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Updated: Dec 24, 2025

Analysis of Combinatorial miRNA Treatments to Regulate Cell Cycle and Angiogenesis
Published on: March 30, 2019
MicroRNA-1271-5p inhibits cell proliferation and enhances radiosensitivity by targeting CDK1 in hepatocellular
Hong-Mei Liu1,2, Hua-Yan Tan2, Yue Lin1
1Research Department, Affiliated Cancer Hospital of Guangxi Medical University and Cancer Institute of Guangxi Zhuang Autonomous Region, Nanning, Guangxi 530021, P.R. China.
Abstract:
This study aims to determine whether miR-1271-5p inhibits cell proliferation and enhances the radiosensitivity by targeting cyclin-dependent kinase 1 (CDK1) in hepatocellular carcinoma (HCC). Its expression levels in the HCC cell lines were significantly lower than those in normal human liver cell line. Bioinformatics analysis indicated CDK1 was a potential target of miR-1271-5p. Dual-Luciferase Reporter Assay confirmed that CDK1 is a direct target gene of miR-1271-5p. With overexpression of miR-1271-5p in SMMC-7721 and HuH-7 cells, cell proliferation was decreased, radiosensitivity was enhanced, cell cycle distribution was altered and the growth of transplanted tumours in nude mice was significantly reduced. miR-1271-5p overexpression enhanced radiosensitivity, which could be reduced by CDK1 overexpression. Overall, our findings suggested that miR-1271-5p inhibits cell proliferation and enhances the radiosensitivity of HCC cell lines by targeting CDK1.
Insights
MicroRNA-1271-5p (miR-1271-5p) inhibits hepatocellular carcinoma (HCC) cell proliferation and improves radiosensitivity by targeting cyclin-dependent kinase 1 (CDK1). This finding offers a potential therapeutic strategy for HCC treatment.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Hepatocellular carcinoma (HCC) remains a significant global health challenge.
- Understanding the molecular mechanisms underlying HCC progression and treatment resistance is crucial.
- MicroRNAs (miRNAs) have emerged as key regulators in various cancers, including HCC.
Purpose of the Study:
- To investigate the role of miR-1271-5p in hepatocellular carcinoma (HCC).
- To determine if miR-1271-5p inhibits HCC cell proliferation and enhances radiosensitivity.
- To identify the direct molecular target of miR-1271-5p in HCC.
Main Methods:
- Bioinformatics analysis to predict potential miRNA targets.
- Dual-Luciferase Reporter Assay to validate direct miRNA-target interaction.
- In vitro cell culture experiments (SMMC-7721 and HuH-7 cells) to assess proliferation and radiosensitivity.
- In vivo studies using transplanted tumors in nude mice.
Main Results:
- miR-1271-5p expression was significantly lower in HCC cell lines compared to normal liver cells.
- Cyclin-dependent kinase 1 (CDK1) was identified as a direct target of miR-1271-5p.
- Overexpression of miR-1271-5p reduced HCC cell proliferation, enhanced radiosensitivity, altered cell cycle, and inhibited tumor growth in vivo.
- Restoring CDK1 expression attenuated the radiosensitizing effect of miR-1271-5p.
Conclusions:
- miR-1271-5p functions as a tumor suppressor in hepatocellular carcinoma.
- The inhibitory effect of miR-1271-5p on proliferation and its radiosensitizing properties are mediated through the targeting of CDK1.
- miR-1271-5p represents a potential therapeutic target for improving HCC treatment outcomes.
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