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首页> 外文期刊>Hematology. >An anti-apoptotic pattern correlates with multidrug resistance in acute myeloid leukemia patients: a comparative study of active caspase-3, cleaved PARPs, Bcl-2, Survivin and MDR1 gene.
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An anti-apoptotic pattern correlates with multidrug resistance in acute myeloid leukemia patients: a comparative study of active caspase-3, cleaved PARPs, Bcl-2, Survivin and MDR1 gene.

机译:抗凋亡模式与急性髓性白血病患者的多药耐药性相关:活性caspase-3,裂解的PARPs,Bcl-2,Survivin和MDR1基因的比较研究。

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摘要

Bone marrow samples of 17 acute myeloid leukemia (AML) patients were analyzed for apoptosis-related markers. The levels of active caspase-3 (aC-3), Bcl-2 and cleaved poly(ADP-ribose) polymerase (cPARP) were measured by flow cytometry and compared with survivin and MDR1 gene expression as defined by reverse transcriptase polymerase chain reaction (RT-PCR). The results showed heterogeneous patterns of intracellular levels of the studied proteins in AML patients: aC-3 (mean 34.6+/-52.5 U/ml), Bcl-2 (mean 3268.4+/-2055.2 U/ml), and cPARPs (mean 24.59+/-29.97 U/ml). Survivin and MDR1 genes were overexpressed in 9 and 10 patients, respectively. Patients with high levels of survivin mRNA showed significantly lower cPARPs (11.8+/-14.3 versus 53.9+/-31.9 U/ml P=0.005) and a tendency towards higher aC-3 (49.3+/-70.0 versus 18.1+/-9.9 U/ml), and MDR1 overexpression (7/9 patients versus 3/8 patients), as well as poorer therapeutic response and survival. Our data support the potential relevance of apoptosis-related markers in AML for further understanding the disease; however, the heterogeneity and complexity of molecular interactions warrants further prospective studies.
机译:分析了17例急性髓细胞性白血病(AML)患者的骨髓样本中与凋亡相关的标志物。通过流式细胞仪测量活性caspase-3(aC-3),Bcl-2和裂解的聚(ADP-核糖)聚合酶(cPARP)的水平,并与逆转录酶聚合酶链反应定义的survivin和MDR1基因表达进行比较( RT-PCR)。结果显示AML患者中研究蛋白的细胞内水平存在异质性模式:aC-3(平均34.6 +/- 52.5 U / ml),Bcl-2(平均3268.4 +/- 2055.2 U / ml)和cPARPs(平均24.59 +/- 29.97 U / ml)。 Survivin和MDR1基因分别在9和10位患者中过表达。 survivin mRNA高水平的患者显示出较低的cPARPs(11.8 +/- 14.3对53.9 +/- 31.9 U / ml P = 0.005)和aC-3升高的趋势(49.3 +/- 70.0对18.1 +/- 9.9 U / ml)和MDR1过表达(7/9患者与3/8患者),以及较差的治疗反应和生存率。我们的数据支持AML中凋亡相关标记物与进一步了解疾病的潜在相关性。然而,分子相互作用的异质性和复杂性值得进一步的前瞻性研究。

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