton TC,Schilder RJ.Platinum resistance:The role of DNA repair pathways[J].Clin Cancer Res,2008,14(5):1291-1295.
  • 2Fasano CA,Phoenix TN,Kokovay E,et al.Bmi-1 cooperates with Foxg1 to maintain neural stem cell self-renewal in the forebrain[J].Genes Dev,2009,23(5):561-574.
  • 3Louis DN,Ohgaki H,Wiestler OD,et al.The 2007 WHO classification of tumours of the central nervous system[J].Acta Neuropathol,2007,114(2):97-109.
  • 4Pouratian N,Schiff D.Management of low-grade glioma[J].Curr Neurol Neurosci Rep,2010,10(3):224-231.
  • 5Bhagwat NR,Roginskaya VY,Acquafondata MB,et al.Immunodetection of DNA repair endonuclease ERCC1-XPF in human tissue[J].Cancer Res,2009,69(17):6831-6838.
  • 6Song LB,Li J,Liao WT,et al.The polycomb group protein Bmi-1 represses the tumor suppressor PTEN and induces epithelial-mesenchymal transition in human nasopharyngeal epithelial cells[J].J Clin Invest,2009,119(12):3626-3636.
  • 7Bartels U,Baruchel S,Carret AS,et al.The use and effectiveness of temozolomide in children with central nervous system tumours:A survey from the Canadian Paediatric Brain Tumour Consortium[J].Curr Oncol,2011,18(1):e19-e24.
  • 8Chamberlain MC,Johnston SK,Glantz MJ.Neoplastic meningitis-rela-ted prognostic significance of the Karnofsky performance status[J].Arch Neurol,2009,66(1):74-78.
  • 9Blauwblomme T,Varlet P,Goodden JR,et al.Forniceal glioma in children(clinical article)[J].J Neurosurg Pediatr,2009,4(3):249-253.
  • 10Liu ZG,Chen HY,Cheng JJ,et al.Relationship between methylation status of ERCC1 promoter and radiosensitivity in glioma cell lines[J].Cell Biol Int,2009,33(10):1111-1117.

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