E-ISSN: 1308-5263
miR-379-5p Inhibited the Proliferation of Acute Myeloid Leukemia Cells Through Negative Regulation of YBX1 [Turk J Hematol]
Turk J Hematol. 2025; 42(2): 92-99 | DOI: 10.4274/tjh.galenos.2025.2024.0424

miR-379-5p Inhibited the Proliferation of Acute Myeloid Leukemia Cells Through Negative Regulation of YBX1

Huichao Wu1, Lin Zhao2, Huanyu Guo3, Yingjie Xie4, Jianhua Hu5, Xinxia Tan6
1The First People’s Hospital of Jiashan, Department of Emergency, Jiashan, P.R. China
2Dongzhimen Hospital, Beijing University of Chinese Medicine, Department of Hematology and Oncology, Beijing, P.R. China
3Changchun University of Chinese Medicine, Faculty of Clinical Medicine, Changchun, P.R. China
4General Hospital of Southern Theater Command of the Chinese PLA, Departments of Cadre Ward, Guangzhou, P.R. China
5People’s Hospital of Quzhou, Department of Intensive Care Medicine, Quzhou, P.R. China
6Huangshi Central Hospital (Affiliated Hospital of Hubei Polytechnic University), Department of Clinical Laboratory, Huangshi, P.R. China; Huangshi Tumor Molecular Diagnosis and Treatment Key Laboratory, Huangshi, P.R. China

Objective: Acute myeloid leukemia (AML) highly lethal hematological malignancy that is difficult to treat. This study aimed to clarify the molecular mechanisms of miR-379-5p in AML progression.
Materials and Methods: Quantitative real-time polymerase chain reaction was utilized to evaluate miR-379-5p expression levels in AML patients and a control group. A receiver operating characteristic curve was created to assess the clinical predictive value of miR-379-5p in AML, while cell experiments used the CCK-8 assay, flow cytometry, and transwell chambers. Potential target genes of miR-379-5p were predicted by employing online bioinformatics tools, followed by validation using a dual luciferase reporter assay.
Results: miR-379-5p expression was significantly decreased in AML patients and had clinical predictive value for the disease. In AML cell lines, miR-379-5p was downregulated; conversely, the upregulation of miR-379-5p inhibited proliferation, migration, and invasion while promoting apoptosis. Notably, YBX1 was a potential target gene of miR-379-5p and its upregulation reduced the effects of miR-379-5p on AML cell behavior.
Conclusion: miR-379-5p has potential as a biomarker for AML by regulating cell proliferation and apoptosis through the targeting of YBX1.

Keywords: Acute myeloid leukemia, miR-379-5p, YBX1, Cell proliferation, Apoptosis, Diagnostic significance

miR-379-5p YBX1 Negatif Düzenlemesi Aracılığı ile Akut Miyeloid Lösemi Hücrelerinde Proliferasyonu İnhibe Etti

Huichao Wu1, Lin Zhao2, Huanyu Guo3, Yingjie Xie4, Jianhua Hu5, Xinxia Tan6
1The First People’s Hospital of Jiashan, Department of Emergency, Jiashan, P.R. China
2Dongzhimen Hospital, Beijing University of Chinese Medicine, Department of Hematology and Oncology, Beijing, P.R. China
3Changchun University of Chinese Medicine, Faculty of Clinical Medicine, Changchun, P.R. China
4General Hospital of Southern Theater Command of the Chinese PLA, Departments of Cadre Ward, Guangzhou, P.R. China
5People’s Hospital of Quzhou, Department of Intensive Care Medicine, Quzhou, P.R. China
6Huangshi Central Hospital (Affiliated Hospital of Hubei Polytechnic University), Department of Clinical Laboratory, Huangshi, P.R. China; Huangshi Tumor Molecular Diagnosis and Treatment Key Laboratory, Huangshi, P.R. China

Amaç: Akut miyeloid lösemi (AML) tedavisi zor olan ve oldukça ölümcül bir hematolojik malignitedir. Bu çalışmada AML progresyonunda miR- 379-5p nin moleküler mekanizmalarını netleştirmeyi hedefledik.
Gereç ve Yöntem: AML hastaları ve kontrol grup örneklerinde kantitatif gerçek zamanlı polimeraz zincir reaksiyonu kullanılarak miR- 379-5p ekspresyon düzeyleri değerlendirildi. AML’de klinik prediktif miR-379-5p değerini ortaya çıkarabilmek için alıcı taraflı karakteristik bir eğri oluşturuldu. Hücre deneyleri ise CCK-8, akım sitometri ve transwell migrasyon tetkikini kullandı. miR-379-5p’nin potansiyel hedefleri online biyoinformatik tahmin araçları ile öngörülmüştür, peşinden dual lusiferaz raportör yöntemi ile doğrulanmıştır.
Bulgular: AML hastalarında miR-379-5p ekspresyonu belirgin şekilde azalmıştır ve hastalık için klinik prediktif değeri olduğu görülmüştür. AML hücre dizelerinde miR-379-5p azalmıştır, oysa ki artmış düzeyleri proliferasyonu, migrasyonu ve invazyonu inhibe ederek apopitozu tetikler. Özellikle YBX1 miR-379-5p geni potansiyel hedefidir ve artmış seviyeleri miR-379-5p nin AML hücre davranışındaki etkilerini azaltmaktadır.
Sonuç: miR-379-5p YBX1’i hedef alarak hücre proliferasyonu ve apopitozisin düzenlenmesi üzerinden AML için potansiyel bir biyobelirteç olabilir.

Anahtar Kelimeler: Akut miyeloid lösemi, miR-379-5p, YBX1, Hücre proliferasyonu, Apopitozis, Tanısal önem

Corresponding Author: Xinxia Tan
Manuscript Language: English
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