期刊文献+

BCR-ABL融合基因与慢性粒细胞白血病的相关性分析

Correlation analysis between BCR-ABL fusion gene and chronic myeloid leukemia
下载PDF
导出
摘要 目的 探究BCR-ABL融合基因在诊断慢性粒细胞白血病(CML)及临床分期的价值。方法 回顾性分析近年本院收治的59例CML患儿的临床资料,以对比分析CML与健康儿童的BCR-ABL融合基因突变率及不同分期BCR-ABL突变率。结果 观察组BCR-ABL突变率为89.8%,而对照组为阴性(P<0.01);CML慢性期、缓解期、加速期、急变期的BCR-ABL突变率分别为96.8%、25.0%、85.7%、100.0%。结论 BCR-ABL融合基因可作为CML诊断及分期的重要检测指标,对临床诊断、并根据临床分期指导治疗有积极价值。 Objective To explore the value of BCR-ABL fusion gene in the diagnosis of chronic myeloid leukemia(CML)and clinical staging.Methods The clinical data of 59 children with CML admitted to our hospital in recent years were analyzed retrospectively.The mutation rates of BCR-ABL fusion gene and BCRABL mutation rates in different stages were compared between CML and healthy children.Results The mutation rate of BCR-ABL in the observation group was 89.8%,while that in the control group was negative(P<0.01);the mutation rates of BCR-ABL in chronic phase,remission phase,acceleration phase,and acute phase were 96.8%,25.0%,85.7%,and 100.0%respectively.Conclusion BCR-ABL fusion gene can be used as an important marker for the diagnosis and staging of CML,and has positive value for clinical diagnosis and treatment according to clinical staging.
作者 王金 Wang Jin(Children’s Hospital Affiliated to Zhengzhou University,Henan Provincial Key Laboratory of Children’s Genetics and Metabolic Diseases,Zhengzhou Children’s Hospital,Zhengzhou 450018,China)
出处 《国际医药卫生导报》 2019年第2期225-227,共3页 International Medicine and Health Guidance News
关键词 BCR-ABL融合基因 慢性粒细胞白血病 诊断 分期 BCR-ABL fusion gene Chronic myeloid leukemia Diagnosis Staging
  • 相关文献

参考文献7

二级参考文献95

  • 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:477
  • 2秦先念,刘红,雷婷,陈幸华,孔佩艳,张曦,高蕾,张诚,王武.不典型慢性髓细胞白血病(aCML)1例[J].重庆医学,2007,36(10):1003-1003. 被引量:2
  • 3Nowell PC, Hungerford DA. Chromosome studies on normal and leukemic human leukocytes[J]. J Natl Cancer Inst, 1960,6 (25) : 85-109. 被引量:1
  • 4Gambacorti-Passerini CB, Gunby R H, Piazza R, et al. Molecular mechanisms of resistance to imatinib in Philadel- phia-chromosome-positive leukaemias [J]. Lancet Oncol, 2003,4(2) : 75-85. 被引量:1
  • 5Shah NP, Nicoll JM, Nagar B, et al. Multiple BCR-ABL kinase domain mutations confer polyclonal resistance to the tyrosine kinase inhibitor imatinib (STI571) in chronic phase and blast crisis chronic myeloid leukemia[J]. Cancer Cell,2002,2(2) :117-125. 被引量:1
  • 6Hughes T,Deininger M, Hochhaus A, et al. Monitori.ng CML patients responding to treatment with tyrosine ki- nase inhibitors:review and recommendations for harmonizing current methodology for detecting BCR-ABL tran- scripts and kinase domain mutations and for expressing results[J]. Blood,2006,108(1) :28-37. 被引量:1
  • 7Velev N,Cortes J ,Champlin R,et al. Stem cell transplan- tation for patients with chronic myeloid leukemia resistant to tyrosine kinase inhibitors with BCR-ABL kinase do- main mutation T315I[J]. Cancer, 2010, 116 (15): 3631- 3637. 被引量:1
  • 8Wongboonma W, Thongnoppakhun W, Auewarakul CU. A single-tube allele specific-polymerase chain reaction to detect T315I resistant mutation in chronic myeloid leukemia patients[J]. J Hematol Oncol, 2011,4 (7): 7. 被引量:1
  • 9Yin L,Dittman D,Chenn A. Rapid quantitative detection of the T315I mutation in patients with chronic myelogenous Ieukemia[J]. Diagn Mol Pathol, 2012,21 (1):34-39. 被引量:1
  • 10O'Hare T, Shakespeare WC, Zhu X, et al. AP24534, a pan-BCR-ABL inhibitor for chronic myeloid leukemia, potently inhibits the T315I mutant and overcomes mutation- based resistance[J]. Cancer Cell,2009,16(5):401 412. 被引量:1

共引文献35

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