The zebrafish/tumor xenograft angiogenesis assay as a tool for screening anti-angiogenic miRNAs

被引:23
作者
Chiavacci, Elena [1 ]
Rizzo, Milena [1 ]
Pitto, Letizia [1 ]
Patella, Francesca [1 ]
Evangelista, Monica [1 ]
Mariani, Laura [1 ]
Rainaldi, Giuseppe [1 ]
机构
[1] CNR, Inst Clin Physiol, Area Ric, I-156124 Pisa, Italy
关键词
microRNAs; Tumor angiogenesis; Zebrafish/tumor xenografts; Prostate tumor cells; GROWTH-FACTOR; KAPPA-B; HYPERGLYCEMIA; INSULIN; EMBRYO; CANCER; TUMORS; CELLS;
D O I
10.1007/s10616-014-9735-y
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The zebrafish/tumor xenograft angiogenesis assay is used to approach tumor angiogenesis, a pivotal step in cancer progression and target for anti-tumor therapies. Here, we evaluated whether the assay could allow the identification of microRNAs having an anti-angiogenic potential. For that, we transfected DU-145 prostate cancer cells with four microRNAs (miR-125a, miR-320, miR-487b, miR-492) responsive to both anti- and pro-angiogenic stimuli applied to human umbilical vein endothelial cells. After transfection, DU-145 cells were injected close to the developing subintestinal vessels of transgenic Tg(Kdrl:eGFP)s843 zebrafish embryos that express green fluorescent protein under the control of Kdrl promoter. At 72 h post-fertilization, we observed that green fluorescent protein-positive neo-vessels infiltrated the graft of DU-145 transfected with miR-125a, miR-320, and miR-487b. Vice versa, neo-vessel formation and tumor cell infiltration were inhibited when DU-145 cells transfected with miR-492 were used. These results indicated that the zebrafish/tumor xenograft assay was adequate to identify microRNAs able to suppress the release of angiogenic growth factors by angiogenic tumor cells.
引用
收藏
页码:969 / 975
页数:7
相关论文
共 28 条
[1]   Reactive oxygen generated by Nox1 triggers the angiogenic switch [J].
Arbiser, JL ;
Petros, J ;
Klafter, R ;
Govindajaran, B ;
McLaughlin, ER ;
Brown, LF ;
Cohen, C ;
Moses, M ;
Kilroy, S ;
Arnold, RS ;
Lambeth, JD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (02) :715-720
[2]   Angiogenesis in cancer and other diseases [J].
Carmeliet, P ;
Jain, RK .
NATURE, 2000, 407 (6801) :249-257
[3]   Angiogenesis in two human prostate cancer cell lines with differing metastatic potential when growing as solid tumors in nude mice [J].
Connolly, JM ;
Rose, DP .
JOURNAL OF UROLOGY, 1998, 160 (03) :932-936
[4]   Effects of simulated hyperglycemia, insulin, and glucagon on endothelial nitric oxide synthase expression [J].
Ding, YX ;
Vaziri, ND ;
Coulson, R ;
Kamanna, VS ;
Roh, DD .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2000, 279 (01) :E11-E17
[5]   Vascular endothelial growth factor as a target for anticancer therapy [J].
Ferrara, N .
ONCOLOGIST, 2004, 9 :2-10
[6]   Role of angiogenesis in tumor growth and metastasis [J].
Folkman, J .
SEMINARS IN ONCOLOGY, 2002, 29 (06) :15-18
[7]   High glucose induced nuclear factor kappa B mediated inhibition of endothelial cell migration [J].
Hamuro, M ;
Polan, J ;
Natarajan, M ;
Mohan, S .
ATHEROSCLEROSIS, 2002, 162 (02) :277-287
[8]   The hallmarks of cancer [J].
Hanahan, D ;
Weinberg, RA .
CELL, 2000, 100 (01) :57-70
[9]   Quantitative angiogenesis assays in vivo - A review [J].
Hasan J. ;
Shnyder S.D. ;
Bibby M. ;
Double J.A. ;
Bicknel R. ;
Jayson G.C. .
Angiogenesis, 2004, 7 (1) :1-16
[10]   High glucose-induced apoptosis in human vascular endothelial cells is mediated through NF-κB and c-Jun NH2-terminal kinase pathway and prevented by PI3K/Akt/eNOS pathway [J].
Ho, FM ;
Lin, WW ;
Chen, BC ;
Chao, CM ;
Yang, CR ;
Lin, LY ;
Lai, CC ;
Liu, SH ;
Liau, CS .
CELLULAR SIGNALLING, 2006, 18 (03) :391-399