Author/Authors :
Díaz-García, Alexis Research Department - Laboratories of Biopharmaceuticals and Chemistries Productions (LABIOFAM) - Havana, Cuba , Laura Ruiz-Fuentes, Jenny Microbiology Department - Tropical Medicine Institute “Pedro Kouri” - Havana, Cuba , Frión-Herrera, Yahima Department of Pharmaceutical Science - Padova University, Italy , Yglesias-Rivera, Arianna Research Department - Laboratories of Biopharmaceuticals and Chemistries Productions (LABIOFAM) - Havana, Cuba , Riquenez Garlobo, Yanelis Research Department - Laboratories of Biopharmaceuticals and Chemistries Productions (LABIOFAM) - Havana, Cuba , Rodríguez Sánchez, Hermis Microbiology Department - Tropical Medicine Institute “Pedro Kouri” - Havana, Cuba , Rodríguez Aurrecochea, Juan C Investigation Department - Laboratory of Experimental pathology - Oncology and Radiobiology National Institute - Havana, Cuba , X López Fuentes, Ledys Laboratory of Pathology - Tropical Medicine Institute “Pedro Kouri” - Havana, Cuba
Abstract :
Objective(s): In Cuba the endemic scorpion species Rhopalurus junceus has been used in traditional
medicine for cancer treatment and related diseases. However there is no scientific evidence about its
therapeutic potential for cancer treatment. The aim of the study was to determine the antitumor effect
of scorpion venom against a murine mammary adenocarcinoma F3II.
Materials and Methods: The cytotoxic activity was determined by MTT assay with venom concentrations
ranging from 0.1–1 mg/ml. Apoptosis was determined by RT-PCR and flow cytometry. Toxic effect in healthy
animals and tumor growth kinetics in F3II bearing-mice were evaluated by using scorpion venom doses
(0.2; 0.8; 3.2 mg/kg) after one and ten injections respectively by the intraperitoneal route.
Results: Scorpion venom induced a significant cytotoxic effect (P<0.05) in F3II cells in a concentrationdependent
manner. The cell death event involves the apoptotic pathway due to up-regulation of proapoptotic
genes (p53, bax), down-regulation of antiapoptotic gene (bcl-2), and 33% of Annexin V+/
PI- cells at early apoptosis and 10.21% of Annexin V+/PI+ cells at late apoptosis. Scorpion venom
induced significant inhibition of tumor progression (P<0.05) in F3II bearing-mice in a dose-dependent
manner. The antitumor effect was confirmed due to dose-dependent reduction of Ki-67 and CD31
proteins present in tumor tissue.
Conclusion: Evidence indicates that scorpion venom can be an attractive natural product for deep
investigation and developing a novel therapeutic agent for breast cancer treatment.
Keywords :
Antitumor , Apoptosis , Cytotoxicity , Murine mammary adenocarcinoma , Scorpion venom