Abstract | OBJECTIVE: METHODS: Train a large number of recombinant human HMGN2 expression vector Escherichia coli BL21. HMGN2 was expressed under isopropyl-1-thio-beta-galactopyranoside ( IPTG) induction and purified by B-PER GST Fusion Protein Purification Kit. A variety of concentrations HMGN2 were added to cell culture medium, cells were tested by MTT, Hoechst 33342 fluorescence staining, flow cytometry assay and Western-blot. RESULTS: MTT results proved that HMGN2 could significantly inhibit human oral squamous cell carcinoma Tca8113 growth. Hoechst 33342 fluorescence staining, flow cytometry assay test and Western-blot proved HMGN2 could make Tca8113 cells morphological change, make Tca8113 cells block in S period of cell cycle and strongly promote Tca8113 cells to apoptosis. CONCLUSION:
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Authors | Xiaoqian Dong, Xiqian Liu, Yonghong Zhang, Ping Zhang, Libing Lu, Xiaoyu Li, Ping Huang, Yun Feng |
Journal | Hua xi kou qiang yi xue za zhi = Huaxi kouqiang yixue zazhi = West China journal of stomatology
(Hua Xi Kou Qiang Yi Xue Za Zhi)
Vol. 31
Issue 1
Pg. 91-5
(Feb 2013)
ISSN: 1000-1182 [Print] China |
PMID | 23484311
(Publication Type: Journal Article)
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Chemical References |
- High Mobility Group Proteins
- Recombinant Proteins
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Topics |
- Apoptosis
- Carcinoma, Squamous Cell
- Cell Proliferation
- High Mobility Group Proteins
- Humans
- In Vitro Techniques
- Mouth Neoplasms
- Recombinant Proteins
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