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Cenp-E表达下调与HepG-2细胞染色体数目异常的关系研究

刘斌 刘卓然 翁亚光 刘子杰 蔡燕

重庆医学2011,Vol.40Issue(33):3340-3341,3345,3.
重庆医学2011,Vol.40Issue(33):3340-3341,3345,3.DOI:10.3969/j.issn.1671-8348.2011.33.004

Cenp-E表达下调与HepG-2细胞染色体数目异常的关系研究

Study on the relationship between the low expression of Cenp-E and chromosome numerical abnormality in HepG-2

刘斌 1刘卓然 1翁亚光 2刘子杰 2蔡燕2

作者信息

  • 1. 南华大学附属第二医院,湖南衡阳,421001
  • 2. 重庆医科大学检验系,400016
  • 折叠

摘要

Abstract

Objective To study the role and localization of Cenp-E gene in HepG-2 cell. Methods The cell cycle changes of HepG-2 cell and LO2 cell synchronized by nocodazole were detected by flow cytometry. The chromosome assay was uesd to detected the number and karyotype of chromosome of HepG-2 cell and LO2 cell. Cenp-E mRNA expressions in HepG-2 cell and LO2 cell synchronized by nocodazole were detected by RFQ-PCR. In the mean while. Cenp-E protein localization and expressions in HepG-2 cell and LO2 cell were oberved by indirect immunofluorescence. In the end,RNAi technology was used to further evaluated the function of Cenp-E in LO2 cell. Results HepG-2 cell and LO2 cell were arrested in G2/M phase synchronized by nocodazole. The chromosome assay showed that the proportion of abnormal chromosomes cell in HepG-2 cell were higher then LO2 cell. After synchronized by nocodazole,Cenp-E mRNA and protein expressions of HepG-2 cell was higher then LO2 cell. Cenp-E mRNA and protein expressions of LO2 cell decreased significantly. Conclusion The low expression of Cenp-E may be one of the important reasons of chromosome numerical abnormality in human hepatoma cells.

关键词

肝肿瘤/染色体/纺锤体检查点蛋白E

Key words

liver neoplasms/ chromosomes/ spindle checkpoint proteinE

引用本文复制引用

刘斌,刘卓然,翁亚光,刘子杰,蔡燕..Cenp-E表达下调与HepG-2细胞染色体数目异常的关系研究[J].重庆医学,2011,40(33):3340-3341,3345,3.

重庆医学

OA北大核心CSCDCSTPCD

1671-8348

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