2021•PubMedRequires access

[Knockdown of Aurora-A inhibits proliferation and promotes apoptosis of HepG2 hepatocellular carcinoma cells].

Zhongxian Li, Shuxia Han, Bin Liu, Wenping Bu, Di Liu, Hui Yan, Qing Liu

Open publisher page 2 citations

Abstract

Objective To investigate the effects of knockdown of Aurora-A gene on the proliferation and apoptosis of HepG2 human hepatocellular carcinoma cells. Methods Aurora-A short hairpin RNA (Aurora-A shRNA) was designed and Aurora-A shRNA lentiviral vector was constructed and packed, and then transfected into HepG2 cells. Aurora-A mRNA expression was detected by real-time quantitative PCR. Aurora-A protein expression and phosphorylation level were detected by Western blotting. Cell proliferation was tested by MTT assay. Cell apoptosis was analyzed by flow cytometry. Results The Aurora-A shRNA lentiviral vector was successfully constructed and Aurora-A protein phosphorylation level was significantly reduced in HepG2 cells transfected with the lentiviral vector. When Aurora-a was knocked down, the proliferation of HepG2 cells decreased and the apoptosis rate increased significantly. Conclusion Knockdown of Aurora-A can inhibit the proliferation and promote the apoptosis of HepG2 cells.

About this research paper

What this paper is about

Objective To investigate the effects of knockdown of Aurora-A gene on the proliferation and apoptosis of HepG2 human hepatocellular carcinoma cells. Methods Aurora-A short hairpin RNA (Aurora-A shRNA) was designed and Aurora-A shRNA lentiviral vector was constructed and packed, and then transfected into HepG2 cells. Aurora-A mRNA expression was detected by real-time quantitative PCR. Aurora-A protein expression and phosphorylation level were detected by Western blotting. Cell proliferation was tested by MTT assay. Cell apoptosis was analyzed by flow cytometry. Results The Aurora-A shRNA lentiviral vector was successfully constructed and Aurora-A protein phosphorylation level was significantly reduced in HepG2 cells transfected with the lentiviral vector. When Aurora-a was knocked down, the proliferation of HepG2 cells decreased and the apoptosis rate increased significantly. Conclusion Knockdown of Aurora-A can inhibit the proliferation and promote the apoptosis of HepG2 cells.

Why it matters

OpenAlex reports 2 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Objective To investigate the effects of knockdown of Aurora-A gene on the proliferation and apoptosis of HepG2 human hepatocellular carcinoma cells. Methods Aurora-A short hairpin RNA (Aurora-A shRNA) was designed and Aurora-A shRNA lentiviral vector was constructed and packed, and then transfected into HepG2 cells. Aurora-A mRNA expression was detected by real-time quantitative PCR. Aurora-A protein expression and phosphorylation level were detected by Western blotting. Cell proliferation was tested by MTT assay. Cell apoptosis was analyzed by flow cytometry. Results The Aurora-A shRNA lentiviral vector was successfully constructed and Aurora-A protein phosphorylation level was significantly reduced in HepG2 cells transfected with the lentiviral vector. When Aurora-a was knocked down, the proliferation of HepG2 cells decreased and the apoptosis rate increased significantly. Conclusion Knockdown of Aurora-A can inhibit the proliferation and promote the apoptosis of HepG2 cells.

Key concepts: Small hairpin RNA, Gene knockdown, Transfection, Apoptosis, Flow cytometry, Cell growth, Blot, Molecular biology

Related papers

Back to paper searchBrowse research topicsOriginal source
[Knockdown of Aurora-A inhibits proliferation and promotes apoptosis of HepG2 hepatocellular carcinoma cells]. — Research Paper | ScholarLens