Anti-angiogenic potential of an ethanol extract of Annona atemoya seeds in vitro and in vivo

被引:18
|
作者
Yi, Jin-Mu [1 ,3 ]
Park, Jong-Shik [1 ]
Lee, Jun [1 ]
Hong, Jin Tae [3 ]
Bang, Ok-Sun [1 ]
Kim, No Soo [1 ,2 ]
机构
[1] Korea Inst Oriental Med, KM Based Herbal Drug Dev Grp, Taejon 305811, South Korea
[2] Korea Univ Sci & Technol, Dept Korean Med Life Sci & Technol, Taejon, South Korea
[3] Chungbuk Natl Univ, Coll Pharm, Cheongju, South Korea
关键词
Annona atemoya; Angiogenesis; Anticancer; HIF; VEGF; HYPOXIA-INDUCIBLE FACTOR; ENDOTHELIAL GROWTH-FACTOR; GENE-EXPRESSION; CANCER CELLS; ACETOGENIN; MECHANISMS; SQUAMOSA; YC-1; CYCLOOXYGENASE-2; HIF-1-ALPHA;
D O I
10.1186/1472-6882-14-353
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Background: Angiogenesis, which is initiated by certain tumor micro-environmental conditions and diverse protein factors, plays a pivotal role during tumor development and metastasis. Therefore, many efforts have been made to develop effective anti-angiogenic agents as anticancer therapeutics. In the current study, we investigated the anti-angiogenic potential of an ethanol extract of Annona atemoya seeds (EEAA) in vitro and in vivo. Methods: The anti-angiogenic potential of EEAA was evaluated using various in vitro/in vivo models, including cell proliferation, migration, and tube formation by human umbilical vascular endothelial cells (HUVECs); a Matrigel plug assay; and tumor-induced angiogenesis. The expression of hypoxia-inducible factors (HIFs) and vascular endothelial growth factor (VEGF) was investigated using reverse transcription-polymerase chain reaction, immunoassays, and western blotting. Results: EEAA was able to significantly inhibit the angiogenic properties of HUVECs in vitro as well as angiogenic factor-induced blood vessel formation in vivo. EEAA down-regulated the expression of VEGF and HIF-1alpha/2alpha at the mRNA and protein levels, respectively, in cancer cells under hypoxic conditions. Conclusions: EEAA shows a strong anti-angiogenic potential in both in vitro and in vivo systems, and we suggest that EEAA may be a valuable herbal source for anticancer drug development.
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收藏
页数:10
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