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10.1590/1678-9199-jvatitd-2019-0009
 

Research article - Vol. 25, 2019

 

Cytotoxic effects of Pseudocerastes persicus venom and its HPLC fractions on lung cancer cells

 

Benyamin Shahbazi1, Zahra Salehi Najafabadi2, Hamidreza Goudarzi2, Mahnaz Sajadi3, Fatemeh Tahoori2, Masoumeh Bagheri2

 

1 Payame Noor University of Tehran Shargh, Tehran, Iran.

2 Razi Vaccine and Serum Research Institute, Agricultural Research, Education and Extension Organization, Karaj, Iran.

3 Tofigh Daru Research and Engineering Company, Tehran, Iran.

 

ABSTRACT

Background:

Several studies have pointed out that certain snake venoms contain compounds presenting cytotoxic activities that selectively interfere with cancer cell metabolism. In this study, Pseudocerastes persicus venom and its fractions were investigated for their anticancer potential on lung cancer cells.

Methods:

Lung cancer cells (A549) and normal fibroblast cells (Hu02) were treated with the P. persicus venom and its HPLC fractions and the cell cytotoxic effects were analyzed using MTT and lactate dehydrogenase release assays. Apoptosis was determined in venom-treated cell cultures using caspase-3 and caspase-9 assay kits.

Results:

The treatment of cells with HPLC fraction 21 (25-35 kDa) of P. persicus venom resulted in high LDH release in normal fibroblast cells and high caspase-3 and caspase-9 activities in lung cancer cells. These results indicate that fraction 21 induces apoptosis in cancer cells, whereas necrosis is predominantly caused by cell death in the normal cells. Fraction 21 at the final concentration of 10 μg/mL killed approximately 60% of lung cancer cells, while in normal fibroblast cells very low cell cytotoxic effect was observed.

Conclusion:

HPLC fraction 21 at low concentrations displayed promising anticancer properties with apoptosis induction in the lung cancer cells. This fraction may, therefore, be considered a promising candidate for further studies.

 

Keywords Pseudocerastes persicus venom; Persian horned viper; HPLC fractions; Cytotoxicity; Apoptosis

 

Received: February 27, 2019.

Accepted: August 06, 2019.

 

Correspondence: zahra.salehi@live.com

 

Authors' contributions

ZSN and HG analyzed and interpreted the biochemical data regarding the cytotoxicity effects of the venom. ZSN and FT prepared HPLC fractions of venom. BS and MS performed the in vitro cytotoxicity assays. All authors read and approved the final manuscript.