Document Type : Research Articles
Department of Biology, Science and Research Branch, Islamic Azad University, Tehran, Iran.
The Lister Laboratory of Microbiology, Tehran, Iran.
Department of Microbiology and Virology, Faculty of Medicine, Zanjan University of Medical Sciences, Zanjan, Iran.
Department of Biotechnology, School of Advanced Technologies in Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Department of Cellular and Molecular Biology, Ahar Branch, Islamic Azad University, Tabriz, Iran.
Young Researchers and Elite Club, East Tehran Branch, Islamic Azad University, Tehran, Iran.
Introduction: Linum album is a medicinal plant endemic in Iran that is very important pharmaceutically. The present
study concerns the effect of different extracts of L. album on ZNF703 gene expression and apoptosis in human gastric
carcinoma AGS cells. Method and material: Hydro alchoholic L. album extracts from various plant sources were
produced by Maceration. AGS cells were treated with different concentrations (200, 400, 600, 800 and 1000 μg/ml)
and the cytotoxicity potency was assessed after 24 h by MTT assay. Then, quantitative real time PCR was conducted
for ZNF703 gene expression in AGS cells. Also, cell apoptosis/necrosis was assessed with the aid of Annexin V/PI
staining and quantification by flow cytometry. Results: L. album extracts exerted dose-dependent toxicity in the AGS
cell line. The mRNA levels of ZNF703 gene expression were significantly decreased with rhizome, fruit at fruiting,
leaf and stem at anthesis (P<0.001), and leaf and stem at fruiting extracts as compared to the controls (P<0.01). Also,
the number of apoptotic cells was increased from 2.70% (statistically significant; p<0.05) in untreated AGS cells to 44%,
following treatment with the leaf and stem at anthesis example. Discussion: Our findings revealed that the L. album
extracts can induce apoptosis and might modulate cytotoxicity by down regulating ZNF703 gene expression in AGS
cells. Therefore, this extract could be a good candidate for inhibiting cancer cell growth, especially that of gastric
cancer. In addition, ZNF703 may have potential as a therapeutic target.