Armstrong Gemma R, Khot Mohammed I, Portal Christophe, West Nick P, Perry Sarah L, Maisey Tom I, Tiernan Jim P, Hughes Thomas A, Tolan Damian J, Jayne David G
Leeds Institute of Medical Research at St. James's, University of Leeds, Wellcome Trust Brenner Building, St James's University Hospital, Leeds, LS9 7TF, UK; Department of Colorectal Surgery, Leeds Teaching Hospitals NHS Trust, Leeds, LS9 7TF, UK.
Leeds Institute of Medical Research at St. James's, University of Leeds, Wellcome Trust Brenner Building, St James's University Hospital, Leeds, LS9 7TF, UK.
Surg Oncol. 2022 Mar;40:101679. doi: 10.1016/j.suronc.2021.101679. Epub 2021 Nov 20.
The c-Met protein is overexpressed in many gastrointestinal cancers. We explored EMI-137, a novel c-Met targeting fluorescent probe, for application in fluorescence-guided colon surgery, in HT-29 colorectal cancer (CRC) cell line and an in vivo murine model.
HT-29 SiRNA transfection confirmed specificity of EMI-137 for c-Met. A HT-29 CRC xenograft model was developed in BALB/c mice, EMI-137 was injected and biodistribution analysed through in vivo fluorescent imaging. Nine patients, received a single intravenous EMI-137 bolus (0.13 mg/kg), 1-3 h before laparoscopic-assisted colon cancer surgery (NCT03360461). Tumour and LN fluorescence was assessed intraoperatively and correlated with c-Met expression in eight samples by immunohistochemistry.
c-Met expression HT-29 cells was silenced and imaged with EMI-137. Strong EMI-137 uptake in tumour xenografts was observed up to 6 h post-administration. At clinical trial, no serious adverse events related to EMI-137 were reported. Marked background fluorescence was observed in all participants, 4/9 showed increased tumour fluorescence over background; 5/9 had histological LN metastases; no fluorescent LN were detected intraoperatively. All primary tumours (8/8) and malignant LN (15/15) exhibited high c-Met protein expression.
EMI-137, binds specifically to the human c-Met protein, is safe, and with further refinement, shows potential for application in fluorescence-guided surgery.
c-Met蛋白在许多胃肠道癌症中过度表达。我们探索了一种新型的靶向c-Met的荧光探针EMI-137,用于在HT-29结直肠癌(CRC)细胞系和体内小鼠模型中进行荧光引导的结肠手术。
HT-29细胞的SiRNA转染证实了EMI-137对c-Met的特异性。在BALB/c小鼠中建立了HT-29 CRC异种移植模型,注射EMI-137并通过体内荧光成像分析生物分布。9名患者在腹腔镜辅助结肠癌手术前1-3小时接受单次静脉注射EMI-137推注(0.13mg/kg)(NCT03360461)。术中评估肿瘤和淋巴结的荧光,并通过免疫组织化学与8个样本中的c-Met表达相关联。
HT-29细胞中的c-Met表达被沉默并用EMI-137成像。给药后6小时内观察到肿瘤异种移植中EMI-137的强烈摄取。在临床试验中,未报告与EMI-137相关的严重不良事件。在所有参与者中均观察到明显的背景荧光,4/9显示肿瘤荧光高于背景;5/9有组织学上的淋巴结转移;术中未检测到荧光淋巴结。所有原发性肿瘤(8/8)和恶性淋巴结(15/15)均表现出高c-Met蛋白表达。
EMI-137与人c-Met蛋白特异性结合,安全,经过进一步改进,显示出在荧光引导手术中的应用潜力。