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Ph阴性骨髓增殖性肿瘤病人JAK2基因表达及意义

THE EXPRESSION AND ITS CLINICAL SIGNIFICANCE OF JAK2 IN Ph-NEGATIVE MYELOPROLIFERATIVE NEOPLASMS
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摘要 目的探讨Ph阴性的骨髓增殖性肿瘤(MPN)病人骨髓细胞中Janus激酶2(JAK2)基因的表达及其临床意义。方法用常规染色体分析法检测MPN病人的染色体,选择Ph阴性病人16例作为观察组,继发性红细胞增多症和继发性血小板增多症病人12例为病例对照组,以健康人5例为正常对照组,应用半定量RT-PCR方法分别检测各组JAK2mRNA的水平。结果 Ph阴性MPN病人JAK2mRNA的平均表达水平为0.63±0.35,病例对照组为0.62±0.43,正常对照组为0.60±0.25,各组间相比较差异无统计学意义(P>0.05)。结论JAK2mRNA的检测不能单独作为MPN与继发性红细胞增多症及继发性血小板增多症的鉴别诊断指标。 Objective To investigate the expression of JAK2 and its clinical significance in patients with Ph-negative myeloproliferative neoplasms(MPN). Methods A conventional karyotype analysis was used to detect the chromosomes in patients with MPN,those 16 with Ph-negative were enrolled as observation group,and five healthy subjects served as normal control.JAK2 mRNA levels were detected in each group by employing semi-quantitative reverse transcriptase polymerase chain reaction(RT-PCR) technique. Results The average levels of JAK2 mRNA in Ph-negative patients,case controls and healthy controls were 0.63±0.35,0.62±0.43 and 0.60±0.25,respectively.The differences of JAK2 mRNA levels between MPN patients and case controls and healthy controls were not significant(P〈0.05). Conclusion The JAK2 mRNA level can not be used alone as a diagnosis index in the differential diagnosis among MPN,secondary erythrocytosis,and secondary thrombocythemia.
出处 《齐鲁医学杂志》 2012年第2期120-122,124,共4页 Medical Journal of Qilu
关键词 JANUS激酶2 费城染色体 骨髓增殖性疾病 诊断 鉴别 Janus kinase 2 Philadelphia chromosome myeloproliferative disorders diagnosis differential
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  • 1DEININGER M W,GOLDMAN J M,MELO J V.The mo-lecular biology of chronic myeloid leukemia[J].Blood,2000,96(10):3343-3356.
  • 2LEVINE R L,WADLEIGH M,COOLS J,et al.Activatingmutation in the tyrosinekinase JAK2in polysythemia vera,es-sential thrombocythemia,and myeloid metaplasia with myelo-fibrosis[J].Cancer Cell,2005,7:387-397.
  • 3KRALOVICS R,PASSAMONTI F,BUSER A S,et al.Again of function mutation in JAK2is frequently foundingatients with myeloprofiferative disorders[J].N Engl J Med,2005,352:1779-1790.
  • 4BAXTER E J,SCOTT L M,CAMPBEL P J,et al.Acquiredmutation of the tyrosine kinase JAK2in human myeloprolifer-ative disorders[J].Lancet,2005,365:1054-1061.
  • 5杨颉,刘竹珍,吴春梅,赵洪国,陈兵,管洪在.慢性粒细胞白血病染色体核型分析及其临床意义[J].青岛大学医学院学报,2009,45(1):52-53. 被引量:6
  • 6宫本法,王建祥.JAK2 V617F突变与真性红细胞增多症发生[J].国际输血及血液学杂志,2006,29(5):403-406. 被引量:5
  • 7潘湘涛,吴锦昌.JAK2基因突变与骨髓增殖性疾病[J].中国医学文摘(内科学),2006,27(4):305-308. 被引量:6
  • 8KAUSHANSKY K.On the molecular origins of the chronicmyeloproliferative disorders:it all makes sense[J].Blood,2005,105(11):4187-4190.
  • 9PARGANAS E,WANG D,STRAVOPODIS D,et al.Jak2isessential for signaling through a variety of cytokine receptors[J].Cell,1998,93(3):385-395.
  • 10NEUBAUER H,CUMANO A,MLLER M,et al.Jak2de-ficiency defines an essential developmental checkpoint in defini-tive hematopoiesis[J].Cell,1998,93(3):397-409.

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