Near-Infrared Fluorescence Imaging Using a Protease-Specific Probe for the Detection of Colon Tumors

作者:Yoon Soon Man; Myung Seung Jae*; Ye Byong Duk; Kim In Wha; Lee Nam Gon; Ryu Yeon Mi; Park Kyeongsoon; Kim Kwangmeyung; Kwon Ick Chan; Park Young Soo; Park Chan Sik; Moon Dae Hyuk; Kim Do Hoon; Do Mi Young; Byeon Jeong Sik; Yang Suk Kyun; Kim Jin Ho
来源:Gut and Liver, 2010, 4(4): 488-497.
DOI:10.5009/gnl.2010.4.4.488

摘要

Background/Aims: Early tumor detection is crucial for the prevention of colon cancer. Near-infrared fluorescence (NIRF) imaging using a target-activatable probe may permit earlier disease detection. Matrix metalloproteinases (MMPs) participate in tumorigenesis and tumor growth. The aim of this study was to determine whether NIRF imaging using an MMP-activatable probe can detect colon tumors at early stages. Methods: We utilized two murine colon cancer models: a sporadic colon cancer model induced by azoxy-methane (AOM), and a colitis-associated cancer model induced by a combination of AOM and dextran sodium sulfate (DSS). Colonic lesions were analyzed by histologic examination, Western blotting, immunohistochemical staining, and NIRF imaging using an MMP-activatable probe. Results: Multiple variable-sized tumors developed in both models and progressed from adenomas to adenocarcinomas over time. At the early stage of the AOM/DSS model, diffuse inflammation was observed within the tumors. MMP expression increased progressively through normal, inflammation, adenoma, and adenocarcionoma stages. NIRF signal intensities were strongly correlated with each tumor stage from adenoma to adenocarcinoma. NIRF imaging also distinguished tumors from inflamed mucosa. Conclusions: NIRF imaging using a protease-activatable probe may be a useful tool for early tumor detection. This approach could translate to improve the endoscopic detection of colon tumors, especially in patients with inflammatory bowel disease. (Gut Liver 2010;4:488-497)

  • 出版日期2010-12