Assessment of bevacizumab resistance increased by expression of BCAT1 in IDH1 wild-type glioblastoma: application of DSC perfusion MR imaging

被引:14
|
作者
Cho, Hye Rim [1 ,2 ]
Hong, Bora [1 ,2 ]
Kim, Hyeonjin [1 ]
Park, Chul-Kee [3 ]
Park, Sung-Hye [4 ]
Park, Sunghyouk [5 ]
Choi, Seung Hong [1 ,2 ]
机构
[1] Seoul Natl Univ Hosp, Dept Radiol, Seoul, South Korea
[2] Inst for Basic Sci Korea, Ctr Nanoparticle Res, Seoul, South Korea
[3] Seoul Natl Univ Hosp, Dept Neurosurg, Seoul, South Korea
[4] Seoul Natl Univ Hosp, Dept Pathol, Seoul, South Korea
[5] Seoul Natl Univ, Nat Prod Res Inst, Coll Pharm, Seoul, South Korea
关键词
BCAT1; dynamic susceptibility contrast (DSC); bevacizumab; glioblastoma; BLOOD-VOLUME MAPS; CELL-PROLIFERATION; ANTIANGIOGENIC THERAPY; GLIOMAS; PROGRESSION; SURVIVAL; GRADE; DIFFUSION; TIME; QUANTITATION;
D O I
10.18632/oncotarget.11901
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BCAT1 (branched-chain amino acid trasaminase1) expression is necessary for the progression of IDH1 wild-type (WT) glioblastoma multiforme (GBM), which is known to be associated with aggressive tumors. The purpose of our study is to investigate the bevacizumab resistance increased by the expression of BCAT1 in IDH1 WT GBM in a rat model, which was evaluated using DSC perfusion MRI. BCAT1 sh#1 inhibits cell proliferation and limits cell migration potential in vitro. In vivo MRI showed that the increase in both tumor volume and nCBV after bevacizumab treatment in IDH1 WT tumors was significantly higher compared with BCAT1 sh#1 tumors. In a histological analysis, more micro-vessel reformation by bevacizumab resistance was observed in IDH1 WT tumors than BCAT1 sh#1 tumors. These findings indicate that BCAT1 expression in IDH1 WT GBM increases resistance to bevacizumab treatment, which could be assessed by DSC perfusion MRI, and that nCBV can be a surrogate imaging biomarker for the prediction of antiangiogenic treatment in GBM.
引用
收藏
页码:69606 / 69615
页数:10
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