Antitumoural and antiangiogenic activity of Portuguese propolis in in vitro and in vivo models

被引:35
作者
Silva-Carvalho, Ricardo [1 ,2 ]
Miranda-Goncalves, Vera [1 ,2 ]
Ferreira, Ana Margarida [3 ]
Cardoso, Susana M. [4 ]
Sobral, Abilio J. F. N. [5 ]
Almeida-Aguiar, Cristina [6 ]
Baltazar, Fatima [1 ,2 ]
机构
[1] Univ Minho, Sch Hlth Sci, Life & Hlth Sci Res Inst ICVS, P-4710057 Braga, Portugal
[2] ICVS 3Bs Govt Associate Lab, P-4710057 Braga, Portugal
[3] Univ Tras os Montes & Alto Douro, Chem Ctr Vila Real CQVR, Vila Real, Portugal
[4] Polytech Inst Coimbra Bencanta, Sch Agr, CERNAS, P-3045601 Coimbra, Portugal
[5] Univ Coimbra, Dept Chem, P-3004535 Coimbra, Portugal
[6] Univ Minho, Ctr Res & Technol Agroenvironm & Biol Sci, CITAB, P-4710057 Braga, Portugal
关键词
Portuguese propolis; Cancer; Antitumoural activity; Antiangiogenic activity; Cancer metabolism; ACID PHENETHYL ESTER; PROSTATE-CANCER CELLS; BRAZILIAN PROPOLIS; NATURAL-PRODUCTS; ANTIPROLIFERATIVE ACTIVITY; MATRIX-METALLOPROTEINASE; ANTIMICROBIAL ACTIVITY; INDUCED ANGIOGENESIS; CHEMICAL DIVERSITY; TUBE FORMATION;
D O I
10.1016/j.jff.2014.09.009
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Propolis, a natural product, has important biological properties, however, studies with Portuguese propolis are scarce. Thus, we aimed to characterize the chemical composition and the antitumoural and antiangiogenic activities of a sample from Pereiro (Portugal). The chemical profile of our propolis sample (P10.EE) is similar to the poplar propolis type. P10.EE decreased cell viability of different tumour cells, being less cytotoxic against non-tumoural cells. P10.EE decreased MDA-MB-231 and DU145 cell proliferation and migration, with cell cycle changes and increased cell death. The increased glucose consumption and lactate production in MDA-MB-231 cells is explained by an increased expression of different metabolism-related proteins. P10.EE induced a decrease in HBMEC cells total biomass and proliferation and decreased vessel sprouting in the chicken chorioallantoic membrane. Additionally, P10.EE potentiates paclitaxel effect in MDA-MB-231 and DU145 cells. Concluding, P10.EE can be a good candidate for cancer drug development since it affects different characteristics that dictate tumorigenesis. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:160 / 171
页数:12
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