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- PMID: 22350787
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Article: Ellagic acid, a phenolic compound, exerts anti-angiogenesis effects via VEGFR-2 signaling pathway in breast cancer
Title | Ellagic acid, a phenolic compound, exerts anti-angiogenesis effects via VEGFR-2 signaling pathway in breast cancer |
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Authors | |
Keywords | Anti-angiogenesis Breast cancer Ellagic acid Molecular docking VEGF/VEGFR2 |
Issue Date | 2012 |
Publisher | Springer New York LLC. The Journal's web site is located at http://springerlink.metapress.com/openurl.asp?genre=journal&issn=0167-6806 |
Citation | Breast Cancer Research And Treatment, 2012, v. 134 n. 3, p. 943-955 How to Cite? |
Abstract | Anti-angiogenesis targeting VEGFR-2 has been considered as an important strategy for cancer therapy. Ellagic acid is a naturally existing polyphenol widely found in fruits and vegetables. It was reported that ellagic acid interfered with some angiogenesis-dependent pathologies. Yet the mechanisms involved were not fully understood. Thus, we analyzed its anti-angiogenesis effects and mechanisms on human breast cancer utilizing in-vitro and in-vivo methodologies. The in-silico analysis was also carried out to further analyze the structure-based interaction between ellagic acid and VEGFR-2. We found that ellagic acid significantly inhibited a series of VEGF-induced angiogenesis processes including proliferation, migration, and tube formation of endothelial cells. Besides, it directly inhibited VEGFR-2 tyrosine kinase activity and its downstream signaling pathways including MAPK and PI3K/Akt in endothelial cells. Ellagic acid also obviously inhibited neo-vessel formation in chick chorioallantoic membrane and sprouts formation of chicken aorta. Breast cancer xenografts study also revealed that ellagic acid significantly inhibited MDA-MB-231 cancer growth and P-VEGFR2 expression. Molecular docking simulation indicated that ellagic acid could form hydrogen bonds and aromatic interactions within the ATP-binding region of the VEGFR-2 kinase unit. Taken together, ellagic acid could exert anti-angiogenesis effects via VEGFR-2 signaling pathway in breast cancer. © 2012 The Author(s). |
Persistent Identifier | http://hdl.handle.net/10722/145629 |
ISSN | 2023 Impact Factor: 3.0 2023 SCImago Journal Rankings: 1.267 |
ISI Accession Number ID |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Wang, N | en_HK |
dc.contributor.author | Wang, ZY | en_HK |
dc.contributor.author | Mo, SL | en_HK |
dc.contributor.author | Loo, TY | en_HK |
dc.contributor.author | Wang, DM | en_HK |
dc.contributor.author | Luo, HB | en_HK |
dc.contributor.author | Yang, DP | en_HK |
dc.contributor.author | Chen, YL | en_HK |
dc.contributor.author | Shen, JG | en_HK |
dc.contributor.author | Chen, JP | en_HK |
dc.date.accessioned | 2012-02-28T01:59:11Z | - |
dc.date.available | 2012-02-28T01:59:11Z | - |
dc.date.issued | 2012 | en_HK |
dc.identifier.citation | Breast Cancer Research And Treatment, 2012, v. 134 n. 3, p. 943-955 | en_HK |
dc.identifier.issn | 0167-6806 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/145629 | - |
dc.description.abstract | Anti-angiogenesis targeting VEGFR-2 has been considered as an important strategy for cancer therapy. Ellagic acid is a naturally existing polyphenol widely found in fruits and vegetables. It was reported that ellagic acid interfered with some angiogenesis-dependent pathologies. Yet the mechanisms involved were not fully understood. Thus, we analyzed its anti-angiogenesis effects and mechanisms on human breast cancer utilizing in-vitro and in-vivo methodologies. The in-silico analysis was also carried out to further analyze the structure-based interaction between ellagic acid and VEGFR-2. We found that ellagic acid significantly inhibited a series of VEGF-induced angiogenesis processes including proliferation, migration, and tube formation of endothelial cells. Besides, it directly inhibited VEGFR-2 tyrosine kinase activity and its downstream signaling pathways including MAPK and PI3K/Akt in endothelial cells. Ellagic acid also obviously inhibited neo-vessel formation in chick chorioallantoic membrane and sprouts formation of chicken aorta. Breast cancer xenografts study also revealed that ellagic acid significantly inhibited MDA-MB-231 cancer growth and P-VEGFR2 expression. Molecular docking simulation indicated that ellagic acid could form hydrogen bonds and aromatic interactions within the ATP-binding region of the VEGFR-2 kinase unit. Taken together, ellagic acid could exert anti-angiogenesis effects via VEGFR-2 signaling pathway in breast cancer. © 2012 The Author(s). | en_HK |
dc.language | eng | en_US |
dc.publisher | Springer New York LLC. The Journal's web site is located at http://springerlink.metapress.com/openurl.asp?genre=journal&issn=0167-6806 | en_HK |
dc.relation.ispartof | Breast Cancer Research and Treatment | en_HK |
dc.rights | The original publication is available at www.springerlink.com | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.subject | Anti-angiogenesis | en_HK |
dc.subject | Breast cancer | en_HK |
dc.subject | Ellagic acid | en_HK |
dc.subject | Molecular docking | en_HK |
dc.subject | VEGF/VEGFR2 | en_HK |
dc.title | Ellagic acid, a phenolic compound, exerts anti-angiogenesis effects via VEGFR-2 signaling pathway in breast cancer | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Shen, JG: shenjg@hku.hk | en_HK |
dc.identifier.email | Chen, JP: abchen@hku.hk | en_HK |
dc.identifier.authority | Shen, JG=rp00487 | en_HK |
dc.identifier.authority | Chen, JP=rp01316 | en_HK |
dc.description.nature | published_or_final_version | - |
dc.identifier.doi | 10.1007/s10549-012-1977-9 | en_HK |
dc.identifier.pmid | 22350787 | - |
dc.identifier.scopus | eid_2-s2.0-84868195812 | en_HK |
dc.identifier.hkuros | 198772 | en_US |
dc.identifier.spage | 1 | en_HK |
dc.identifier.epage | 13 | en_HK |
dc.identifier.isi | WOS:000307273300005 | - |
dc.publisher.place | United States | en_HK |
dc.identifier.scopusauthorid | Wang, N=16311384500 | en_HK |
dc.identifier.scopusauthorid | Wang, ZY=54989199500 | en_HK |
dc.identifier.scopusauthorid | Mo, SL=24921801300 | en_HK |
dc.identifier.scopusauthorid | Loo, TY=7006008583 | en_HK |
dc.identifier.scopusauthorid | Wang, DM=54985648900 | en_HK |
dc.identifier.scopusauthorid | Luo, HB=7401480124 | en_HK |
dc.identifier.scopusauthorid | Yang, DP=22959396400 | en_HK |
dc.identifier.scopusauthorid | Chen, YL=54990400400 | en_HK |
dc.identifier.scopusauthorid | Shen, JG=7404929947 | en_HK |
dc.identifier.scopusauthorid | Chen, JP=22733695400 | en_HK |
dc.identifier.citeulike | 10388800 | - |
dc.identifier.issnl | 0167-6806 | - |