Effect of sunitinib derivatives on glioblastoma single-cell migration and 3D cell cultures

被引:0
作者
Dabkeviciute, Girstaute [1 ,3 ]
Maccioni, Ellias [2 ]
Petrikaite, Vilma [1 ,3 ]
机构
[1] Vilnius Univ, Inst Biotechnol, Life Sci Ctr, Sauletekio Al 7, LT-10257 Vilnius, Lithuania
[2] Univ Cagliari, Dept Life & Environm Sci, Via Osped 72, I-09124 Cagliari, Italy
[3] Lithuanian Univ Hlth Sci, Inst Cardiol, Lab Drug Targets Histopathol, Sukileliu Pr 13, LT-50162 Kaunas, Lithuania
关键词
Sunitinib analogs; glioblastoma; tyrosine kinase inhibitors; spheroids; cell migration; THERAPY; HYPOXIA; GROWTH;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
This study aimed to evaluate the anticancer activity of 16 new sunitinib derivatives in brain cancer cells (2D model) and spheroids (3D model). The effect on cell viability was determined by the MTT assay. Single-cell migration assay was performed to examine the effect of selected compounds on individual cell migration. The activity of compounds in 3D cell cultures was examined by measuring the size change of spheroids formed using the Hanging drop method. The viability of brain cancer (U-87MG and A-172) cells was most reduced by compound EMAC4001. EMAC4001 showed the strongest effect on U-87MG cell migration, and EMAC4007 was the most active in the A-172 cell line. Only sunitinib had a statistically significant impact on spheroid growth at 100 nM and 500 nM concentrations in the U87-MG cell line and EMAC4007 had a statistically significant impact on A-172 spheroid growth at 100 nM and 500 nM concentrations, similarly to sunitinib.
引用
收藏
页码:1377 / 1386
页数:10
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