首页> 外文期刊>Technology in cancer research & treatment. >Long Noncoding RNA Maternally Expressed Gene 3 Is Downregulated, and Its Insufficiency Correlates With Poor-Risk Stratification, Worse Treatment Response, as Well as Unfavorable Survival Data in Patients With Acute Myeloid Leukemia
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Long Noncoding RNA Maternally Expressed Gene 3 Is Downregulated, and Its Insufficiency Correlates With Poor-Risk Stratification, Worse Treatment Response, as Well as Unfavorable Survival Data in Patients With Acute Myeloid Leukemia

机译:长度非编码RNA母体表达基因3是下调的,其功能不全与风险差的分层,较差的治疗反应以及急性髓性白血病患者的不利存活数据相关

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Objective: Our study aimed to investigate the correlation of long noncoding RNA maternally expressed gene 3 expression with clinical features, treatment response, and survival profiles in patients with acute myeloid leukemia. Methods: Bone marrow samples of 122 de novo patients with acute myeloid leukemia (prior to treatment) and 30 healthy donors (after enrollment) were collected, and long noncoding RNA maternally expressed gene 3 expression was detected by reverse transcription quantitative polymerase chain reaction. According to median value of long noncoding RNA maternally expressed gene 3 expression in patients with acute myeloid leukemia, they were divided into long noncoding RNA maternally expressed gene 3 high expression and low expression patients (which were further categorized as low---, low--, and low- expression patients). Results: Long noncoding RNA maternally expressed gene 3 expression was decreased in patients with acute myeloid leukemia compared to healthy donors. Besides, receiver operating characteristic curve displayed that long noncoding RNA maternally expressed gene 3 distinguished patients with acute myeloid leukemia from healthy donors. In patients with acute myeloid leukemia, long noncoding RNA maternally expressed gene 3 low expression was associated with poor-risk stratification but was not correlated with age, gender, French-American-Britain classification, or white blood cell level. For prognosis, complete remission rate was lowest in long noncoding RNA maternally expressed gene 3 low--- expression patients, followed by long noncoding RNA maternally expressed gene 3 low-- expression patients, long noncoding RNA maternally expressed gene 3 low- expression patients, and was highest in long noncoding RNA maternally expressed gene 3 high expression patients; Kaplan-Meier curves displayed that lower long noncoding RNA maternally expressed gene 3 expression was associated with reduced event-free survival and overall survival; Cox regression analysis showed that lower long noncoding RNA maternally expressed gene 3 expression independently predicted decreased event-free survival and worse overall survival in patients with acute myeloid leukemia. Conclusion: Long noncoding RNA maternally expressed gene 3 may function as a novel marker for effective surveillance and management of acute myeloid leukemia.
机译:目的:我们的研究旨在探讨长的非分量RNA母体表达基因3表达与临床特征,治疗反应和急性髓性白血病患者的存活谱的相关性的相关性。方法:122 de Novo患者急性髓性白血病(治疗前)和30次健康供体(在注册后)骨髓样品,通过逆转录定量聚合酶链反应检测长的非分量RNA母物表达基因3表达。根据长的非致RNA母体表达基因3患者的中位值,急性髓性白血病患者的表达,它们分为长度非编码RNA母体表达基因3高表达和低表达患者(其进一步分类为低---,低 - - 和低表达患者)。结果:与健康供体相比,急性髓性白血病患者的急性髓性白血病患者减少了长时间的RNA母体表达基因3表达。此外,接收器操作特征曲线显示,长度非编码RNA母体表达基因3患有来自健康供体的急性髓性白血病的患者。在急性髓性白血病患者中,长的非编码RNA母体表达基因3低表达与风险差,但与年龄,性别,法国 - 英国分类或白细胞水平无关。对于预后,长度非编码RNA母物表达基因3低---表达患者的完全缓解率最低,其次是长的非编码RNA母体表达基因3低 - 表达患者,长的非编码RNA母物表达基因3低表达患者,在长度非编码RNA母体表达基因3个高表达患者中最高; Kaplan-Meier曲线显示,低长度的无量化RNA母体表达基因3表达与无畸形生存和整体存活率降低有关; Cox回归分析表明,较低的长度非编码RNA母体表达基因3表达,独立预测的急性髓性白血病患者的无前活存活率和更差的整体存活率下降。结论:长度非编码RNA母体表达基因3可用作新型标志物,用于有效监测和管理急性髓性白血病。

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