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长链非编码 RNA 在急性髓系白血病中的临床相关性:系统评价与荟萃分析。

Clinical relevance of long non-coding RNA in acute myeloid leukemia: A systematic review with meta-analysis.

机构信息

Amity Institute of Biotechnology, Amity University, Gurugram, Haryana 122413, India.

Amity Institute of Molecular Medicine & Stem Cell Research (AIMMSCR), Amity University, Sector-125, Noida, Uttar Pradesh 201313, India.

出版信息

Leuk Res. 2024 Dec;147:107595. doi: 10.1016/j.leukres.2024.107595. Epub 2024 Sep 23.

Abstract

BACKGROUND

Long noncoding RNAs (lncRNAs) may function as prognostic biomarkers in acute myeloid leukaemia (AML). However, it is still unknown exactly how significant lncRNAs are for the prognosis of AML. With a focus on their prognostic and therapeutic potential, the study aimed to provide a comprehensive review of the literature regarding the role of lncRNAs in AML.

METHOD

Pub Med, The Cochrane Library, Embase, Science Direct, Web of science, Scopus, and Google scholar were searched until November, 2023. Original publications of any type exploring the prognostic and therapeutic potential of lncRNAs in AML patients were included. Heterogeneity and publication bias were examined using the I test and a funnel plot, respectively. To quantify the relationship between various lncRNA expression in AML patient survival, odds ratios (ORs) or hazards ratios (HRs) with 95 % confidence intervals (CIs) were pooled. Quality of studies was assessed using the Critical Appraisal Checklists for Studies created by the Joanna Briggs Institute (JBI).

RESULTS

Twenty-seven studies including 5665 subjects were selected for the final analysis. In patients with AML, abnormal lncRNA expression has been associated with significant worse overall survival (pooled HR = 2.05, 95 % CI = 1.79-2.30, P <0.001), shorter disease-free survival (pooled HR = 2.17, 95 % CI = 1.13-3.22, P< 0.001), and lower complete remission rate (pooled HR = 0.27, 95 % CI = 0.11-0.43, P< 0.001). Poor prognoses have been attributed to increased expression of HOX transcript antisense intergenic RNA (HOTAIR), Promoter Of CDKN1A Antisense DNA Damage Activated RNA (PANDAR), Metastasis Associated Lung Adenocarcinoma Transcript 1 (MALAT1), RP11-222K16.2, Taurine Upregulated Gene 1 (TUG1), Small Nucleolar RNA Host Gene 5 (SNHG5), Growth Arrest Specific 5 (GAS5), and H19 and decreased expression of IGF1R Antisense Imprinted Non-Protein Coding RNA (IRAIN).

CONCLUSION

The prognoses of AML patients are significantly associated with abnormally expressed lncRNAs, which may be used as prognostic indicators for predicting the patient outcomes.

摘要

背景

长链非编码 RNA(lncRNAs)可能在急性髓系白血病(AML)中作为预后生物标志物发挥作用。然而,lncRNAs 对 AML 预后的重要程度尚不清楚。本研究着眼于 lncRNAs 的预后和治疗潜力,旨在对 lncRNAs 在 AML 中的作用进行全面的文献综述。

方法

检索 Pub Med、The Cochrane Library、Embase、Science Direct、Web of science、Scopus 和 Google scholar,检索时间截至 2023 年 11 月。纳入任何类型的探讨 AML 患者 lncRNAs 预后和治疗潜力的原始文献。使用 I 检验和漏斗图分别检查异质性和发表偏倚。使用乔安娜布里格斯研究所(JBI)制定的批判性评估清单评估研究质量。使用 95%置信区间(CI)汇总的比值比(OR)或风险比(HR)来量化 AML 患者生存中各种 lncRNA 表达与生存率之间的关系。

结果

共纳入 27 项研究,包含 5665 例患者进行最终分析。在 AML 患者中,异常的 lncRNA 表达与总生存期显著更差相关(合并 HR=2.05,95%CI=1.79-2.30,P<0.001),无病生存期更短(合并 HR=2.17,95%CI=1.13-3.22,P<0.001),完全缓解率更低(合并 HR=0.27,95%CI=0.11-0.43,P<0.001)。HOX 转录物反义基因间 RNA(HOTAIR)、CDKN1A 反义 DNA 损伤激活 RNA(PANDAR)、肺腺癌转移相关转录物 1(MALAT1)、RP11-222K16.2、牛磺酸上调基因 1(TUG1)、小核仁 RNA 宿主基因 5(SNHG5)、生长停滞特异性基因 5(GAS5)和 H19 的表达增加以及 IGF1R 反义印记非蛋白编码 RNA(IRAIN)的表达降低与不良预后相关。

结论

AML 患者的预后与异常表达的 lncRNAs 显著相关,这些 lncRNAs 可能作为预测患者结局的预后指标。

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