期刊文献+

INK4系列抑癌基因纯合子缺失、甲基化与白血病预后的实验研究 被引量:2

Study on pl6, p15, p18 and p19 homozygous deletion and methylation in leukemia
原文传递
导出
摘要 目的研究INK4系列抑癌基因纯合子缺失、甲基化与白血病预后的关系。方法采用聚合酶链反应(PCR)研究p16基因家族在白血病中纯合子缺失,应用甲基化敏感限制内切酶HpaII结合PCR技术研究自血病患者p16、p15、p18、p19基因甲基化状况,用单因素、多因素Logistic回归分析其基因失活与急性白血病(AL)预后的关系。结果基因表达组治疗有效27例(84.38%),基因失活组治疗有效11例(28.95%),基因表达组治疗有效率明显高于基因失活组(P〈0.001)。单因素、多因素Logistic回归分析结果显示p16、p15基因失活化疗有效率明显低于基因表达组。结论p16、p15基因失活可作为AL病程进展、复发、预后的指标之一。 Objective To explore the correlation between the family of pl6 gene inactivation and prognosis of leukemia, and then to clarify, the pathogenesis of leukemia, and monitor process of leukemia. Methods We used polymerase chain reaction(PCR) to study p16, p15, p18, p19 gene homozygous deletion, by using methylation-sensitive enzyme and PCR technology to iuvestigate p16, p15, p18, p19 gene methylation in leukemia. Results The effective rate with p16 and p15 gene aetiviation was 27 cases (84.38 %), the effective rate with p16 and p15 gene inaetiviation was 11 cases (28.95 %), and the total effective rate with p16 and p15 gene aetiviation was higher than p16 and p15 gene inactivation.In case to use single and muhi factor Logistic regression, effective rate in cases with p16 and p15 gene inactiviation was lower than that with p16 and p15 gene activation. Conclusion It might be one of parameters for forcasting progression, relapse and prognosis in AL.
出处 《白血病.淋巴瘤》 CAS 2010年第4期230-233,共4页 Journal of Leukemia & Lymphoma
关键词 白血病 基因 基因沉默 甲基化 治疗结果 Leukemia Genes Gene silencing Methylation Treatment outcome
  • 相关文献

参考文献5

  • 1(美)萨姆布鲁克 J,弗里奇 EF,曼氏阿蒂斯 T,著.黄培堂主译.分子克隆实验指南.3版.北京:科学出版社,1996:577-596.
  • 2张之南.血液病诊断及疗效标准.2版.北京:科学出版社,1999:168-179.
  • 3Kamb A,Gruis NA,Weaver-Feldhaus J,et al.A cell cycle regulator potentially involved in genesis of many tumor types.Science,1994,264:436-440.
  • 4Yamada Y,Hatta Y,Murata K,et al.Deletions of p15 and/or p16 genes as a poor prognosis factor in adult T-cell leukemia.J Clin Oncol,1997,15:1778-1785.
  • 5Heyman M,Rasool O,Borgonovo B,et al.Prognostic importance of p15INK4B and p16INK4A gene inactivation in childhood acute lymphocytic leukemia.J Clin Oncol,1997,14:1512-1520.

共引文献7

同被引文献25

  • 1杨少辉,戴冬秋.甲基化特异性PCR技术的分析及改良[J].肿瘤研究与临床,2006,18(9):594-595. 被引量:7
  • 2张之南.血液病诊断及疗效标准.2版.北京:科学出版社,1999:168-179.
  • 3Kamb A, Gruis NA, Weaver-Feldhaus J, et al. A cell cycle regulator potentially involved in genesis of many tumor types. Science, 1994, 264:436-440.
  • 4Herman JG, Graft JR, Myohanen S, et al. Methylation-specific PCR:a novel PCR assay for methylation status of CpG island. Proc Natl Acad Sci U S A, 1996,93:9821-9826.
  • 5Li LC, Dahiya R. MethPrimer:. designing primers for methylation PCRs.Bioinformaties, 2002 , 18:1427-1431.
  • 6Chim CS, Wong AS, Kwong YL. Epigenetic inactivation of INK4/CDK/RB cell cycle pathway in acute leukemias. Ann Hematol, 2003 , 82:738-742.
  • 7Thomas X, Teillon MH, Belhabri A, et al. Hypermethylation of calcitonin gene in adult acute leukemia at diagnosis and during complete remission. Hematol Cell Ther, 1999, 41:19-26.
  • 8Takeuchi S, Bartram CR. Analysis of a family of cyclin-dependent kinase inhibitors:p15/MTS2/INK4B ,pl6/MTS1/INK4A, and p18 genes in acute lymphoblastic leukemia of childhood. Blood, 1995, 86:755-760.
  • 9林东军,郑永江,方志刚,范蕊芳,刘加军,林玉辉.急性白血病p53基因P1启动子区域DNA甲基化研究[J].中国病理生理杂志,2008,24(7):1327-1330. 被引量:10
  • 10陈恩,肖建华.p15基因的研究进展[J].肿瘤学杂志,2009,15(3):246-247. 被引量:5

引证文献2

二级引证文献3

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