Abstract
Objective
Increasing evidence shows that microRNA (miR) is related to drug resistance in hepatocellular carcinoma (HCC). miR-34b-5p could retard tumor development, but its function in HCC is still unclear.
Methods
miR-34b-5p expression was determined in HCC tissues and cell lines. Analysis and verification of the binding between miR-34b-5p and metadherin (MTDH) was carried out. The actual action of miR-34b-5p and MTDH in the area of proliferation, apoptosis, invasion, and migration of cisplatin (DDP)-resistant HCC cells was monitored.
Results
miR-34b-5p was downregulated in HCC. Overexpression of miR-34b-5p enhanced the sensitivity of HCC cells to DDP, inhibiting proliferation, migration, and invasion and promoting apoptosis. MTDH was the direct target of miR-34b-5p. MTDH was upregulated in HCC tissues, which was negatively correlated with miR-34b-5p expression. Enhancement of MTDH can reverse the effect of upregulated miR-34b-5p on the chemosensitivity of HCC cells.
Conclusion
miR-34b-5p targets MTDH and enhances the chemosensitivity of HCC cells.
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Data availability
Data are available from the corresponding author on request.
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JC and LW designed the research study. XW and ZD performed the research. WC and LY provided help and advice. YZ, LX, and ZS analyzed the data. JC and LW wrote the manuscript. ZS reviewed and edited the manuscript. All authors contributed to editorial changes in the manuscript. All authors read and approved the final manuscript.
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JinSuo Chen, LiNa Wang, XueMei Wu, ZhiJie Ding, WenXi Cao, LeiLei Yang, YongPing Zhou, Li Xia, and Zhao Song have no conflicts of interest to declare.
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All procedures performed in this study involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards. All subjects was approved by Jiangnan University Medical Center (Approval number is JN2014-0832).
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Chen, J., Wang, L., Wu, X. et al. MicroRNA-34b-5p increases chemosensitivity of hepatocellular carcinoma cells. Mol. Cell. Toxicol. (2024). https://doi.org/10.1007/s13273-024-00431-z
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DOI: https://doi.org/10.1007/s13273-024-00431-z