期刊论文详细信息
Cancers
Effects of Ellagic Acid on Angiogenic Factors in Prostate Cancer Cells
Luca Vanella1  Claudia Di Giacomo1  Rosaria Acquaviva1  Ignazio Barbagallo1  Giovanni Li Volti1  Venera Cardile2  Nader G. Abraham3 
[1] Department of Drug Science, Section of Biochemistry, University of Catania, I-95125 Catania, Italy; E-Mails:;Department of Bio-Medical Sciences, Section of Physiology, University of Catania, I-95125, Catania, Italy; E-Mail:;Joan C. Edwards School of Medicine, Marshall University, Huntington, WV 25701, USA; E-Mail:
关键词: prostate cancer;    angiogenesis;    heme-oxygenase;    cytochrome P450;   
DOI  :  10.3390/cancers5020726
来源: mdpi
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【 摘 要 】

Background: Several natural antioxidants, including ellagic acid (EA), have been reported to have chemotherapeutic activity in vivo and in vitro settings. Cytochrome P450 (CYP) activity and synthesis of both epoxyeicosatrienoic acids (EETs) and 20-hydroxy-5,8,11,14-eicosatetraenoic acid (20-HETE), together with vascular endothelial growth factor (VEGF) and heme oxygenase system (HO) have emerged as important modulators of tumor growth and metastasis. Methods: The anti-angiogenic effects of EA were investigated in the human prostatic cancer cell line LnCap. HO-1, HO-2, CYP2J2 and soluble epoxyde hydrolase (sEH) expressions were evaluated by western blotting. Levels of VEGF and osteoprotegerin (OPG) were determined in the culture supernatant using an ELISA assay, while CYP mRNAs were determined by qRT-PCR. Results: EA treatment induced a significant decrease (p < 0.05) in HO-1, HO-2 and CYP2J2 expression, and in VEGF and OPG levels. Similarly CYP2J2, CYP4F2 and CYPA22 mRNAs were significantly (p < 0.05) down-regulated by EA treatment. The decrease in CYP2J2 mRNA was associated with an increase in sEH expression. Conclusions: Results reported in the present study highlighted the ability of EA to modulate a new pathway, in addition to anti-proliferative and pro-differentiation properties, via a mechanism that involves a decrease in eicosanoid synthesis and a down-regulation of the HO system in prostate cancer.

【 授权许可】

CC BY   
© 2013 by the authors; licensee MDPI, Basel, Switzerland.

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