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Expression pattern and prognostic implication of SALL4 gene in myeloid leukemias: a case-control study

机译:Sall4基因在骨髓白血病中的表达模式及预后意蕴:一个病例对照研究

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摘要

SALL4 is a transcription factor that retains stem cells in an undifferentiated state and promotes its self-renewal. In addition, it is implicated in leukemogenesis via its effect on leukemic stem cells. This study aimed to characterize the expression pattern of SALL4 gene in acute myeloid leukemia (AML) and chronic myeloid leukemia (CML) at different progression phases of the leukemic process and to assess its prognostic significance. Real-time PCR was used in 106 patients: 54 AML patients; 43 de novo and 11 in complete remission (CR), 52 CML patients; 31 in chronic phase (CP), 11 in deep molecular response (MR4) and 10 in accelerated/blastic phase (AP/BP); and in 21 nonmalignant bone marrow samples. SALL4 gene expression was elevated in AML, AML-CR and CML-CP (median = 5.180, 4.604 and 14.125 fold changes, respectively). Elevated SALL4 gene expression among AML de novo patient was associated with poor disease-free survival (DFS) rates (p = .022). Among CML patients, the highest percentage of patients with a high SALL4 (p = .033) was among CML-CP. SALL4 has a role in leukemogenesis; high SALL4 expression was associated with poor DFS among AML patients.
机译:SALL4是一种转录因子,其在未分化状态下保留干细胞,并促进其自我更新。此外,它通过其对白血病干细胞的影响涉及白血病。该研究旨在在白血病过程的不同进展阶段表征急性髓性白血病(AML)和慢性骨髓白血病(CML)中SALL4基因的表达模式,评估其预后意义。实时PCR用于106例患者:54例AML患者; 43 de Novo和11在完全缓解(CR),52名CML患者中; 31在慢性相(CP),11的深分子响应(MR4)和10中的加速/弹性相(AP / BP);并且在21种非空种骨髓样品中。 SALL4基因表达在AML,AML-CR和CML-CP中升高(中位数= 5.180,4.604和14.125倍变化)。 AML de Novo患者中的升高的SALL4基因表达与无病的存活率(DFS)率差(P = .022)有关。在CML患者中,高张显示屏(P = .033)的患者的最高百分比是CML-CP。 Sall4在白血病中作用;高SALL4表达与AML患者之间的DFS差有关。

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