高级搜索
肝癌细胞自噬性凋亡过程中caspase-3基因的克隆与鉴定[J]. 肿瘤防治研究, 2006, 33(05): 349-351. DOI: 10.3971/j.issn.1000-8578.2897
引用本文: 肝癌细胞自噬性凋亡过程中caspase-3基因的克隆与鉴定[J]. 肿瘤防治研究, 2006, 33(05): 349-351. DOI: 10.3971/j.issn.1000-8578.2897
Cloning and Identification of Caspase-3 Gene from HepG2 Cells that Underwent Autophagic Apoptosis[J]. Cancer Research on Prevention and Treatment, 2006, 33(05): 349-351. DOI: 10.3971/j.issn.1000-8578.2897
Citation: Cloning and Identification of Caspase-3 Gene from HepG2 Cells that Underwent Autophagic Apoptosis[J]. Cancer Research on Prevention and Treatment, 2006, 33(05): 349-351. DOI: 10.3971/j.issn.1000-8578.2897

肝癌细胞自噬性凋亡过程中caspase-3基因的克隆与鉴定

Cloning and Identification of Caspase-3 Gene from HepG2 Cells that Underwent Autophagic Apoptosis

  • 摘要: 目的从长春新碱诱导发生自噬性凋亡的肝癌细胞系HepG2中克隆caspase-3基因。方法提取细胞总RNA,采用RT-PCR技术扩增目的片段,构建重组克隆载体,测序鉴定及分析。结果经RT-PCR获得了预期的扩增产物即caspase-3基因625bp的核苷酸片段,其测序结果与文献报道一致。结论初步证明该caspase-3基因片段参与了长春新碱诱导的HepG2细胞自噬性凋亡过程。

     

    Abstract: Objective To acquire the fragment of caspase-3 gene from HepG2 cells, a human hepatocarcinoma cell line,that underwent autophagic apoptosis induced by vincristine(VCR). Methods Total RNA was extracted from the HepG2 cell line,then the fragment of caspase-3 gene from the cells was amplified by RT-PCR and it was cloned,sequenced by gene recombination techniques for confirmation. Results The prospective sequence of selected cloned caspase-3 gene was 625 bp.It is consistent with that of reported human caspase-3 g...

     

/

返回文章
返回