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Intravital imaging of mouse colonic adenoma using MMP-based molecular probes with multi-channel fluorescence endoscopy

机译:使用基于MMP的分子探针和多通道荧光内窥镜对小鼠结肠腺瘤进行活体内成像

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Intravital imaging has provided molecular, cellular and anatomical insight into the study of tumor. Early detection and treatment of gastrointestinal (GI) diseases can be enhanced with specific molecular markers and endoscopic imaging modalities. We present a wide-field multi-channel fluorescence endoscope to screen GI tract for colon cancer using multiple molecular probes targeting matrix metalloproteinases (MMP) conjugated with quantum dots (QD) in AOM/DSS mouse model. MMP9 and MMP14 antibody (Ab)-QD conjugates demonstrate specific binding to colonic adenoma. The average target-to-background (T/B) ratios are 2.10 ± 0.28 and 1.78 ± 0.18 for MMP14 Ab-QD and MMP9 Ab-QD, respectively. The overlap between the two molecular probes is 67.7 ± 8.4%. The presence of false negative indicates that even more number of targeting could increase the sensitivity of overall detection given heterogeneous molecular expression in tumors. Our approach indicates potential for the screening of small or flat lesions that are precancerous.
机译:玻璃体内成像为肿瘤研究提供了分子,细胞和解剖学方面的见识。胃肠道(GI)疾病的早期发现和治疗可以通过特定的分子标记和内窥镜成像手段来增强。我们提出了一种宽视野的多通道荧光内窥镜,用于使用针对AOM / DSS小鼠模型中与量子点(QD)共轭的基质金属蛋白酶(MMP)的多种分子探针筛选结肠癌的胃肠道。 MMP9和MMP14抗体(Ab)-QD偶联物表现出与结肠腺瘤的特异性结合。 MMP14 Ab-QD和MMP9 Ab-QD的平均目标背景(T / B)比分别为2.10±0.28和1.78±0.18。两种分子探针之间的重叠率为67.7±8.4%。假阴性的存在表明,鉴于肿瘤中分子表达的异质性,甚至更多的靶向作用也可以提高整体检测的灵敏度。我们的方法表明了筛查癌前小或扁平病变的潜力。

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