Affiliation:
1. Laboratory Medicine and Biotechnology Southern Medical University Guangzhou Guangdong Province People's Republic of China
2. Clinical Laboratory Suizhou Central Hospital Suizhou Hubei Province People's Republic of China
3. Department of Hematology, Nanfang Hospital Southern Medical University Guangzhou Guangdong Province People's Republic of China
Abstract
AbstractAcute myeloid leukemia (AML) is a deadly hematologic malignancy. In this study, miR‐361‐3p and BTG2 gene expression in AML blood and healthy specimens were analyzed using quantitative real‐time reverse transcription polymerase chain reaction. A significant negative correlation between miR‐361‐3p and BTG2 was observed. The cell viability and apoptosis were measured by CCK‐8 assay, EdU incorporation assay and flow cytometry. A dual‐luciferase reporter gene assay was performed to confirm the binding sequence between miR‐361‐3p and BTG2 messenger RNA 3ʹ‐untranslated region. 9s‐Hydroxyoctadecadienoic acid (9s‐HODE), a major active derivative of linoleic acid, reduced the viability and induced cell apoptosis of HL‐60 cells. Furthermore, the miR‐361‐3p mimics and siBTG2 reversed the above effects of 9s‐HODE. 9s‐HODE exerted an anti‐AML effect through, at least partly, regulating the miR‐361‐3p/BTG2 axis.
Subject
Health, Toxicology and Mutagenesis,Toxicology,Molecular Biology,Molecular Medicine,Biochemistry,General Medicine