Cultivated Orostachys japonicus extract inhibits VEGF-induced angiogenesis via regulation of VEGFR2 signaling pathway in vitro and in vivo

被引:10
作者
Cho, Hyun-Dong [1 ]
Lee, Kwan-Woo [2 ]
Won, Yeong-Seon [2 ]
Kim, Jeong-Ho [3 ]
Seo, Kwon-Il [2 ]
机构
[1] Dong A Univ, Ind Acad Cooperat, Busan 49315, South Korea
[2] Dong A Univ, Dept Biotechnol, 37,Nakdong Daero 550 St, Busan 49315, South Korea
[3] Kyungpook Natl Univ, Dept Food Sci & Biotechnol, Daegu 41566, South Korea
基金
新加坡国家研究基金会;
关键词
Angiogenesis; Cultivated Orostachys japonicus; Vascular endothelial growth factor receptor 2; ENDOTHELIAL GROWTH-FACTOR; CELL-CYCLE ARREST; TISSUE INHIBITOR; MECHANISMS; CANCER; METASTASIS; INVASION; SUPPRESSION; FLAVONOIDS; MIGRATION;
D O I
10.1016/j.jep.2020.112664
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Ethnopharmacological relevance: Orostachys japonicus A. Berger (O. japonicus), so-called Wa-song in Korea, a traditional food and medicine that grows on mountain rocks and roof files. Wa-song containing various phenolic compounds have been reported as a medicinal plant for prevention of fibrosis, cancer, inflammation, and oxidative damage. Aim of the study: The present study was designed to examine the anti-angiogenic effects of cultivated Orostachys japonicus 70% ethanol extract (CE) in vascular endothelial growth factor (VEGF)-stimulated human umbilical vein endothelial cells (HUVECs). Materials and methods: CE was prepared with 70% ethanol. HUVECs, rat aortic rings, and matrigel plug in mice were treated with CE (10-20 mu g/mL) and VEGF (20-50 ng/mL), and the anti-angiogenic activities of CE were analyzed by SRB, wound healing, trans-well invasion, capillary-like tubule formation, rat aortas, Western blot, and matrigel plug assay. Phenolic compounds in CE were analyzed using a high-performance liquid chromatography (HPLC)-PDA system. Results: Treatment of CE (10-20 mu g/mL) markedly suppressed proliferation of HUVECs in the presence (from 136.5% to 112.2%) or absence of VEGF (from 100.0% to 92.1%). The proliferation inhibitory effect of CE was caused by G0/G1 cell cycle arrest, and the decrease of CDK-2, CDK-4, Cyclin D1 and Cyclin E1. Furthermore, CE treatment showed significant angiogenesis inhibitory effects on motility, invasion and micro-vessel formation of HUVECs, rat aortic rings and subcutaneous matrigels under VEGF-stimulation condition. In HUVECs, CE-induced anti-angiogenic effect was regulated by inhibition of the PI3K/AKT/mTOR, MAPK/p38, MAPK/ERK, FAK-Src, and VEGF-VEGFR2 signaling pathways. Conclusion: This study demonstrated that CE might be used as a potential natural substance, multi-targeted angiogenesis inhibitor, functional food material.
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页数:11
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共 62 条
[31]  
Lee Sanghyun, 2004, Natural Product Sciences, V10, P306
[32]   Bioconverted Orostachys japonicas Extracts Suppress Angiogenic Activity of Ms-1 Endothelial Cells [J].
Lee, Seul Gi ;
Kim, Jin Soo ;
Lee, Han-Saem ;
Lim, Yu-Mi ;
So, Jai-Hyun ;
Hahn, Dongyup ;
Ha, Yu Shin ;
Nam, Ju-Ock .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2017, 18 (12)
[33]  
Mazzanti R, 1997, HEPATOLOGY, V25, P229, DOI 10.1053/jhep.1997.v25.pm0008985296
[34]   Angiogenesis in chronic inflammatory liver disease [J].
Medina, J ;
Arroyo, AG ;
Sánchez-Madrid, F ;
Moreno-Otero, R .
HEPATOLOGY, 2004, 39 (05) :1185-1195
[35]   A cell penetrating peptide derived from azurin inhibits angiogenesis and tumor growth by inhibiting phosphorylation of VEGFR-2, FAK and Akt [J].
Mehta, Rajeshwari R. ;
Yamada, Tohru ;
Taylor, Brad N. ;
Christov, Konstantin ;
King, Marissa L. ;
Majumdar, Dibyen ;
Lekmine, Fatima ;
Tiruppathi, Chinnaswamy ;
Shilkaitis, Anne ;
Bratescu, Laura ;
Green, Albert ;
Beattie, Craig W. ;
Das Gupta, Tapas K. .
ANGIOGENESIS, 2011, 14 (03) :355-369
[36]   Critical Role of Aberrant Angiogenesis in the Development of Tumor Hypoxia and Associated Radioresistance [J].
Multhoff, Gabriele ;
Radons, Juergen ;
Vaupel, Peter .
CANCERS, 2014, 6 (02) :813-828
[37]   Knockdown of VEGFR2 inhibits proliferation and induces apoptosis in hemangioma-derived endothelial cells [J].
Ou, J. M. ;
Yu, Z. Y. ;
Qiu, M. K. ;
Dai, Y. X. ;
Dong, Q. ;
Shen, J. ;
Dong, P. ;
Wang, X. F. ;
Liu, Y. B. ;
Quan, Z. W. ;
Fei, Z. W. .
EUROPEAN JOURNAL OF HISTOCHEMISTRY, 2014, 58 (01) :65-72
[38]  
Pratheeshkumar P, 2012, PLOS ONE, V7, DOI [10.1371/journal.pone.0052279, 10.1371/journal.pone.0047516]
[39]   Inhibition of TIMP1 enhances angiogenesis in vivo and cell migration in vitro [J].
Reed, MJ ;
Koike, T ;
Sadoun, E ;
Sage, EH ;
Puolakkainen, P .
MICROVASCULAR RESEARCH, 2003, 65 (01) :9-17
[40]   Antiangiogenic compounds: well-established drugs versus emerging natural molecules [J].
Ribeiro, Andreia ;
Abreu, Rui M. V. ;
Dias, Madalena M. ;
Barreiro, Maria Filomena ;
Ferreira, Isabel C. F. R. .
CANCER LETTERS, 2018, 415 :86-105