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垂体瘤转化基因在急性淋巴细胞白血病患者中表达的研究

Expression of Pituitary Tumor Transforming Gene in Patients with Acute Lymphoblastic Leukemia
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摘要 本研究旨在探索垂体瘤转化基因(pituitary tumor-transforming gene,PTTG)在急性淋巴细胞白血病(acutelymphoblastic leukemia,ALL)患者中的表达及其与ALL发病机理的关系,同时探讨PTTG在Ph1染色体阳性和阴性ALL中的表达是否存在差异性。采用实时荧光定量PCR方法检测28例ALL患者及28例正常对照骨髓中PT-TG的表达水平。结果表明:ALL患者PTTG的表达水平(1.9428E5±1.8372E5)明显高于正常对照组(4.5766E3±1.1817E3)(P<0.05),一个周期诱导缓解治疗后达完全缓解(complete remission,CR)患者中PTTG的初始表达水平低于未缓解(non-complete remission,non-CR)患者;Ph1染色体阳性ALL(Ph1+ALL)患者中PTTG的初始表达水平高于Ph1染色体阴性ALL(Ph1-ALL)患者。结论:PTTG的过度表达可能和ALL的发生发展有关,可能与Ph1染色体阳性ALL的发生关系更加密切,这为ALL的发病机制及其基因靶向治疗的研究提供了新的思路。 The aim of this study was to explore the expression of pituitary tumor-transforming gene(PTTG) in acute lymphoblastic leukemia(ALL)and its relationship with the pathogenesis of ALL,as well as study the difference of the PTTG expression in ALL patients with Ph1 chromosome and without Ph1 chromosome.The mRNA expressions of PTTG in bone marrow from 28 patients with ALL and 28 normal controls were quantitatively detected by real-time quantitative polymerase chain reaction(real-time PCR).The results indicated that the expression of PTTG mRNA was significantly higher in ALL patients(1.9428E5±1.8372E5) than that in normal controls(4.5766E3±1.1817E3)(P〈0.05).The expression of PTTG mRNA was higher in Ph1 chromosome positive patients.The initial expression of PTTG mRNA was lower in patients achieved complete remission than that in patients with non-complete remission.It is concluded that the overexpression of PTTG may be related to the progression and genesis of ALL.Overexpression of PTTG may be intimately related to the progression and genesis of Ph1 chromosome positive ALL.It provides a new ideas to research the pathogenesis and genic target treatment of ALL.
出处 《中国实验血液学杂志》 CAS CSCD 北大核心 2013年第4期835-838,共4页 Journal of Experimental Hematology
基金 福建省厦门市卫生局青年科研创新资助项目(编号A0000241) 厦门大学985博士点基金资助
关键词 垂体瘤转化基因 急性淋巴细胞白血病 ph1染色体 pituitary tumor-transforming gene acute lymphoblastic leukemia phl chromosome
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参考文献8

  • 1Pei L, Melmed S. Isolation and characterization of a pituitary tumor-transforming gene( PTrG). Mol Endocrinol, 1997 ; 11 ( 4 ) : 433 -441.
  • 2Dominguez A, Ramos-Morales F, Romero F, et al. hpttg, a human homologue of rat pttg, is overex-pressed in Hemato-poietic neoplasms. Evidence for a transcriptional activation function of hPTTG. Oncogene, 1998 ; 17 ( 17 ) :2187 - 2193.
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二级参考文献9

  • 1陈萍,丛雅琴,王昭,林华伟,侯明.急性白血病患者垂体瘤转化基因和c-myc基因表达的研究[J].中华血液学杂志,2005,26(7):427-428. 被引量:7
  • 2Pei L, Melmed S. Isolation and characterization of a pituitary tumor-transforming gene ( PTTG ). Mol Endocrinlol, 1997 ; 11 (4) : 433 - 441.
  • 3Dominguez A, Ramos-Morales F, Romero F, et al. Hpttg, a human hornologue of rat pttg, is overexpressed in hematopoietic neoplasms. Evidence for a transcriptional activation function of hPTTG. Oncogene, 1998 ;17(17) :2187 -2193.
  • 4Zhang X, Horwitz GA, Prezant TR, et al. Structure, expression, and function of human pituitary tumor-transforming gene(PTTG). Mol Endocrinol, 1999 ; 13 ( 1 ) : 156 - 166.
  • 5Strausber RL, Dalai CA, Klansner RD. New opportunities for uncovering the molecular basis of cancer. Nat Genet, 1997;15Spec No: 415 -416.
  • 6Jallepalli PV, Waizenegger IC, Bunz F, et al. Securin is required for chromosomal stability in human cells. Cell, 2001 ; 105 (4) :445 - 457.
  • 7Bernal JA, Luna R, Espina A, et al. Human securin interacts with p53 and modulates p53-mediated transcriptional activity and apoptosis. Nat Genet,2002 ;32(2) :306 -311.
  • 8Pei L, Melmed S. Isolation and characterization of a pituitary tumortransforming gene(PTYG). Mol Endocrinol, 1997,11:433-441.
  • 9Pei L. Identification of c-myc as a down-stream target for pituitary tumor-transforming gene. J Biol Chem,2001,276: 8484-8491.

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