评估分化拮抗非蛋白编码RNA (DANCR)在新诊断的埃及急性髓性白血病患者中的表达

IF 1 Q3 MEDICINE, GENERAL & INTERNAL
Nour Mohammed Rasheed, Howaida Attia Nounou, Soad Mohamed Eltabakh, Nahla A. M. Hamed, Ayman Ahmed Darwish
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引用次数: 0

摘要

近年来,长链非编码rna在癌症研究中的作用越来越突出,有证据表明它们参与了癌症的发病和进展。这些新兴的长链非编码RNA之一是分化拮抗非蛋白编码RNA (DANCR)。DANCR在不同肿瘤中的独特表达及其与肿瘤信号通路的关系使其成为一种有前景的肿瘤治疗靶点。本研究的目的是评估新发急性髓性白血病(AML)患者的DANCR表达,评估DANCR表达与细胞遗传学和法、美、英(FAB) AML分类的关系,以及DANCR表达与患者治疗反应的相关性。本研究包括60名新诊断的AML患者和30名健康受试者作为对照。采用实时荧光定量pcr法进行DANCR的相对表达。结果AML患者与对照组相比,DANCR显著下调(p = 0.038)。此外,与M0、M1和M2组相比,M4和M5中DANCR的表达显著降低(p <0.001)。此外,与对照组相比,细胞遗传学正常的AML患者的DANCR表达显著下调(p = 0.011)。结论AML中DANCR的显著下调提示其具有潜在的抑瘤作用,而不同AML亚型间DANCR表达的差异提示不同AML亚型间DANCR的作用可能不同。此外,具有较高DANCR表达的M1亚型患者对治疗的难治性较低,因此对阿糖胞苷的耐药性较低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Assessing the expression of differentiation antagonizing non-protein coding RNA (DANCR) in newly diagnosed Egyptian acute myeloid leukemia patients
Abstract Background Role of Long non-coding RNAs in cancer research in the recent years have been highlighted with evidence to their involvement in cancer disease pathogenesis and progression. One of these emerging long non-coding RNAs is differentiation antagonizing non-protein coding RNA (DANCR). DANCR distinct expression in different cancers and implication in tumor signaling pathways made it a promising therapeutic target for cancer. The purpose of this study was to evaluate DANCR expression in de novo acute myeloid leukemia (AML) patients and to assess DANCR expression in relation to cytogenetics and French American British (FAB) AML classification as well as correlate DANCR expression with patients’ response to treatment. The present study included 60 newly diagnosed AML patients and 30 healthy subjects as controls. Relative DANCR expression was done using real time qPCR method. Results DANCR was significantly downregulated in AML patients compared to controls ( p = 0.038). In addition, DANCR showed significantly lower expression in M4 and M5 compared to M0, M1, and M2 groups ( p < 0.001). Furthermore, DANCR expression was significantly downregulated in cytogenetically normal AML patients compared to the controls ( p = 0.011). Conclusion Significant downregulation of DANCR in AML suggests a potential tumor suppressor role and variable expression of DANCR among AML subtypes suggests that DANCR action may be different among AML subtypes. Also, M1 subtype patients with higher DANCR expression were less refractory to treatment and therefore less resistant to cytarabine.
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