Abstract
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 μM 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.
Original language | English (US) |
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Pages (from-to) | 287-294 |
Number of pages | 8 |
Journal | Research in Pharmaceutical Sciences |
Volume | 9 |
Issue number | 4 |
State | Published - Aug 2014 |
Externally published | Yes |
Keywords
- Appotosis
- Bax
- Disulfiram
- Human pancreatic cancerous cell line (PANC-1)
- p21
- RASSF1A
ASJC Scopus subject areas
- Pharmacology, Toxicology and Pharmaceutics(all)