Jia Wang,
Hong Kou,
Ting Kong,
Wei Lu
Department of Children's Institute, Three Gorges University Yichang Central People's Hospital, The First College of Clinical Medical Sciences, Three Gorges University, Yichang 443003, Hubei Province, China;
For correspondence:- Wei Lu
Email: hanrong974293@163.com
Accepted: 6 May 2024
Published: 29 May 2024
Citation:
Wang J, Kou H, Kong T, Lu W.
Mir-204 regulates the biological behavior of childhood leukemia cells by binding to 3'UTR end of target gene and reducing the level of the gene. Trop J Pharm Res 2024; 23(5):801-808
doi:
10.4314/tjpr.v23i5.1
© 2024 The authors.
This is an Open Access article that uses a funding model which does not charge readers or their institutions for access and distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) and the Budapest Open Access Initiative (http://www.budapestopenaccessinitiative.org/read), which permit unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited..
Abstract
Purpose: To study the regulatory impact of mir-204 on the biological behavior of childhood leukemia cells and to elucidate its mechanism of action.
Methods: A total of 112 children with leukemia who were treated in Three Gorges University Yichang Central People's Hospital, Yichang, China from July 2018 to June 2020 were randomly divided into study and control groups (n = 56 each). The expression levels of mir-204 and hepatocyte growth factor (HGF) were determined using real-time polymerase chain chain reaction (RT-PCR) while the cell proliferation potential was determined using the CCK-8 method. Apoptosis and cell cycle progression of each group were evaluated using flow cytometry while changes in cell invasion and migration were assessed by Transwell assay. Luciferase reporter assay was used to determine the binding of mir-204 and HGF to 3'UTR.
Results: The expression level of mir-204 in study group was significantly lower than that in control group, while expression level of HGF was significantly higher (p < 0.01) compared to control group. There was no significant change in cell proliferation capacity at 24 h. The expression level of mir-204 was significantly decreased, while the expression level of HGF was significantly increased (p < 0.05). Luciferase activity of wild-type HGF 3'UTR in mir-204 overexpression group was significantly decreased, relative to mir-204 negative control group (p < 0.01). There was no significant difference in luciferase activity in mutant HGF gene between the two groups (p > 0.05).
Conclusion: Mir-204 reduces HGF expression level via HGF 3'UTR end, thereby inhibiting cell proliferation, invasion and migration, while promoting apoptosis, blocking cell cycle and regulating biological behavior of childhood leukemia cells.
Keywords: miR-204, Target gene, Leukemic cells in children, Biological behavior