Marine Bromophenol Bis(2,3,6-Tribromo-4,5-Dihydroxybenzyl)ether Inhibits Angiogenesis in Human Umbilical Vein Endothelial Cells and Reduces Vasculogenic Mimicry in Human Lung Cancer A549 Cells

被引:11
作者
Dong, Songtao [1 ,2 ]
Chen, Zhongyuan [1 ]
Wang, Li [1 ]
Liu, Yankai [1 ]
Stagos, Dimitrios [3 ]
Lin, Xiukun [4 ]
Liu, Ming [1 ,2 ]
机构
[1] Ocean Univ China, Sch Med & Pharm, Key Lab Marine Drugs, Minist Educ China, 5 Yushan Rd, Qingdao 266003, Shandong, Peoples R China
[2] Lab Marine Drugs & Bioprod, Qingdao Natl Lab Marine Sci & Technol, Qingdao 266237, Shandong, Peoples R China
[3] Univ Thessaly, Sch Hlth Sci, Dept Biochem & Biotechnol, Larisa 41500, Greece
[4] Southwest Med Univ, Sch Pharm, Dept Pharmacol, 319 Zhongshan Rd, Jiangyang 646000, Luzhou, Peoples R China
关键词
anti-angiogenesis; bromophenols; tube formation; vasculogenic mimicry; RED ALGA; SYMPHYOCLADIA-LATIUSCULA; IN-VITRO; TUMOR; VEGF; ETHER; METASTASIS; MECHANISMS; INVASION; PHENOLS;
D O I
10.3390/md19110641
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Angiogenesis, including the growth of new capillary blood vessels from existing ones and the malignant tumors cells formed vasculogenic mimicry, is quite important for the tumor metastasis. Anti-angiogenesis is one of the significant therapies in tumor treatment, while the clinical angiogenesis inhibitors usually exhibit endothelial cells dysfunction and drug resistance. Bis(2,3,6-tribromo-4,5-dihydroxybenzyl)ether (BTDE), a marine algae-derived bromophenol compound, has shown various biological activities, however, its anti-angiogenesis function remains unknown. The present study illustrated that BTDE had anti-angiogenesis effect in vitro through inhibiting human umbilical vein endothelial cells migration, invasion, tube formation, and the activity of matrix metalloproteinases 9 (MMP9), and in vivo BTDE also blocked intersegmental vessel formation in zebrafish embryos. Moreover, BTDE inhibited the migration, invasion, and vasculogenic mimicry formation of lung cancer cell A549. All these results indicated that BTDE could be used as a potential candidate in anti-angiogenesis for the treatment of cancer.
引用
收藏
页数:14
相关论文
共 53 条
[1]   INHIBITION OF INVASION, GELATINASE ACTIVITY, TUMOR TAKE AND METASTASIS OF MALIGNANT-CELLS BY N-ACETYLCYSTEINE [J].
ALBINI, A ;
DAGOSTINI, F ;
GIUNCIUGLIO, D ;
PAGLIERI, I ;
BALANSKY, R ;
DEFLORA, S .
INTERNATIONAL JOURNAL OF CANCER, 1995, 61 (01) :121-129
[2]   Inhibition of protein phosphatase 2A sensitizes pancreatic cancer to chemotherapy by increasing drug perfusion via HIF-1α-VEGF mediated angiogenesis [J].
Bai, Xueli ;
Zhi, Xiao ;
Zhang, Qi ;
Liang, Feng ;
Chen, Wei ;
Liang, Chao ;
Hu, Qida ;
Sun, Xu ;
Zhuang, Zhengping ;
Liang, Tingbo .
CANCER LETTERS, 2014, 355 (02) :281-287
[3]  
Cai T, 1999, LAB INVEST, V79, P1151
[4]   Tumor cell-mediated neovascularization and lymphangiogenesis contrive tumor progression and cancer metastasis [J].
Cao, Zhifei ;
Shang, Bingxue ;
Zhang, Gaochuan ;
Miele, Lucio ;
Sarkar, Fazlul H. ;
Wang, Zhiwei ;
Zhou, Quansheng .
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER, 2013, 1836 (02) :273-286
[5]   VEGF as a key mediator of angiogenesis in cancer [J].
Carmeliet, P .
ONCOLOGY, 2005, 69 :4-10
[6]   Angiogenesis in cancer and other diseases [J].
Carmeliet, P ;
Jain, RK .
NATURE, 2000, 407 (6801) :249-257
[7]   SELECTIVE TARGETING OF THE TUMOUR VASCULATURE [J].
Chan, Lie S. ;
Daruwalla, Jurstine ;
Christophi, Christopher .
ANZ JOURNAL OF SURGERY, 2008, 78 (11) :955-967
[8]  
Childs S, 2002, DEVELOPMENT, V129, P973
[9]   Cancer therapy - Matrix metalloproteinase inhibitors and cancer: Trials and tribulations [J].
Coussens, LM ;
Fingleton, B ;
Matrisian, LM .
SCIENCE, 2002, 295 (5564) :2387-2392
[10]   Rapid analysis of angiogenesis drugs in a live fluorescent zebrafish assay [J].
Cross, LM ;
Cook, MA ;
Lin, S ;
Chen, JN ;
Rubinstein, AL .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2003, 23 (05) :911-912