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微小RNA-21表达作为慢性髓性白血病患者的预后和治疗反应标志物

microRNA-21 Expression as Prognostic and Therapeutic Response Marker in Chronic Myeloid Leukaemia Patients.

作者信息

Mirza Masroor Ali Beg, Guru Sameer Ahmad, Abdullah Saleh Mohammed, Rizvi Aliya, Saxena Alpana

机构信息

Department of Toxicology, Jamia Hamdard University, New Delhi, India.

Department of Biochemistry, Maulana Azad Medical College, New Delhi, India.

出版信息

Asian Pac J Cancer Prev. 2019 Aug 1;20(8):2379-2383. doi: 10.31557/APJCP.2019.20.8.2379.

Abstract

Background: Chronic myeloid leukaemia (CML) is a myeloproliferative disorder categorized by malignant transformation of a single stem cell of hematopoietic cells. microRNAs (miRNAs) belong to transcription regulators in hematopoiesis and their altered expression associates with pathogenesis of CML. Aim: Current study aimed to access the miR-21 expression profile in CML patients and therapy response as well as its prognostic significance. Methods: 100 CML cases, 100 controls were included in study and miR-21 expression was analyzed. Overall 9.22 mean fold increased expression was observed in CML patients before treatment. Results: Patients with different CML phases such as chronic phase, accelerated phase and blast crisis showed 7.16, 10.30 and 13.20 fold increased expression respectively. Overall 3.57 mean fold expression was observed in imatinib treated patients suggested more than 5 fold decreased expression in CML patients. Prognostic significance was calculated and observed that miR-21 expression at 7.29 fold cutoff, 75% sensitivity and 50% specificity was observed (AUC=0.75, p<0.0001). Study observed miR-21 overexpression in CML patients as well as gradually increased expression with advancement of disease. Conclusion: miR-21 overexpression represented molecular prognostic marker and predictive tool enabling efficient monitoring of drug response and therapy outcomes in CML patients.

摘要

背景

慢性髓性白血病(CML)是一种骨髓增殖性疾病,其特征为造血细胞的单个干细胞发生恶性转化。微小RNA(miRNA)属于造血过程中的转录调节因子,其表达改变与CML的发病机制相关。目的:本研究旨在探讨CML患者中miR-21的表达谱、治疗反应及其预后意义。方法:本研究纳入100例CML患者和100例对照,分析miR-21的表达。CML患者治疗前平均表达增加9.22倍。结果:不同CML分期(如慢性期、加速期和急变期)的患者分别显示表达增加7.16、10.30和13.20倍。伊马替尼治疗的患者平均表达为3.57倍,提示CML患者表达下降超过5倍。计算预后意义,观察到miR-21表达在7.29倍临界值时,敏感性为75%,特异性为50%(AUC = 0.75,p < 0.0001)。研究观察到CML患者中miR-21过表达,且随着疾病进展表达逐渐增加。结论:miR-21过表达代表分子预后标志物和预测工具,可有效监测CML患者的药物反应和治疗结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba95/6852824/3c2f822e7818/APJCP-20-2379-g001.jpg

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