Loading…

Efficacy and safety of aflibercept in in vitro and in vivo models of retinoblastoma

To evaluate the inhibitory effects of aflibercept on the growth and subretinal invasion of retinoblastoma. Xenotransplantation and orthotopic mouse models were created by injecting Y-79 cells subcutaneously and intravitreally, respectively. After induction of retinoblastoma, animals were intraperito...

Full description

Saved in:
Bibliographic Details
Published in:Journal of experimental & clinical cancer research 2016-11, Vol.35 (1), p.171-171, Article 171
Main Authors: Kim, Dong Yoon, Choi, Jeong A, Koh, Jae-Young, Yoon, Young Hee
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:To evaluate the inhibitory effects of aflibercept on the growth and subretinal invasion of retinoblastoma. Xenotransplantation and orthotopic mouse models were created by injecting Y-79 cells subcutaneously and intravitreally, respectively. After induction of retinoblastoma, animals were intraperitoneally injected with aflibercept (25 mg/kg body weight) or saline twice a week for 3 weeks. Tumor size was measured weekly and compared between the two groups. At 4 weeks, animals were sacrificed and an immunohistochemical examination was conducted to compare the microvascular density and degree of apoptosis between groups. In addition, the degree of choroidal invasion was also analyzed in the orthotopic xenotransplantation model. A co-culture system of Y-79 or WERI-Rb-1 cells and human umbilical vein endothelial cells (HUVECs) was used for in vitro experiments, and the anti-angiogenic effect of aflibercept was evaluated by analyzing cell numbers. In the Y-79 xenotransplantation model, aflibercept treatment significantly inhibited tumor growth at 4 weeks versus baseline compared with saline-injected mice (188.53 ± 118.53 mm vs. 747.87 ± 118.83 mm , respectively, P 
ISSN:1756-9966
0392-9078
1756-9966
DOI:10.1186/s13046-016-0451-7