Cell-SELEX Aptamer for Highly Specific Radionuclide Molecular Imaging of Glioblastoma In Vivo

被引:58
|
作者
Wu, Xidong [1 ]
Liang, Huiyu [1 ]
Tan, Yan [1 ]
Yuan, Chao [2 ]
Li, Shuji [1 ]
Li, Xiaowen [1 ]
Li, Guiping [3 ]
Shi, Yusheng [4 ]
Zhang, Xingmei [1 ]
机构
[1] Southern Med Univ, Sch Basic Med Sci, Dept Neurobiol, Guangzhou, Guangdong, Peoples R China
[2] Southern Med Univ, Nanfang Hosp, Dept Neurol, Guangzhou, Guangdong, Peoples R China
[3] Southern Med Univ, Nanfang Hosp, Dept Nucl Med, Guangzhou, Guangdong, Peoples R China
[4] Southern Med Univ, Nanfang Hosp, Dept Radiat Oncol, Guangzhou, Guangdong, Peoples R China
来源
PLOS ONE | 2014年 / 9卷 / 03期
基金
美国国家科学基金会;
关键词
GROWTH-FACTOR RECEPTOR; EGFRVIII;
D O I
10.1371/journal.pone.0090752
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Glioblastoma (GBM) is the most frequent and aggressive primary adult brain tumor with poor prognosis. Epidermal growth factor receptor variant III (EGFRvIII) is the most common and highly oncogenic EGFR mutant in GBM. With the aim to generate specific molecular probes able to target EGFRvIII with high affinity, we selected four DNA aptamers (U2, U8, U19 and U31) specifically bound to U87-EGFRvIII cells that over expressed EGFRvIII with K-d values in the nanomole range by a cell-based systematic evolution of ligands by exponential enrichment (cell-SELEX) process. U87MG cells were introduced as control cells for counter selection. We further affirmed U2 and U8 identified EGFRvIII on the surface of target cells specifically. Then we radiolabeled U2 with 188Re to serve as a molecular imaging probe and observed 188Re -labeled U2 significantly targeted EGFRvIII over-expressing glioblastoma exnografts in mice. In conclusion, aptamers obtained from whole cell-SELEX strategy have great potential as molecular imaging probes that are probably beneficial to GBM diagnoses.
引用
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页数:8
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