Effects of disulfiram on apoptosis in PANC-1 human pancreatic cancer cell line

被引:1
|
作者
Dastjerdi, M. Nikbakht [1 ]
Babazadeh, Z. [1 ]
Rabbani, M. [2 ]
Gharagozloo, M. [3 ]
Esmaeili, A. [4 ]
Narimani, M. [5 ]
机构
[1] Isfahan Univ Med Sci, Med Sch, Dept Anat Sci & Mol Biol, Esfahan, Iran
[2] Isfahan Univ Med Sci, Sch Pharm & Pharmaceut Sci, Dept Pharmacol, Esfahan, Iran
[3] Isfahan Univ Med Sci, Med Sch, Dept Immunol, Esfahan, Iran
[4] Univ Isfahan, Fac Sci, Dept Biol, Cell Mol & Dev Biol Div, Esfahan, Iran
[5] Kurdistan Univ Med Sci, Sch Med, Mol Med, Kurdistan, Iran
关键词
Disulfiram; Human pancreatic cancerous cell line (PANC-1); Appotosis; RASSF1A; p21; Bax;
D O I
暂无
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Pancreatic carcinoma is currently considered as a rapidly progressive and fatal disease, and is typically diagnosed late in its natural course. It is characterized by a poor diagnosis and lack of response to conventional therapy. Recent studies have suggested that disulfiram (DSF), a member of the dithiocarbamate family, may have antitumor activity. This study aimed to evaluate the in vitro effect of DSF on apoptosis in human pancreatic cancerous cell line (PANC-1). PANC-1 cells were cultured and treated with DSF at doses of 5, 10, 13 mu M for 24 h and apoptosis was measured. Methylation specific PCR (MS-PCR) and real-time quantitative PCR were carried out to detect the methylation pattern and to estimate the mRNA expression levels of RASSF1A, p21 and Bax. MS-PCR analysis demonstrated that no unmethylated band was apeared in PANC-1 cell line after DSF treatments. The real-time quantitative PCR results showed no significant mRNA expression for RASSF1A (p>0.05); whereas p21 and Bax expression were significantly (p<0.01) enhanced after treatment with DSF. The results of the current study indicated that DSF can induce appoptosis in PANC-1 through p21 and Bax pathway but not through RASSF1A.
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页码:287 / 294
页数:8
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