期刊文献+

急性白血病患儿混合谱系白血病基因重排阳性的生物学和临床特征 被引量:6

Clinical and molecular biologic characteristics of childhood acute leukemia with mixed lineage leukemia gene rearrangement
原文传递
导出
摘要 目的探讨儿童AL中混合谱系白血病(mixed lineage leukemia,MLL)基因重排的发生率、融合基因的常见类型及临床特征。方法利用巢式反转录聚合酶链反应检测MLL融合基因,对87例阳性患儿的骨髓细胞形态学、免疫学、分子生物学、染色体特征以及临床表现进行回顾性分析。结果儿童AL1209例中87例有MLL基因重排,其中ALL发生率为6.41%,AML发生率为9.36%。58例ALL均为B—ALL,28例AML中M517例,M45例,M24例,M3、M6各1例,混合性白血病1例,为髓系伴T淋巴系表达。76例进行染色体核型分析,45例(59.21%)可检出克隆性染色体异常,其中28例累计11q23(36.84%)。检测到7种融合基因亚型:MLL—AF9及dupMLL各25例,MLL—AF417例,MLL—AF109例,MLL—ENL8例,MLL—AF1q2例.MLL—AF61例。MLL-AF4、MLL—AF9、MLL—AF10、MLL—ENL及dupMLL在白血病类型、年龄及WBC计数比较差异均有统计学意义(P均〈0.05)。结论儿童MLL基因重排白血病ALL中以B.ALL多见,AML以M5、M4多见;最常见的融合基因亚型为MLL—AF9、MLL—AF4和dupMLL。MLL融合基因类型不同,可能表现为不同的临床特征,其中MLL—AF4、MLL—ENL可能多见于ALL,初诊WBC较高,发病年龄较小。 Objective To analyze the frequency of mixed lineage leukemia (MLL) gene rearrangement, the frequent types of fusion genes and clinical characteristics of childhood acute leukemia (AL) with MLL gene rearrangement. Methods Morphological and molecular characteristics of 87 AL patients with MLL gene rearrangement were studied and analyzed. MLL fusion gene was detected by way of reverse transcription polymerase chain reaction (RT- PCR). Results Eighty-seven cases with MLL gene rearrangement were found in 1209 AL patients with incidence of 6.41% and 9.36% respectively in ALL and in acute myelocytic leukemia (AML) respectively. Fifty-eight cases of ALL were all B-ALL,28 cases of AML included 17 cases of M5,5 cases of M4,4 cases of M2,1 case of M3 and 1 case of M6. While there was 1 case of mixed of lineage leukemia and myeloid and T-lymphoblastie antigen presentation. The clonal chromosomal aberration was detected in 45 out of 76 cases (59.21%) , and chromosome 11 q23 aberration were observed in 28 cases (36.84%). There were 7 different kinds of fusion genes, including MLL-AF9 in 25 cases, dupMLL in 25 cases, MLL-AF4 in 17 cases, MLL-AFIO in 9 cases, MLL-ENL in 8 cases, MLL-AFI q in 2 cases, and MLL-AF6 in 1 case. Among the cases of MLL-AF4, MLL-AF9, MLL-AF10, MLL-ENL and dupMLL, there were statistical differences in lineage, age and initial white blood cell count (WBC) ( all P 〈 0.05 ). Conclusions In childhood AL with MLL gene rearrangement, B-ALL is more common in ALL, whereas M5 and M4 are more common in AML. The common types of fusion genes are dupMLL, MLL-AF9 and MLL-AF4. Patients with the different kinds of MLL fusion gene may present different clinical characteristics. The most common ALL cases are those with MLL/AF4 and MLL/ENL who may be younger with higher WBC than the others.
出处 《中华实用儿科临床杂志》 CAS CSCD 北大核心 2013年第3期207-209,共3页 Chinese Journal of Applied Clinical Pediatrics
关键词 白血病 急性 混合谱系白血病 基因重排 融合基因 巢式反转录聚合酶链反应 儿童 Leukemia, acute Mixed lingeage leukemia Fusion gene Nested reverse transcription polymerase chain reaction Child
  • 相关文献

