首页> 外文期刊>Gastric cancer: official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association >New whole-body multimodality imaging of gastric cancer peritoneal metastasis combining fluorescence imaging with ICG-labeled antibody and MRI in mice
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New whole-body multimodality imaging of gastric cancer peritoneal metastasis combining fluorescence imaging with ICG-labeled antibody and MRI in mice

机译:结合胃癌荧光成像与ICG标记抗体和MRI的新型胃癌腹膜转移全身多模态成像

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Background: Peritoneal metastasis is the most frequent pattern of recurrence after curative surgery for gastric cancer. However, such a recurrence is difficult to detect by conventional computed tomography (CT) and magnetic resonance imaging (MRI) at an early stage. To improve the sensitivity and specificity of diagnostic imaging for peritoneal metastasis, we developed a new type of multimodality imaging combining fluorescence imaging with near-infrared fluorophore (NIR)-labeled antibodies and MRI. Methods: Dual optical imaging of peritoneal metastasis was carried out using luciferase-tagged gastric cancer cell lines and XenoLight CF750 or indocyanine green (ICG)-labeled anti-human epidermal growth factor receptor (EGFR) or CEA antibody as a probe in mice with Ivis in vivo imaging system. Results: This whole-body fluorescent imaging system sensitively detected metastatic foci <1 mm in diameter in the peritoneal cavity noninvasively. Fluorescence imaging proved to be specific because the fluorescence signal was abolished by blocking with excess unlabeled antibody. Although this fluorescence imaging had higher sensitivity for detection of small-sized peritoneal metastases than MRI, it proved difficult to accurately determine organ distribution of the metastasis. We thus developed a multimodality imaging system by the fusion of the three-dimensional fluorescence image with the MRI image and demonstrated its improved diagnostic accuracy over either method alone. Conclusion: The present results suggest that multimodality imaging consisting of fluorescence imaging with NIR-labeled EGFR or CEA antibody and MRI allows sensitive, specific, and anatomically accurate detection of peritoneal metastasis noninvasively at an early stage.
机译:背景:腹膜转移是胃癌根治性手术后最常见的复发方式。但是,这种复发很难在早期通过常规计算机断层扫描(CT)和磁共振成像(MRI)进行检测。为了提高诊断性影像学对腹膜转移的敏感性和特异性,我们开发了一种新型的多模态成像技术,将荧光成像技术与近红外荧光团(NIR)标记的抗体和MRI相结合。方法:使用荧光素酶标记的胃癌细胞系和XenoLight CF750或吲哚菁绿(ICG)标记的抗人表皮生长因子受体(EGFR)或CEA抗体作为腹膜转移的双光学成像技术,用于Ivis小鼠体内成像系统。结果:该全身荧光成像系统无创地检测了腹膜腔内直径小于1毫米的转移灶。荧光成像被证明是特异性的,因为通过用过量的未标记抗体阻断而消除了荧光信号。尽管此荧光成像比MRI具有更高的灵敏度,可检测出较小的腹膜转移,但难以准确确定转移的器官分布。因此,我们通过将三维荧光图像与MRI图像融合,开发了一种多模态成像系统,并证明了相对于任何一种方法,其诊断准确性都有所提高。结论:目前的结果表明,由NIR标记的EGFR或CEA抗体的荧光成像和MRI组成的多模态成像可在早期以无创方式对腹膜转移进行灵敏,特异性和解剖学准确的检测。

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