小鼠散发性和结肠炎相关结直肠癌中COX-2活性的内镜成像。

Diagnostic and Therapeutic Endoscopy Pub Date : 2013-01-01 Epub Date: 2013-01-15 DOI:10.1155/2013/250641
Sebastian Foersch, Clemens Neufert, Markus F Neurath, Maximilian J Waldner
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引用次数: 9

摘要

尽管几项研究提出阿司匹林对结直肠癌(CRC)的发展具有化学预防作用,但由于其不良副作用,不建议普遍使用阿司匹林。由于阿司匹林的保护作用与COX-2的表达增加有关,例如,在共聚焦内镜下对COX-2进行分子成像可以识别可能从阿司匹林治疗中受益的患者。在这项试点试验中,我们使用cox -2特异性荧光探针在共聚焦显微镜下检测小鼠结肠炎相关和散发性结直肠癌。将COX-2探针注射到携带肿瘤的APCmin小鼠或暴露于AOM + DSS结肠炎相关癌模型的小鼠体内,可通过体内荧光成像验证COX-2的肿瘤特异性上调。随后的肿瘤组织共聚焦成像显示,与健康对照组的正常粘膜相比,表达COX-2的细胞数量增加。cox -2在肿瘤细胞和浸润间质细胞中的表达可通过亚细胞分辨率检测。这些发现提出了一个概念的证明,并建议使用CLE检测结肠直肠癌内窥镜监测期间COX-2的表达。这可以改善结直肠癌患者的早期发现和化学预防分层。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Endomicroscopic Imaging of COX-2 Activity in Murine Sporadic and Colitis-Associated Colorectal Cancer.

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.

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