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使用CXCR4靶向示踪剂[Cu]Cu-NOTA-CP01对食管癌淋巴结转移进行体内检测

In Vivo Detection of Lymph Nodes Metastasis of ESCC Using CXCR4-Targeted Tracer [Cu]Cu-NOTA-CP01.

作者信息

Peng Tukang, Li Zhijun, Gao Jiebing, Yang Min, Qiu Yifan, Xian Jianzhong, Bi Lei, Ye Peizhen, Liu Yongshan, Jin Hongjun

机构信息

Guangdong Provincial Engineering Research Center of Molecular Imaging, The Fifth Affiliated Hospital, Sun Yat-sen University, Zhuhai, Guangdong Province, 519000, China.

Department of Urology, The Second Affiliated Hospital, Hengyang Medical School, University of South China, Hengyang, Hunan Province, 421001, China.

出版信息

Mol Imaging Biol. 2024 Dec;26(6):1046-1056. doi: 10.1007/s11307-024-01960-8. Epub 2024 Nov 4.

Abstract

PURPOSE

Esophageal squamous cell carcinoma (ESCC) frequently exhibits skip metastasis to lymph nodes; however, non-invasive imaging techniques capable of directly visualizing metastatic lymph nodes (MLN) are still lacking. Although biopsy is the clinical standard method, it is invasive and poses risks to patient health. This study aims to detect MLN in an intralymphatic tumor metastasis model of ESCC using the CXCR4-targeted tracer [Cu]Cu-NOTA-CP01.

PROCEDURES

The CXCR4 expression in ESCC cell lines was assessed using Western blot and immunofluorescence. An intralymphatic tumor metastasis model was established and monitored using bioluminescence imaging (BLI). Small animal PET studies and biodistribution studies were performed to evaluate the specificity of [Cu]Cu-NOTA-CP01 for MLN. Histopathology evaluation was employed to check for the presence of metastatic tumor cells and to assess CXCR4 expression levels in the metastatic lymph nodes.

RESULTS

The intralymphatic tumor metastasis model was successfully established using the EC109/Luc cell line, which exhibited high CXCR4 expression, as verified by BLI. PET/CT imaging showed that the MLN uptakes in the baseline group were significantly inhibited in the blocking group. The ratios of MLN/muscle and MLN/blood were also significantly higher in the baseline group than in the blocking group. Ex vivo PET/CT imaging of MLN corroborated the in vivo data. Biodistribution studies further supported the PET imaging studies, showing rapid clearance of the tracer from the blood and major organs, with significantly higher MLN/muscle and MLN/blood ratios in the baseline group compared to the blocking group. Histopathological staining verified positive CXCR4 expression in these lymph nodes containing metastatic tumor cells.

CONCLUSIONS

Targeting CXCR4 with [Cu]Cu-NOTA-CP01 for PET imaging of lymph nodes metastasis represents a promising approach that warrants further investigation. These findings have the potential to enhance diagnostic and therapeutic strategies for individuals with lymph nodes metastasis of ESCC.

摘要

目的

食管鳞状细胞癌(ESCC)常表现为跳跃式淋巴结转移;然而,仍缺乏能够直接可视化转移性淋巴结(MLN)的非侵入性成像技术。尽管活检是临床标准方法,但它具有侵入性,对患者健康构成风险。本研究旨在使用靶向CXCR4的示踪剂[Cu]Cu-NOTA-CP01在ESCC的淋巴管内肿瘤转移模型中检测MLN。

程序

使用蛋白质免疫印迹法和免疫荧光法评估ESCC细胞系中CXCR4的表达。建立淋巴管内肿瘤转移模型,并使用生物发光成像(BLI)进行监测。进行小动物PET研究和生物分布研究,以评估[Cu]Cu-NOTA-CP01对MLN的特异性。采用组织病理学评估来检查转移性肿瘤细胞的存在,并评估转移性淋巴结中CXCR4的表达水平。

结果

使用EC109/Luc细胞系成功建立了淋巴管内肿瘤转移模型,经BLI验证,该细胞系表现出高CXCR4表达。PET/CT成像显示,阻断组中基线组的MLN摄取明显受到抑制。基线组中MLN/肌肉和MLN/血液的比率也显著高于阻断组。MLN的离体PET/CT成像证实了体内数据。生物分布研究进一步支持了PET成像研究,显示示踪剂从血液和主要器官中快速清除,基线组中MLN/肌肉和MLN/血液的比率明显高于阻断组。组织病理学染色证实这些含有转移性肿瘤细胞的淋巴结中CXCR4表达呈阳性。

结论

用[Cu]Cu-NOTA-CP01靶向CXCR4进行淋巴结转移的PET成像代表了一种有前景的方法,值得进一步研究。这些发现有可能增强ESCC淋巴结转移患者的诊断和治疗策略。

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