Boonstra Martin C, van Driel Pieter B A A, van Willigen Danny M, Stammes Marieke A, Prevoo Hendrica A J M, Tummers Quirijn R J G, Mazar Andrew P, Beekman Freek J, Kuppen Peter J K, van de Velde Cornelis J H, Löwik Clemens W G M, Frangioni John V, van Leeuwen Fijs W B, Sier Cornelis F M, Vahrmeijer Alexander L
Department of Surgery, Leiden University Medical Center, Leiden, Netherlands.
Department of Radiology, Leiden University Medical Center, Leiden, Netherlands.
Oncotarget. 2015 Jun 10;6(16):14260-73. doi: 10.18632/oncotarget.3680.
Pre- and intraoperative diagnostic techniques facilitating tumor staging are of paramount importance in colorectal cancer surgery. The urokinase receptor (uPAR) plays an important role in the development of cancer, tumor invasion, angiogenesis, and metastasis and over-expression is found in the majority of carcinomas. This study aims to develop the first clinically relevant anti-uPAR antibody-based imaging agent that combines nuclear (111In) and real-time near-infrared (NIR) fluorescent imaging (ZW800-1). Conjugation and binding capacities were investigated and validated in vitro using spectrophotometry and cell-based assays. In vivo, three human colorectal xenograft models were used including an orthotopic peritoneal carcinomatosis model to image small tumors. Nuclear and NIR fluorescent signals showed clear tumor delineation between 24h and 72h post-injection, with highest tumor-to-background ratios of 5.0 ± 1.3 at 72h using fluorescence and 4.2 ± 0.1 at 24h with radioactivity. 1-2 mm sized tumors could be clearly recognized by their fluorescent rim. This study showed the feasibility of an uPAR-recognizing multimodal agent to visualize tumors during image-guided resections using NIR fluorescence, whereas its nuclear component assisted in the pre-operative non-invasive recognition of tumors using SPECT imaging. This strategy can assist in surgical planning and subsequent precision surgery to reduce the number of incomplete resections.
术前和术中有助于肿瘤分期的诊断技术在结直肠癌手术中至关重要。尿激酶受体(uPAR)在癌症发展、肿瘤侵袭、血管生成和转移中起重要作用,且在大多数癌症中存在过表达。本研究旨在开发首个基于抗uPAR抗体的具有临床相关性的成像剂,该成像剂结合了核素(111In)和实时近红外(NIR)荧光成像(ZW800-1)。使用分光光度法和基于细胞的试验在体外研究并验证了结合和结合能力。在体内,使用了三种人结直肠癌异种移植模型,包括原位腹膜癌模型以对小肿瘤进行成像。核素和近红外荧光信号在注射后24小时至72小时之间显示出清晰的肿瘤轮廓,使用荧光时在72小时的最高肿瘤与背景比值为5.0±1.3,使用放射性时在24小时为4.2±0.1。1-2毫米大小的肿瘤可通过其荧光边缘清晰识别。本研究表明,一种识别uPAR的多模态剂在使用近红外荧光的图像引导切除术中可视化肿瘤是可行的,而其核素成分有助于使用SPECT成像对肿瘤进行术前非侵入性识别。该策略可协助手术规划及后续精准手术,以减少不完全切除的数量。