N6-isopentenyladenosine a new potential anti-angiogenic compound that targets human microvascular endothelial cells <i>in vitro</i>
作者:Sara Castiglioni、Valentina Romeo、Silvana Casati、Roberta Ottria、Cristiana Perrotta、Pierangela Ciuffreda、Jeanette A. M. Maier
DOI:10.1080/15257770.2018.1503673
日期:2018.10.3
significant reduction of cell viability, upregulated p21 and promoted caspase-3 cleavage in a dose dependent manner leading to apoptotic cell death as detected by FACS analysis. To understand structure-function relationship of N6-isopentenyladenosine, we investigated the effect of some N6-isopentenyladenosine analogs. Our results suggest that N6-isopentenyladenosine and some of its derivatives are potentially
摘要 N6-异戊烯基腺苷是一种对正常细胞和肿瘤细胞具有抗增殖和促凋亡作用的非典型核苷。考虑到血管生成在各种疾病中的作用,我们研究了 N6-异戊烯基腺苷对人微血管内皮细胞(血管生成的主角)的细胞毒作用。我们的结果表明,N6-异戊烯基腺苷以剂量依赖性方式诱导细胞活力的显着降低,上调 p21 并促进 caspase-3 切割,导致 FACS 分析检测到的细胞凋亡。为了了解 N6-异戊烯基腺苷的结构-功能关系,我们研究了一些 N6-异戊烯基腺苷类似物的作用。