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利用原位人器官oids对结肠腺瘤进行近红外体内成像以早期检测癌症

Near-Infrared Imaging of Colonic Adenomas In Vivo Using Orthotopic Human Organoids for Early Cancer Detection.

作者信息

Wu Xiaoli, Chen Chun-Wei, Jaiswal Sangeeta, Chang Tse-Shao, Zhang Ruoliu, Dame Michael K, Duan Yuting, Jiang Hui, Spence Jason R, Hsieh Sen-Yung, Wang Thomas D

机构信息

Division of Gastroenterology, Department of Internal Medicine, University of Michigan, Ann Arbor, MI 48109, USA.

Department of Gastroenterology and Hepatology, Linkou Chang Gung Memorial Hospital, Taoyuan 33305, Taiwan.

出版信息

Cancers (Basel). 2023 Sep 29;15(19):4795. doi: 10.3390/cancers15194795.

DOI:10.3390/cancers15194795
PMID:37835489
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10571995/
Abstract

Colorectal cancer is a leading cause of cancer-related morbidity and mortality worldwide. Premalignant lesions that are flat and subtle in morphology are often missed in conventional colonoscopies. Patient-derived adenoma colonoids with high and low cMet expression and normal colonoids were implanted orthotopically in the colon of immunocompromised mice to serve as a preclinical model system. A peptide specific for cMet was labeled with IRDye800, a near-infrared (NIR) fluorophore. This peptide was administered intravenously, and in vivo imaging was performed using a small animal fluorescence endoscope. Quantified intensities showed a peak target-to-background ratio at ~1 h after intravenous peptide injection, and the signal cleared by ~24 h. The peptide was stable in serum with a half-life of 3.6 h. Co-staining of adenoma and normal colonoids showed a high correlation between peptide and anti-cMet antibody. A human-specific cytokeratin stain verified the presence of human tissues implanted among surrounding normal mouse colonic mucosa. Peptide biodistribution was consistent with rapid renal clearance. No signs of acute toxicity were found on either animal necropsy or serum hematology and chemistries. Human colonoids provide a clinically relevant preclinical model to evaluate the specific uptake of a NIR peptide to detect premalignant colonic lesions in vivo.

摘要

结直肠癌是全球癌症相关发病和死亡的主要原因。形态扁平且不明显的癌前病变在传统结肠镜检查中常被漏诊。将具有高、低cMet表达的患者来源腺瘤类结肠组织以及正常类结肠组织原位植入免疫缺陷小鼠的结肠中,作为临床前模型系统。一种针对cMet的肽用近红外(NIR)荧光团IRDye800进行标记。该肽经静脉给药,并使用小动物荧光内窥镜进行体内成像。定量强度显示静脉注射肽后约1小时达到最高的靶标与背景比值,信号在约24小时后清除。该肽在血清中稳定,半衰期为3.6小时。腺瘤和正常类结肠组织的共染色显示该肽与抗cMet抗体之间具有高度相关性。人特异性细胞角蛋白染色证实了植入的人体组织存在于周围正常小鼠结肠黏膜中。肽的生物分布与肾脏快速清除一致。在动物尸检或血清血液学及生化检查中均未发现急性毒性迹象。人体类结肠组织为评估近红外肽在体内检测结肠癌前病变的特异性摄取提供了一个与临床相关且重要的临床前模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/749a/10571995/ff74275c2cbd/cancers-15-04795-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/749a/10571995/ecf2c2990a9c/cancers-15-04795-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/749a/10571995/f54224e17861/cancers-15-04795-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/749a/10571995/e4e32cbee2b1/cancers-15-04795-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/749a/10571995/5db28afa0b7c/cancers-15-04795-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/749a/10571995/8caea5829e0b/cancers-15-04795-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/749a/10571995/ff74275c2cbd/cancers-15-04795-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/749a/10571995/ecf2c2990a9c/cancers-15-04795-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/749a/10571995/f54224e17861/cancers-15-04795-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/749a/10571995/e4e32cbee2b1/cancers-15-04795-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/749a/10571995/5db28afa0b7c/cancers-15-04795-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/749a/10571995/8caea5829e0b/cancers-15-04795-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/749a/10571995/ff74275c2cbd/cancers-15-04795-g006.jpg

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