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急性和慢性白血病Livin基因表达的研究 被引量:3

Expression of Livin gene in acute leukemia and chronic myelocytic leukemia
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摘要 目的:研究Livin基因在急、慢性白血病中的表达,探讨其临床意义。方法:采用半定量逆转录-聚合酶链反应(RT-PCR)检测91例急性白血病(AL)和17例慢性粒细胞性白血病(CML)患者Livin mRNA的表达水平,21名健康人的标本作正常对照。结果:初治AL患者中Livin的表达较正常对照明显升高,治疗缓解后的表达水平下降,复发时又再次升高;慢性粒细胞白血病慢性期(CML-CP)、加速/急变期(CML-AP/BP)患者Livin的表达水平均高于正常对照组;初治AL患者中,Livin阳性的患者缓解率低于表达阴性的患者。结论:Livin基因的过度表达参与了急、慢性白血病的发病,并且是AL复发的高危因素;Livin基因的高表达是判断急性白血病预后不良的指标之一。 Objective: To investigate the expression of Livin in leukemia and the prognostic significance in acute leukemia (AL) in adults. Methods: The expression of Livin mRNA was measured in 91 AL and 17 chronic myelocytic leukemia (CML) patients by semi-quantity reverse transcription polymers chain reaction (RT-PCR). 21 healthy adults were also measured as normal control. Results: The expression of Livin in de novo AL was higher than that in normal control, while it decreased in patients with complete remission. In relapsed patients, the expression of Livin increased again. The level of Livin mRNA in CML was significantly higher than that in normal controls. In AL patients, the CR rate in Livin ^+ cases was lower than that in Livin cases. Conclusions: Overexpression of Livin may play a synergic role in the pathogenesis of leukemia and may be a high risk factor for relapse in AL. High expression of Livin can serve as one of the markers of poor prognosis in AL.
出处 《军医进修学院学报》 CAS 2009年第1期99-101,共3页 Academic Journal of Pla Postgraduate Medical School
基金 河北省卫生厅医学科学研究重点课题计划指导项目(07209) 河北省科学技术研究与发展计划项目(072761241)
关键词 白血病 凋亡抑制蛋白 逆转录聚合酶链反应 预后 leukemia IAP RT -PCR prognosis
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  • 1Dukett CS. IAP proteins: sticking it to Smac [ J ]. Biochem J, 2005, 385(pt1) :1-2.
  • 2Qiuping z, Jei X, Youxin J, et al. CC chemokine ligand 25 enhances resistance to apoptosis in CD4^ + T Cells from patients with T-Cell lineage acute and chronic lymphocytic leukemia by means of Livin activation[J]. Cancer Res, 2004, 64(20) :7579-7587.
  • 3Qiuping Z, Jei X, Youxin J, et al. Selectively frequent exprssion of CXCR5 enhances resists:nee to apoptosis in CD8 ( + ) CD34 ( + ) T cells from patients with T-cell-lineage acute lymphocytic leukemia[J]. Oncogene, 2005, 24(4):573-584.
  • 4Cmkovic-Mertens I, Hoppe-Seyler F, Butz K. Induction of apoptosis in tumor cells by siRNA-mediated silencing of the Livin/MLIAP/KIAP gene[J]. oncogene, 2003, 22(51) :8330-8336.

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