Endoscopic detection of murine colonic dysplasia using a novel fluorescence-labeled peptide

被引:0
|
作者
Miller, Sharon J. [1 ]
Joshi, Bishnu P. [1 ]
Gaustad, Adam [2 ]
Fearon, Eric R. [1 ,3 ,4 ,5 ]
Wang, Thomas D. [1 ,2 ,5 ]
机构
[1] Univ Michigan, Dept Internal Med, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Biomed Engn, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Dept Human Genet, Ann Arbor, MI 48109 USA
[4] Univ Michigan, Dept Pathol, Ann Arbor, MI 48109 USA
[5] Univ Michigan, Canc Ctr, Ann Arbor, MI 48109 USA
来源
ENDOSCOPIC MICROSCOPY VI | 2011年 / 7893卷
基金
美国国家卫生研究院;
关键词
Wide-field endoscopy; phage display; fluorescent imaging; peptide; colonic dysplasia; COLORECTAL-CANCER; FLAT ADENOMAS; COLONOSCOPY; CARCINOMA; PHAGE; MICE;
D O I
10.1117/12.873530
中图分类号
TH742 [显微镜];
学科分类号
摘要
Current endoscopic screening does not detect all pre-malignant (dysplastic) colorectal mucosa, thus requiring the development of more sensitive, targeted techniques to improve detection. The presented work utilizes phage display to identify a novel peptide binder to colorectal dysplasia in a CPC; Apc mouse model. A wide-field, small animal endoscope capable of fluorescence excitation (450-475 nm) identified polyps via white light and also collected fluorescence images (510 nm barrier filter) of peptide binding. The peptide bound similar to 2-fold greater to the colonic adenomas when compared to the control peptide. We have imaged fluorescence-labeled peptide binding in vivo that is specific towards distal colonic adenomas.
引用
收藏
页数:8
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