Chiavacci Elena, Rizzo Milena, Pitto Letizia, Patella Francesca, Evangelista Monica, Mariani Laura, Rainaldi Giuseppe
Institute of Clinical Physiology, Area della Ricerca CNR, Via Moruzzi, 156124, Pisa, Italy.
Cytotechnology. 2015 Dec;67(6):969-75. doi: 10.1007/s10616-014-9735-y. Epub 2014 Jun 20.
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.
斑马鱼/肿瘤异种移植血管生成试验用于研究肿瘤血管生成,这是癌症进展中的关键步骤,也是抗肿瘤治疗的靶点。在此,我们评估了该试验是否能够鉴定具有抗血管生成潜力的微小RNA。为此,我们用四种对应用于人类脐静脉内皮细胞的抗血管生成和促血管生成刺激均有反应的微小RNA(miR-125a、miR-320、miR-487b、miR-492)转染DU-145前列腺癌细胞。转染后,将DU-145细胞注射到转基因Tg(Kdrl:eGFP)s843斑马鱼胚胎发育中的肠下血管附近,该胚胎在Kdrl启动子的控制下表达绿色荧光蛋白。在受精后72小时,我们观察到绿色荧光蛋白阳性的新血管侵入了用miR-125a、miR-320和miR-487b转染的DU-145移植瘤。反之,当使用用miR-492转染的DU-145细胞时,新血管形成和肿瘤细胞浸润受到抑制。这些结果表明,斑马鱼/肿瘤异种移植试验足以鉴定能够抑制血管生成性肿瘤细胞释放血管生成生长因子的微小RNA。