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miR-181a 和 miR-196b 在埃及儿科急性淋巴细胞白血病中的表达。

Expression of microRNA-181a and microRNA-196b in Egyptian Pediatric acute Lymphoblastic Leukemia.

机构信息

Department of Clinical Pathology, NCI, Cairo University, Cairo, Egypt.

Department of Pediatric Oncology, NCI, Cairo University, Cairo, Egypt.

出版信息

Asian Pac J Cancer Prev. 2020 Nov 1;21(11):3429-3434. doi: 10.31557/APJCP.2020.21.11.3429.

Abstract

BACKGROUND

Differential expression of miRNA provides important insights into pathogenesis of cancer including leukemia. Deregulation of microRNA may contribute to hematopoietic malignancies. In this study, we aimed to evaluate the role of miR-181a and miR-196b in acute lymphoblastic leukemia (ALL) and correlate their expression with clinical and laboratory data.

METHODS

The study was performed on bone marrow samples of 70 consecutive newly diagnosed pediatric (ALL) patients, of which 56 were evaluated for both miR-181a and miR-196b (all 70 for miR-181a) by real-time quantitative reverse transcriptase polymerase chain reaction (RT-qPCR). In addition, bone marrow from seven age and sex matched healthy controls derived from donors of bone marrow transplantation were assessed.

RESULTS

miR-181a expression was significantly up-regulated in ALL patients compared with healthy controls (p <0.001). However, miR-196b expression was significantly down-regulated in patients compared with healthy controls (p=0.038).

CONCLUSION

Our results suggest that miR-181a has an oncogenic, while miR-196b has a tumor suppressive role in pediatric ALL patients. A finding which demonstrate the potential role of these microRNAs in pathogenesis of pediatric ALL. Also, estimation of their expression level may provide a tool for confirmation of a diagnosis of childhood ALL and could be a possible predictor of early relapse.
.

摘要

背景

miRNA 的差异表达为癌症(包括白血病)的发病机制提供了重要的见解。microRNA 的失调可能导致造血恶性肿瘤。在这项研究中,我们旨在评估 miR-181a 和 miR-196b 在急性淋巴细胞白血病(ALL)中的作用,并将其表达与临床和实验室数据相关联。

方法

对 70 例连续新诊断的儿科 ALL 患者的骨髓样本进行了研究,其中 56 例通过实时定量逆转录聚合酶链反应(RT-qPCR)评估了 miR-181a 和 miR-196b 的表达情况(所有 70 例均评估了 miR-181a)。此外,还评估了来自骨髓移植供体的 7 名年龄和性别匹配的健康对照者的骨髓。

结果

与健康对照组相比,ALL 患者的 miR-181a 表达明显上调(p<0.001)。然而,与健康对照组相比,miR-196b 在患者中的表达明显下调(p=0.038)。

结论

我们的结果表明,miR-181a 具有致癌作用,而 miR-196b 在儿科 ALL 患者中具有肿瘤抑制作用。这一发现表明这些 microRNAs 在儿科 ALL 的发病机制中具有潜在作用。此外,估计其表达水平可能为确认儿童 ALL 的诊断提供一种工具,并可能成为早期复发的一个可能预测因子。

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