吉西他滨
转染
小发夹RNA
胰腺癌
细胞培养
分子生物学
MTT法
免疫印迹
信使核糖核酸
化学
癌症研究
生物
内科学
癌症
医学
基因
生物化学
基因敲除
遗传学
作者
Tao Peng,Feng Zhou,Peng Yang,Chunyou Wang
出处
期刊:Chinese Journal of Hepatobiliary Surgery
日期:2012-06-28
卷期号:18 (06): 459-461
标识
DOI:10.3760/cma.j.issn.1007-8118.2012.06.019
摘要
Objective To explore the effects of AKT2 expression in pancreatic cancer cell line Panc-1 on the sensitivity towards to gemcitabine. Methods The expression vector pAKT2-shRNA was constructed and transfected into Panc-1 cells by lipofecton. The mRNA and protein expression levels of AKT2 were detected by RT-PCR and Western blot assays, respectively. The changes of gem- citabine sensitivity after shRNA were examined by the MTT assay. Results The mRNA and protein levels of AKT2 in Panc-1 cells were significantly decreased after the transfection, and the median inhi- bition concentration of gemcitabine against Panc-1 cells was reduced from (1.96±0.22) mg/L to (0.24±0.03) mg/L. The sensitivity of Panc-1 cells to gemcitabine was increased significantly after pAKT2-shRNA transfeetion. Conclusion The sensitivity of Panc-1 cells to gemcitabine could be en- hanced by pAKT2-shRNA.
Key words:
Pancreatic cancer; Gene; Gemcitabine
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