|本期目录/Table of Contents|

PDCD4促进吉西他滨诱导胰腺癌细胞凋亡的实验研究

《现代肿瘤医学》[ISSN:1672-4992/CN:61-1415/R]

期数:
2019年20期
页码:
3571-3576
栏目:
论着(基础研究)
出版日期:
2019-09-08

文章信息/Info

Title:
PDCD4 promoted the apoptosis of pancreatic cancer cells induced by gemcitabine
作者:
余 伟1;?张志标2;?张能平1;?马 达1;?刘礼军1
1.汉川市人民医院普外科二科;2.急诊科,湖北 汉川 431600
Author(s):
Yu Wei1;?Zhang Zhibiao2;?Zhang Nengping1;?Ma Da1;?Liu Lijun1
1.Department of General Surgery;2.Department of Emergency,Hanchuan People's Hospital,Hubei Hanchuan 431600,China.
关键词:
胰腺癌细胞;?PDCD4;?吉西他滨;?凋亡
Keywords:
pancreatic cancer cell;?PDCD4;?gemcitabine;?apoptosis
分类号:
R735.9
DOI:
10.3969/j.issn.1672-4992.2019.20.006
文献标识码:
A
qq自动领红包软件:
目的:研究程序性细胞死亡因子4(programmed cell death 4,PDCD4)在吉西他滨诱导胰腺癌细胞凋亡中的作用。方法:用吉西他滨处理胰腺癌细胞PANC-1,荧光定量PCR和Western blot分别检测胰腺癌细胞中PDCD4的表达变化。PANC-1细胞感染PDCD4-pGC-Fu-GFP重组慢病毒和对照pGC-Fu-GFP重组慢病毒,荧光定量PCR和Western blot检测过表达效果。用吉西他滨处理过表达PDCD4的PANC-1细胞,MTT测定细胞增殖,克隆形成实验测定细胞克隆能力,流式细胞术测定细胞凋亡,Western blot检测细胞中剪切的Caspase-3(Cleaved Caspase-3)、剪切的Caspase-9(Cleaved Caspase-9)蛋白水平和胞浆、线粒体中细胞色素C(Cytochrome C)蛋白水平。结果:吉西他滨处理后的PANC-1细胞中PDCD4 mRNA和蛋白水平均明显升高。吉西他滨处理和过表达PDCD4的PANC-1细胞增殖、克隆形成能力明显降低,细胞凋亡率明显升高,细胞中Cleaved Caspase-3、Cleaved Caspase-9蛋白水平升高,胞浆中Cytochrome C蛋白水平也升高,线粒体中Cytochrome C蛋白水平降低。吉西他滨处理过表达PDCD4的PANC-1细胞增殖能力、克隆形成能力降低更多,细胞凋亡率更高,细胞中Cleaved Caspase-3、Cleaved Caspase-9蛋白水平也更高,胞浆中Cytochrome C蛋白水平更高,线粒体中Cytochrome C蛋白水平更低。结论:吉西他滨通过上调PDCD4表达水平激活线粒体途径诱导胰腺癌细胞凋亡。
Abstract:
Objective:To study the role of PDCD4 in the apoptosis of pancreatic cancer cells induced by gemcitabine.Methods:Treatment of pancreatic cancer cell PANC-1 with gemcitabine,Fluorescence quantitative PCR and Western blot were used to detect the expression of PDCD4 in pancreatic cancer cells.PANC-1 cells infected with PDCD4-pGC-Fu-GFP recombinant lentivirus and control pGC-Fu-GFP recombinant lentivirus,Fluorescent quantitative PCR and Western blot were used to detect the overexpression.The PANC-1 cells expressing PDCD4 were treated with gemcitabine.MTT assay cell proliferation,clone formation experiment were used to determine the cell clone ability.Cell apoptosis was measured by flow cytometry.The levels of Cleaved Caspase-3,Cleaved Caspase-9 protein and Cytochrome C protein in cytoplasm and mitochondria were detected by Western blot.Results:PDCD4 mRNA and protein levels in gemcitabine treated PANC-1 cells increased significantly.After gemcitabine treatment and over expression of PDCD4,the proliferation and colony formation ability of PANC-1 cells were significantly reduced,and the rate of apoptosis was significantly increased,and the level of Cleaved Caspase-3 and Cleaved Caspase-9 protein increased in cells,the level of Cytochrome C protein in the cytoplasm also increased,the levels of Cytochrome C protein in mitochondria decreased.Gemcitabine reduced the proliferation and clone formation ability of PANC-1 cells expressing PDCD4,and the rate of cell apoptosis was higher.The levels of Cleaved Caspase-3 and Cleaved Caspase-9 protein in cells were also higher.The level of Cytochrome C protein in the cytoplasm was higher,and the level of Cytochrome C protein in mitochondria was lower.Conclusion:Gemcitabine induces apoptosis of pancreatic cancer cells by up regulating the expression level of PDCD4 and activating mitochondrial pathway.

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备注/Memo

备注/Memo:
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更新日期/Last Update: 1900-01-01