Hashem Jood, Alkhalaileh Lujain, Abushukair Hassan, Ayesh Mahmoud
Department of Medical Laboratory Sciences, Jordan University of Science and Technology, Irbid 22110, Jordan.
Faculty of Medicine, Jordan University of Science and Technology, Irbid 22110, Jordan.
Biomedicines. 2024 Aug 22;12(8):1924. doi: 10.3390/biomedicines12081924.
The dysregulation of miRNA expression has been shown to impact cellular physiology and tumorigenesis. Studies have reported several miRNA regulatory elements and pathways that play a significant role in the diagnosis, prognosis, and treatment of hematological malignancies. This is the first study to test the differential expression of miRNAs at crucial stages of the disease, specifically newly diagnosed, resistant to treatment, and remission. Circulating miRNAs extracted from the blood samples of 18 patients diagnosed with leukemia or lymphoma at different stages and 2 healthy controls were quantified by qPCR using a panel of 96 tumorigenic miRNAs. An enrichment analysis was performed to understand the mechanisms through which differential miRNA expression affects cellular and molecular functions. Significant upregulation of hsa-miR-1, hsa-miR-20a-5p, hsa-miR-23a-3p, hsa-miR-92b3p, and hsa-miR-196a-5p was detected among the different stages of leukemia and lymphoma. mir-1 and mir-196a-5p were upregulated in the remission stage of leukemia, while mir-20a-5p, mir-23a-3p, and mir-92b-3p were upregulated during the resistant stage of lymphoma. The enrichment analysis revealed these miRNAs' involvement in the RAS signaling pathway, TGF-β signaling, and apoptotic pathways, among others. This study highlights new biomarkers that could be used as potential targets for disease diagnosis, prognosis, and treatment, therefore enhancing personalized treatments and survival outcomes for patients.
已表明miRNA表达失调会影响细胞生理学和肿瘤发生。研究报告了几种在血液系统恶性肿瘤的诊断、预后和治疗中起重要作用的miRNA调控元件和途径。这是第一项在疾病关键阶段,特别是新诊断、治疗耐药和缓解阶段检测miRNA差异表达的研究。使用一组96种致瘤性miRNA,通过qPCR对从18例不同阶段诊断为白血病或淋巴瘤的患者及2名健康对照的血液样本中提取的循环miRNA进行定量。进行富集分析以了解差异miRNA表达影响细胞和分子功能的机制。在白血病和淋巴瘤的不同阶段检测到hsa-miR-1、hsa-miR-20a-5p、hsa-miR-23a-3p、hsa-miR-92b3p和hsa-miR-196a-5p显著上调。mir-1和mir-196a-5p在白血病缓解期上调,而mir-20a-5p、mir-23a-3p和mir-92b-3p在淋巴瘤耐药期上调。富集分析显示这些miRNA参与RAS信号通路、TGF-β信号通路和凋亡通路等。本研究突出了可作为疾病诊断、预后和治疗潜在靶点的新生物标志物,从而改善患者的个性化治疗和生存结果。