Author/Authors :
Hamedi Azadeh نويسنده Department of Pharmaceutical Biotechnology, School of Pharmacy, Shiraz University of Medical Sciences, Shiraz, IR Iran Hamedi Azadeh , Jaafari-Ashkavandi Zohreh نويسنده Dept. of Oral and Maxillofacial Pathology, School of Dentistry, Shiraz University of Medical Sciences, Shiraz, Iran. , Ebrahimpour Azin نويسنده , Assar Sepideh نويسنده Department of Oral and Maxillofacial Pathology, Shiraz
Dental School, Shiraz University of Medical Sciences, Shiraz, IR
Iran
Abstract :
Background Cytotoxic effects of Frankincense resin have been shown
on some cancer cell lines. Due to its low side effects, this study was
designed to evaluate the anticancer properties of water soluble elements
of Frankincense oleo-gum-resin on human oral squamous cell carcinoma
cell line. Methods Oleo-gum-resin was macerated in ethanol. After
filtration, the water soluble fraction of dried residue was extracted.
KB cells were treated with 0, 62.5, 125, 250 and 500 μg/mL
concentrations of obtained Frankincense aqueous fractions and with
Doxorubicin as positive control. Frankincense induced cell cytotoxicity;
apoptosis and proliferation were investigated using WST assay, Annexin
V-FITC/PI, and Ki-67 staining, respectively. Data were analyzed using
Kruskal-Wallis test by SPSS 17 software. Results
IC50 of 137.21 μg/mL was obtained from
Frankincense aqueous fraction after 48 hours. The percentage of
apoptotic cells was elevated in a time- and dose-dependent manner. There
was no statistical difference in the Ki-67 expression of KB cells, using
different concentration of Frankincense aqueous fraction after 24 and 48
hours (P = 0.083). Doxorubicin inhibited cells growth essentially
through apoptosis. Conclusions Frankincense aqueous fractions seem to
suppress KB cell growth through the induction of apoptosis and necrosis
rather than the inhibition of proliferation and hence might be a
potential anticancer agent. Structural analysis and purification of
potent components are suggested for determining more definitive results.