Grimm Jan, Kirsch David G, Windsor Stephen D, Kim Carla F Bender, Santiago Philip M, Ntziachristos Vasilis, Jacks Tyler, Weissleder Ralph
Center for Molecular Imaging Research and Department of Radiation Oncology, Massachusetts General Hospital and Harvard Medical School, Charlestown, MA 02129, USA.
Proc Natl Acad Sci U S A. 2005 Oct 4;102(40):14404-9. doi: 10.1073/pnas.0503920102. Epub 2005 Sep 23.
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.
通过基因表达谱分析,我们在人肺腺癌小鼠模型中鉴定出组织蛋白酶半胱氨酸蛋白酶为高度上调基因。通过免疫组织化学和蛋白质印迹法证实了这些肺肿瘤中组织蛋白酶的过表达。因此,选择了一种由组织蛋白酶激活的光学探针来在体内检测直径小至1毫米且空间分离的小鼠肺肿瘤。我们生成了荧光信号的3D图谱,并将其与解剖学计算机断层扫描图像融合,以显示荧光信号与肿瘤负荷之间的密切相关性。通过对同一只小鼠进行连续成像,利用光学成像跟踪肿瘤进展。这项研究证明了利用肿瘤表达的内源性蛋白酶对原发性肺肿瘤进行分子成像的能力。它还强调了利用基因表达谱分析来识别肺癌成像分子靶点的可行性。