Hensley Harvey, Cooper Harry S, Chang Wen-Chi L, Clapper Margie L
Biological Imaging Facility, Fox Chase Cancer Center, 333 Cottman Avenue, Philadelphia, PA, 19111, USA.
Department of Pathology, Fox Chase Cancer Center, 333 Cottman Avenue, Philadelphia, PA, 19111, USA.
Methods Mol Biol. 2017;1579:245-255. doi: 10.1007/978-1-4939-6863-3_13.
The use of fluorescent probes in conjunction with white-light colonoscopy is a promising strategy for improving the detection of precancerous colorectal lesions, in particular flat (sessile) lesions that do not protrude into the lumen of the colon. We describe a method for determining the sensitivity and specificity of an enzymatically activated near-infrared probe (MMPSense680) for the detection of colon lesions in a mouse model (APC) of spontaneous colorectal cancer. Fluorescence intensity correlates directly with the activity of matrix metalloproteinases (MMPs). Overexpression of MMPs is an early event in the development of colorectal lesions. Although the probe employed serves as a reporter of the activity of MMPs, our method can be applied to any fluorescent probe that targets an early molecular event in the development of colorectal tumors.
将荧光探针与白光结肠镜检查相结合,是一种很有前景的策略,有助于提高结直肠癌前病变的检测率,尤其是那些不向结肠腔内突出的扁平(无蒂)病变。我们描述了一种方法,用于测定一种酶激活近红外探针(MMPSense680)在自发性结直肠癌小鼠模型(APC)中检测结肠病变的敏感性和特异性。荧光强度与基质金属蛋白酶(MMP)的活性直接相关。MMP的过表达是结直肠病变发展过程中的早期事件。虽然所使用的探针可作为MMP活性的报告分子,但我们的方法可应用于任何靶向结直肠肿瘤发生早期分子事件的荧光探针。