TY - JOUR
T1 - Assessing the anti-tumour properties of Iraqi propolis in vitro and in vivo
AU - Sulaiman, Ghassan M.
AU - Ad'hiah, Ali H.
AU - Al-Sammarrae, Khulood W.
AU - Bagnati, Renzo
AU - Frapolli, Roberta
AU - Bello, Ezia
AU - Uboldi, Sarah
AU - Romano, Michela
AU - Panini, Nicolò
AU - Scanziani, Eugenio
AU - Pezzolato, Marzia
AU - Erba, Eugenio
AU - D'Incalci, Maurizio
PY - 2012/5
Y1 - 2012/5
N2 - The study was designed to evaluate anti-tumour properties of Iraqi propolis collected from Mosul region (M) on HL-60 and HCT-116 cell lines and on HCT-116 in vivo. M induced an inhibitory effect against the proliferation of HL-60 and colony potential of HCT-116 cells. The apoptosis in HL-60 cells was associated with down-regulation of Bcl-2 and activation of Bax, while in HCT-116 cells, necrotic features were observed; size of cells was dramatically increased by swelling of cytoplasm and loss of membrane integrity, cell rupture and release of cellular contents. Analysis of BrdU/DNA cell cycle in both cell lines showed that M induced cell cycle perturbations in both BrdU positive and BrdU negative cells. The exposure of HL-60 to M caused γ-H2AX in a dose dependent manner and was associated with induction of apoptosis. The experiments in HCT-116 tumor-bearing mice showed that oral administration of propolis at doses that caused no detectable toxicity was associated with a decrease in mitotic cells and an increase in endoreduplications, increased p53 and decreased Ki-67 expression of cells in tumor sections. This study provides the rationale to investigate the potential beneficial effect of propolis in the diet of patients receiving anti-cancer therapies.
AB - The study was designed to evaluate anti-tumour properties of Iraqi propolis collected from Mosul region (M) on HL-60 and HCT-116 cell lines and on HCT-116 in vivo. M induced an inhibitory effect against the proliferation of HL-60 and colony potential of HCT-116 cells. The apoptosis in HL-60 cells was associated with down-regulation of Bcl-2 and activation of Bax, while in HCT-116 cells, necrotic features were observed; size of cells was dramatically increased by swelling of cytoplasm and loss of membrane integrity, cell rupture and release of cellular contents. Analysis of BrdU/DNA cell cycle in both cell lines showed that M induced cell cycle perturbations in both BrdU positive and BrdU negative cells. The exposure of HL-60 to M caused γ-H2AX in a dose dependent manner and was associated with induction of apoptosis. The experiments in HCT-116 tumor-bearing mice showed that oral administration of propolis at doses that caused no detectable toxicity was associated with a decrease in mitotic cells and an increase in endoreduplications, increased p53 and decreased Ki-67 expression of cells in tumor sections. This study provides the rationale to investigate the potential beneficial effect of propolis in the diet of patients receiving anti-cancer therapies.
KW - BrdU/DNA cell cycle
KW - Cytotoxicity
KW - Iraqi propolis
UR - http://www.scopus.com/inward/record.url?scp=84858257785&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84858257785&partnerID=8YFLogxK
U2 - 10.1016/j.fct.2012.01.022
DO - 10.1016/j.fct.2012.01.022
M3 - Article
C2 - 22306915
AN - SCOPUS:84858257785
SN - 0278-6915
VL - 50
SP - 1632
EP - 1641
JO - Food and Chemical Toxicology
JF - Food and Chemical Toxicology
IS - 5
ER -