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miR-221和miR-222在急性髓细胞白血病初发患者中的表达研究 被引量:3

The Expression and Significance of miR-221 and miR-222 in the Acute Myeloid Leukemia.
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摘要 目的探讨miR-221和miR-222在急性髓细胞白血病(AML)骨髓有核细胞中的表达及意义。方法选择16例AML初发患者和44例非白血病患者骨髓标本,分离有核细胞,抽提总RNA,以U6为内参,采用茎环Realtime RT-PCR法检测并比较AML和非白血病患者骨髓有核细胞中miR-221和miR-222的表达,同时比较这两种miRNAs在AML中M3、M4和M5三种亚型间的表达水平。结果 miR-221和miR-222在AML初诊患者骨髓中相对表达量(N=2-ΔCt)明显高于非白血病患者组(P<0.05);这两种miRNAs在M5型AML患者表达最高,但在AML三种亚型间表达水平未见显著的统计学意义(P>0.05)。结论 miR-221和miR-222有可能在为AML的诊断、治疗和预后上,提供一个新的标准和靶点指标。 Objective To investigate the expression and clinical significance of miR - 221 and miR - 222 in the marrow of acute myeloid leukemia(AML). Methods Marrow tissues from 16 newly diagnosed AML patients and 44 non - leukemia (NL) patients were collected and mononucleated cell were separated. Total RNA from nucleated cells of these samples were extracted and analyzed for miR - 221 and miR - 222 expression by stem - loop real - time RT - PCR. The differences in subtypes M3, M4 and M5 patients and the change of miR -221 and miR -222 expression in newly diagnosed AML patients were further analyzed. Results Expression levels of miR -221 and miR - 222 were significantly higher in marrow tissues of AML patients before chemotherapy than the levels in those of non - leukemia patients (P 〈0.05). Both miR-221 and miR-222 expression in the M5 of AML were the highest among them, but this difference in subtypes M3, M4 and M5 patients was not statistically significant(P 〉 0.05). Conclusion miR -221 and miR -222 may play an im- portant role in the development and progression of AML and the level of miR - 221 and miR - 222 expression may be a potential target for the diagnosis, treatment and prognosis of AML.
出处 《医学研究杂志》 2011年第6期110-113,共4页 Journal of Medical Research
关键词 MIR-221 miR-222急性髓细胞白血病 MieroRNA miR - 221 miR - 222 Acute myeloid leukemia
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参考文献13

  • 1Mehzer P S. Cancer genomics:small RNAs with big impact s. Nature, 2005,435 (7043) :745 -746.
  • 2Chen CZ, Li L, Lodish HF,et al. MicroRNAs modulate hematopoietic lineage differentiation. Science,2004, 303 (5654) :83 - 86.
  • 3Cheng A M, Byrom M W, Shelton J, et al. Antisense inhibition of human miRNAs and indications for an involvement of miRNA incell growth and apoptosis. Nucleic AcidsRes, 2005, 33 (4) :1290 -1297.
  • 4Garzon R, Volinia S, Liu C G, et al. MicroRNA signatures associated with cytogenetics and prognosis in acute myeloid leukemia. Blood, 2008,111 (6) :3183 -3189.
  • 5Garzon R, Garofalo M, Martelli M P, et al. Distinctive microRNA signature of acute myeloid leukemia bearing cytoplasmic mutatednu- cleophosmin. Proc Natl Acad Sci USA, 2008, 105 (10) :3945 -3950.
  • 6Jonqen - Lavrencic M, Sun S M, Dijkstra M K, et al. MicroRNA expression profiling in relation to the genetic heterogeneity of aeutemy- eloid leukemia. Blood, 2008, 111 (10) :5078 - 5085.
  • 7Garzon R, Volinia S, Liu C G, et al. MicroRNA signatures associated with cytogenetics and prognosis in acute myeloid leukemia. Blood, 2008, 111(6) :3183 -3189.
  • 8Garzon R, Garofalo M, Martelli M P, et al. Distinctive microRNA signature of acute nayeloid leukemia bearing cytoplasmic mutatednu- cleophosmin. Proc Natl Acad Sci USA, 2008, 105 (10) :3945 -3950.
  • 9Jonqen - Lavrencic M, Sun S M, Dijkstra M K, et al. MicroRNA expression profiling in relation to the genetic heterogeneity of acutemy- eloid leukemia. Blood, 2008, 111 (I0) :5078 - 5085.
  • 10Ramiro Garzon,Carlo M,Croce. MicroRNAs in normal and mallignant hematopoiesis. Current opinion in hematology,2008,15 (4) :352 - 358.

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  • 1刘荣梅,李凤兰,王淑菊,胡宝忠.mRNA差异显示技术研究进展[J].黑龙江农业科学,2007(1):86-89. 被引量:5
  • 2张旗,何湘君,潘秀英.RNA加尾和引物延伸RT-PCR法实时定量检测microRNA[J].北京大学学报(医学版),2007,39(1):87-91. 被引量:23
  • 3Ambros V. The functions of animal microRNAs[J]. Nature, 2004, 431(7006):350-355.
  • 4Bartel DP. MicroRNAs:genomics, biogenesis, mechanism, and function[J]. Cell, 2004, 116(2):281-297.
  • 5Plasterk RH. MicroRNAs in animal development[J]. Cell, 2006, 124(5):877-881.
  • 6Poy MN, Spranger M, Stoffel M. microRNAs and the regulation of glucose and lipid metabolism[J]. Diabetes Obes Metab, 2007, 2:67-73.
  • 7Chert CZ. MicroRNAs as oncogenes and tumor suppressors [J]. N Engl J Med, 2005, 353(17):1768-1771.
  • 8Kano M, Seki N, Kikkawa N, et al. miR-145, miR-133a and miR-133b:Tumor suppressive miRNAs target FSCN1 in esophageal squamous cell carcinoma[J]. Int J Cancer Suppl, 2010, 127(12):2804-2814.
  • 9Chiyomaru T, Enokida H, Tatarano S, et al. miR-145 and miR-133a function as tumour suppressors and directly regu- late FSCN1 expression in bladder cancer[J]. Br J Cancer, 2010,102(5):883-891.
  • 10Uchida Y, Chiyomaru T, Enokida H, et al. MiR-133a induces apoptosis through direct regulation of GSTP1 in bladder cancer cell lines[J]. Urol Oncol, 2011, [Epub ahead of print].

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