期刊
DIGESTION
卷 91, 期 1, 页码 70-76出版社
KARGER
DOI: 10.1159/000369367
关键词
Activatable fluorescent probe; Colorectal tumor; Fluorescent imaging; gamma-Glutamyl hydroxymethyl rhodamine green; gamma-Glutamyl-transpeptidase
资金
- National Cancer Center Research and Development Fund [23-B-17]
- Grants-in-Aid for Scientific Research [25113707] Funding Source: KAKEN
Backgrounds/Aim: Colorectal laterally spreading tumors (LSTs) are sometimes difficult to visualize even with imageenhanced endoscopy. gamma-Glutamyl-transpeptidase (GGT) is a cell surface-associated enzyme that is overexpressed in various types of human cancers. Furthermore, GGT expression is higher in colorectal cancer cells than in normal colorectal mucosa. gamma-Glutamyl hydroxymethyl rhodamine green (gGlu-HMRG), an activatable fluorescent probe, is nonfluorescent under a neutral pH and normal cellular environment; however, it turns highly fluorescent upon reaction with GGT. We evaluated ex vivo fluorescent imaging of colorectal LSTs using this GGT-activatable fluorescent probe. Methods: Between March 2013 and March 2014, 30 endoscopically resected colorectal LSTs were prospectively included in this study. Each was analyzed by first taking a baseline image before spraying, then spraying with gGluHMRG onto the freshly resected specimen, and finally taking fluorescent images 15 min after spraying with a dedicated imaging machine. Results: Of the LSTs, 67% rapidly showed positive fluorescent activity. These activities were shown in adenoma (54%) and carcinoma in adenoma (76%), and in LST-granular type (80%) and LST-nongranular type (40%). Conclusion: Topically spraying gGlu-HMRG enabled rapid and selective fluorescent imaging of colorectal tumors owing to the upregulated GGT activity in cancer cells. (C) 2015 S. Karger AG, Basel
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