Although several studies propose a chemopreventive effect of aspirin for colorectal cancer (CRC) development, the general use of aspirin cannot be recommended due to its adverse side effects. As the protective effect of aspirin has been associated with an increased expression of COX-2, molecular imaging of COX-2, for instance, during confocal endomicroscopy could enable the identification of patients who would possibly benefit from aspirin treatment. In this pilot trial, we used a COX-2-specific fluorescent probe for detection of colitis-associated and sporadic CRC in mice using confocal microscopy. Following the injection of the COX-2 probe into tumor-bearing APCmin mice or mice exposed to the AOM + DSS model of colitis-associated cancer, the tumor-specific upregulation of COX-2 could be validated with in vivo fluorescence imaging. Subsequent confocal imaging of tumor tissue showed an increased number of COX-2 expressing cells when compared to the normal mucosa of healthy controls. COX-2-expression was detectable with subcellular resolution in tumor cells and infiltrating stroma cells. These findings pose a proof of concept and suggest the use of CLE for the detection of COX-2 expression during colorectal cancer surveillance endoscopy. This could improve early detection and stratification of chemoprevention in patients with CRC.
Keyphrases
- poor prognosis
- low dose
- fluorescence imaging
- induced apoptosis
- fluorescent probe
- cardiovascular events
- high resolution
- living cells
- antiplatelet therapy
- high fat diet induced
- public health
- emergency department
- cell cycle arrest
- cardiovascular disease
- photodynamic therapy
- coronary artery disease
- type diabetes
- oxidative stress
- adipose tissue
- papillary thyroid
- combination therapy
- raman spectroscopy
- smoking cessation
- drug induced
- anti inflammatory drugs