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反转录病毒结合位点-1基因在急性淋巴细胞性白血病中的研究进展 被引量:1

Advances of ecotropic viral integration site 1 gene in acute lymphoblastic leukemia
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摘要 作为原癌基因,反转录病毒结合位点-1(EVI1)基因在急性髓系白血病(AML)中可因染色体易位或其他遗传学异常而高表达,最终导致预后较差.近年来,EVI1基因在急性淋巴细胞性白血病(ALL)中的研究逐渐增多,尤其在儿童ALL中的研究较多.EVI1基因高表达亦提示预后不良,且与年龄密切相关,但是其与混合谱系白血病(MLL)基因重排及BCR-ABL基因重排的关系有待进一步研究.研究ALL中EVI1基因的表达特点以及探索相应的靶向治疗药物是今后的重要研究方向. As an proto-oncogene,ecotropic viral integration site 1 (EVI1) gene is over-expressed in acute myeloid leukemia (AML) because of chromosomal translocation or other genetic abnormalities,finally cause poor prognosis.In recent years,an increasing research of the expression of EVI1 in acute lymphoblastic leukemia (ALL),especially in pediatric ALL.The overexpression of EVI1 gene also suggest a poor prognosis,which is closely relate to the age.But the relationship between the expression of EVI1 gene and mixed lineage leukemia (MLL) and BCR-ABL gene rearrangement needs to be further studied.Researching the expression of EVI1 gene in ALL and exploring targeted therapeutic agents are important research directions in the future.
作者 陆娇 刘丹丹
出处 《国际肿瘤学杂志》 CAS 2017年第8期626-628,共3页 Journal of International Oncology
基金 国家自然科学基金(81300424) 江苏省自然科学基金(BK20151231)
关键词 原癌基因 白血病 淋巴样 基因表达 反转录病毒结合位点-1基因 Proto-oncogene Leukemia,lymphoid Gene expression Ecotropic viral integration site 1 gene
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  • 1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:473
  • 2Groschel S, Schlenk RF, Engelmann J, et al. Deregulated expression of EVIl defines a poor prognostic subset of MLL-rearranged acute myeloid leukemias: a study of the German-Austrian Acute Myeloid Leukemia Study Group and the Dutch-Belgian-Swiss HOVON/ SAKK Cooperative Group [ J ]. J Clin Oncol, 2013,31 ( 1 ) :95-103.
  • 3Vfzquez I, Maicas M, Cervera J,et al. Down-regulation of EVIl is associated with epigenetic alterations and good prognosis in patients with acute myeloid leukemia [ J ]. Haematologica, 2011,96 ( 10 ) : 1448-1456.
  • 4Konantz M,Andre MC, Ebinger M, et al. EVI-1 modulates leukemo- genic potential and apoptosis sensitivity in human acute lymphoblastic leukemia[ J]. Leukemia,2013,27( 1 ) :56-65 .
  • 5Pallisgaard N, Holdand P, Riishcbj DC,et al. Multiplex reverse tran- scription-polymerase chain reaction for simultaneous screening of 29 Iranslocations and chromosomal aberrations in acute leukemia. Blood, 1998 ,92(2) :574-588.
  • 6De Weer A, Poppe B, Cauwelier B, et al. Screening for EVIl: ectopic expression absent in T-cell acute lymphoblastic leukemia patients and cell lines[ J ]. Cancer Genet Cytogenet , 2006, 171 : 79-80.
  • 7Ba Q, Zhou N, Duan J, et al. Dihydroartemisinin exerts its anticancer activity through depleting cellular iron via transferrin receptor-I [ J]. PLoS One,2012,7(8) : 042703.
  • 8Moura IC, Lepelletier Y, Amulf B ,et al. A neutralizing monoclonal antibody (mAb A24) directed agaimt the transferrin receptor induces apoptosis of tumor T lymphocytes from ATL patients[ J ]. Blood, 2004, 103(5) :1838-1845.
  • 9Koehler M, Bchm F, Hancock M, ct al. Expression of activation anti- gem cd38 and cdT1 is not clinically important in childhood acute lym- phoblastic leukemia[J]. Leukemia, 1993,7(1 ) :41-45.
  • 10Das Gupta A, Patil J, Shah VI. Transferrin receptor expression by blast cells in acute lymphoblastic leukemia correlates with white cell count and immunophenotype[J]. Indian J Med Res, 1996,104:226-233.

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