参考文献14

  • 1高超,李志刚.混合谱系白血病基因重排与急性白血病[J].中国小儿血液与肿瘤杂志,2010,15(3):104-107. 被引量:4
  • 2Liu HC,Shih LY,May Chen M J. Expression of HOXB genes is significantly different in acute myeloid leukemia with a partial tandem duplication of MLL vs.a MLL translocation:a cross-laboratory study[J].Cancer Genet,2011,(05):252-259.
  • 3赵杰,殷宇明,赵艳丽,孙媛,王静波,钟静,张弦,费新红,单褔香,刘红星,王彤,王卉,童春容,吴彤,陆道培.36例11q23/Mll融合基因白血病的分子生物学和临床特点分析[J].中国实验血液学杂志,2010,18(6):1381-1385. 被引量:3
  • 4沈志祥.血液疾病诊断学[M]上海:上海科学技术出版社,2006119-129.
  • 5Pallisgaard N,Hokland P,Riishoj DC. Multiplex reverse transcription-polymerase chain reaction for simultaneous screening of 29 translocations and chromosomal aberrations in acute leukemia[J].Blood,1998,(02):574-588.
  • 6Smith E,Lin C,Shilatifard A. The super elongation complex (SEC) and MLL in development and disease[J].Genes and Development,2011,(07):661-672.
  • 7赵峻峰,王立新,张秀珑.急性单核细胞白血病MLL基因与FAB分型及疗效的相关性研究[J].山东医药,2011,51(4):85-86. 被引量:6
  • 8De Braekeleer M,Morel F,Le Bris M J. The MLL gene and translocations involving chromosomal band 11q23 in acute leukemia[J].Anticancer Research,2005,(3B):1931-1944.
  • 9Xu L,Zhao WL,Xiong SM. Molecular cytogenetic characterization and clinical relevance of additional,complex and/or variant chromosome abnormalities in acute promeyelocytic leukemia[J].Leukemia:Official Journal of the Leukemia Society of America,Leukemia Research Fund,U.K,2001.1359-1368.
  • 10Balgobind BV,Zwaan CM,Pieters R. The heterogeneity of pediatric MLL-rearranged acute myeloid leukemia[J].Leukemia:Official Journal of the Leukemia Society of America,Leukemia Research Fund,U.K,2011,(08):1239-1248.

二级参考文献75

  • 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:472
  • 2Chowdhury T,Brady HJ.Insights from clinical studies into the role of the MLL gene in infant and childhood leukemia.Blood Cells Mol Dis,2008,40:192-199.
  • 3Saarinen-Pihkala UM,Gustafsson G,Carlsen N,et al.Outcome of children with high-risk acute lumphoblastic leukemia (HR-ALL):Nordic results on an intensive regimen with restricted central nervous system irradiation.Pediatr Blood Cancer,2004,42:8-23.
  • 4Marschalek R,Nilson I,Lchner K,et al.The structure of the human ALL-1/MLL/HRX gene.Leuk Lymphoma,1997,27:417-428.
  • 5Nilson I,Lchner K,Siegler G,et al.Exon/intron structure of the human ALL-1(MLL) gene involved in translocations to chromosomal region 11q23 and acute leukaemias.Br J Haematol,1996,93:966-972.
  • 6Ayton PM,Cleary ML.Molecular mechanisms of leukemogenesis mediated by MLL fusion proteins.Oncogene,2001,20:5695-5707.
  • 7Daser A,Rabbitts TH.Extending the repertoire of the mixed-lineage leukemia gene MLL in leukemogenesis.Genes Dev,2004,18:965-974.
  • 8Mitterbauer-Hohendanner G,Mannhalter C.The biological and clinical significance of MLL abnormalities in haematological malignancies.Eur J Clin Invest,2004,34 Suppl 2:12-24.
  • 9Hsieh JJ,Cheng EH,Korsmeyer SJ.Taspase1:a threonine aspartase required for cleavage of MLL and proper HOX gene expression.Cell,2003,115:293-303.
  • 10Hsieh JJ,Ernst P,Erdjument-Bromage H,et al.Proteolytic cleavage of MLL generates a complex of N-and C-terminal fragments that confers protein stability and subnuclear localization.Mol Cell Biol,2003,23:186-194.

共引文献21

同被引文献50

引证文献6

二级引证文献11

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部