Use of gene expression profiling to direct in vivo molecular imaging of lung cancer

被引:110
作者
Grimm, J
Kirsch, DG
Windsor, SD
Kim, CFB
Santiago, PM
Ntziachristos, V
Jacks, T
Weissleder, R [1 ]
机构
[1] Massachusetts Gen Hosp, Ctr Mol Imaging Res, Charlestown, MA 02129 USA
[2] Massachusetts Gen Hosp, Dept Radiat Oncol, Charlestown, MA 02129 USA
[3] Harvard Univ, Sch Med, Charlestown, MA 02129 USA
[4] MIT, Dept Biol, Cambridge, MA 02139 USA
[5] MIT, Canc Res Ctr, Cambridge, MA 02139 USA
[6] MIT, Howard Hughes Med Inst, Cambridge, MA 02139 USA
关键词
D O I
10.1073/pnas.0503920102
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
Using gene expression profiling, we identified cathepsin cysteine proteases as highly up-regulated genes in a mouse model of human lung adenocarcinoma. Overexpression of cathepsin proteases in these lung tumors was confirmed by immunohistochemistry and Western blotting. Therefore, an optical probe activated by cathepsin proteases was selected to detect murine lung tumors in vivo as small as 1 mm in diameter and spatially separated. We generated 3D maps of the fluorescence signal and fused them with anatomical computed tomography images to show a close correlation between fluorescence signal and tumor burden. By serially imaging the same mouse, optical imaging was used to follow tumor progression. This study demonstrates the capability for molecular imaging of a primary lung tumor by using endogenous proteases expressed by a tumor. It also highlights the feasibility of using gene expression profiling to identify molecular targets for imaging lung cancer.
引用
收藏
页码:14404 / 14409
页数:6
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